|Publication number||US20050171044 A1|
|Application number||US 11/022,358|
|Publication date||Aug 4, 2005|
|Filing date||Dec 22, 2004|
|Priority date||Dec 24, 2003|
|Also published as||CA2550642A1, CA2550642C, EP1704243A2, EP1704243A4, EP1704243B1, US8759307, US20070037763, US20090012280, US20150126722, WO2005065268A2, WO2005065268A3|
|Publication number||022358, 11022358, US 2005/0171044 A1, US 2005/171044 A1, US 20050171044 A1, US 20050171044A1, US 2005171044 A1, US 2005171044A1, US-A1-20050171044, US-A1-2005171044, US2005/0171044A1, US2005/171044A1, US20050171044 A1, US20050171044A1, US2005171044 A1, US2005171044A1|
|Inventors||David Stein, Richard Bestwick, Patrick Iversen, Benjamin Neuman, Michael Buchmeier|
|Original Assignee||Stein David A., Bestwick Richard K., Iversen Patrick L., Benjamin Neuman, Michael Buchmeier|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (6), Referenced by (8), Classifications (18), Legal Events (3)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This patent application claims priority to U.S. Provisional Application No. 60/532,701 filed on Dec. 24, 2003, which is incorporated herein in its entirety by reference.
This invention relates to an oligonucleotide analog for use in treating in animals a coronavirus infection or, more generally, an infection by a member of the Nidovirales order, to an antiviral method employing the analog, and to a method for monitoring binding of the analog to a viral genome target site.
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The Nidovirales is a recently established order comprising the families Arteriviridae (genus Afterivirus) and Coronaviridae (genera Coronavirus and Torovirus). Despite noteworthy differences in genome size, complexity and virion architecture, coronaviruses, toroviruses and arteriviruses are remarkably similar in genome organization and replication strategy (de Vries, Horzinek et al. 1997). The name Nidovirales is derived from the Latin nidus, to nest, and refers to the 3′ coterminal nested set of subgenomic (sg) viral mRNAs produced during infection. Sequence comparisons of the replicase genes suggest that the Nidovirales have evolved from a common ancestor despite their substantial differences.
Coronaviruses cause about 30% of common colds in humans and, unlike rhinoviruses, cause both upper and lower respiratory infections, the latter being a more serious affliction. In addition, coronaviruses cause gastroenteritis and diarrhea in humans and many other serious diseases in non-human animals including mice, chickens, pigs and cats. Although no known human arteriviruses exist, arteriviruses cause a number of diseases in horses, pigs, mice and monkeys.
The most well-known human coronavirus has only recently appeared and is responsible for severe acute respiratory syndrome (SARS), a life threatening form of pneumonia (Peiris, Yuen et al. 2003). SARS is caused by a previously unknown coronavirus named SARS coronavirus (SARS-CoV). First appearing in November 2002, an epidemic emerged that spread from its zoonotic origin in Guangdong Province, China, to 26 countries on five continents. By August 2003, a cumulative total of 8422 cases and 774 deaths had been recorded by the World Health Organization. The rapid transmission by aerosols and the fecal-oral route and the high mortality rate (11%) make SARS a potential global threat for which no efficacious therapy is available.
No vaccines for coronaviruses or arteriviruses (Nidoviruses) are available and no effective antiviral therapies are available to treat an infection. As with many other human viral pathogens, available treatment involves supportive measures such as anti-pyretics to keep fever down, fluids, antibiotics for secondary bacterial infections and respiratory support as necessary.
In view of the severity of the diseases caused by Nidoviruses and the lack of effective prevention or therapies, it is therefore an object of the present invention to provide therapeutic compounds and methods for treating a host infected with a coronavirus, torovirus or arterivirus.
In one aspect, the invention includes an oligonucleotide compound for use in inhibiting replication of a nidovirus in human cells. The compound is characterized by: (i) a nuclease-resistant backbone, (ii) capable of uptake by virus-infected human cells, (iii) containing between 8-25 nucleotide bases, and (iv) having a sequence that is complementary to at least 8 bases contained in one of:
The compound is capable of forming with the nidovirus (1) positive-strand genomic RNA or (2) the negative-strand 3′ subgenomic region, a heteroduplex structure characterized by (1) a Tm of dissociation of at least 45° C., and (2) a disrupted base pairing between the transcriptional regulatory sequences in the 5′ leader region of the positive-strand viral genome and negative-strand 3′ subgenomic region.
The compound may be composed of morpholino subunits and phosphorus-containing intersubunit linkages joining a morpholino nitrogen of one subunit to a 5′ exocyclic carbon of an adjacent subunit. Exemplary intersubunit linkages are phosphorodiamidate linkages in accordance with the structure:
In one general embodiment, the compound has a sequence complementary to at least 8 bases contained in the 5′ leader sequence of the nidovirus' positive-strand genomic RNA from the group SEQ ID NOS: 1-9. The compound sequence is preferably complementary to at least a portion of the transcriptional regulatory sequence contained within one of the sequences SEQ ID NOS: 1-9. Exemplary compound sequences in this embodiment include SEQ ID NOS: 20-35.
For use in inhibiting replication of human SARS virus, the compound may contain one of sequences SEQ ID NOS: 26 and 27. For use in inhibiting replication of human coronavius-229E or human coronavirus-OC43, the compound may contain one of the sequences SEQ ID NOS: 22 or 23, for the coronavirus-229E, and the sequence SEQ ID NOS: 24 or 25, for the coronavirus-OC43. For use in inhibiting replication of feline coronavirus, the compound may contain SEQ ID NOS: 20 or 21.
In another general embodiment, the compound has a sequence complementary to at least 8 bases contained in the negative-strand 3′ subgenomic region of the virus exemplified by the group SEQ ID NOS: 10-19. The compound preferably has a sequence complementary to at least a portion of the minus-strand body transcriptional regulatory sequence contained within one of the sequences SEQ ID NOS: 10-19. Exemplary compound sequences in this embodiment contain a sequence from the group SEQ ID NOS: 36-45.
For use in inhibiting replication of human SARS virus, the compound may contain one of the sequences SEQ ID NOS: 36-43. For use in inhibiting replication of simian hemorrhagic fever virus, the compound may contain the SEQ ID NOS: 44 and 45.
In the method of the invention for inhibiting nidovirus replication in virus-infected cells, the cells are exposed to the oligonucleotide compound, in an amount sufficient to inhibit nidovirus replication in the virus-infected cells. The inhibition is due to base-pair binding of the compound to (1) a sequence in a 5′ leader sequence of the nidovirus' positive-strand genomic RNA that includes an internal leader transcriptional regulatory sequence, or (2) a sequence in a negative-strand 3′ subgenomic region of the virus that includes an internal body transcriptional regulatory sequence that is substantially complementary to the corresponding transcriptional regulatory sequence contained the 5′ leader sequence. This base-pair binding forms a viral-RNA/compound heteroduplex characterized by (1) a Tm of dissociation of at least 45° C., and (2) a disrupted base pairing between the transcriptional regulatory sequences in the 5′ leader region of the positive-strand viral genome and negative-strand 3′ subgenomic region. Various embodiments of the compound, noted above, are incorporated into the method.
For use in treating a nidovirus infection in a human or veterinary-animal subject, the compound may be administered orally to the subject, to contact the compound with the virus-infected cells. The method may further include monitoring a subject body fluid for the appearance of a heteroduplex composed of the oligonucleotide compound and a complementary portion of the viral genome in positive- or negative-strand form.
These and other objects and features of the invention will become more fully apparent when the following detailed description of the invention is read in conjunction with the accompanying drawings.
The terms below, as used herein, have the following meanings, unless indicated otherwise:
The terms “oligonucleotide analog” refers to oligonucleotide having (i) a modified backbone structure, e.g., a backbone other than the standard phosphodiester linkage found in natural oligo- and polynucleotides, and (ii) optionally, modified sugar moieties, e.g., morpholino moieties rather than ribose or deoxyribose moieties. The analog supports bases capable of hydrogen bonding by Watson-Crick base pairing to standard polynucleotide bases, where the analog backbone presents the bases in a manner to permit such hydrogen bonding in a sequence-specific fashion between the oligonucleotide analog molecule and bases in a standard polynucleotide (e.g., single-stranded RNA or single-stranded DNA). Preferred analogs are those having a substantially uncharged, phosphorus containing backbone.
A substantially uncharged, phosphorus containing backbone in an oligonucleotide analog is one in which a majority of the subunit linkages, e.g., between 60-100%, are uncharged at physiological pH, and contain a single phosphorous atom. The analog contains between 8 and 40 subunits, typically about 8-25 subunits, and preferably about 12 to 25 subunits. The analog may have exact sequence complementarity to the target sequence or near complementarity, as defined below.
A “subunit” of an oligonucleotide analog refers to one nucleotide (or nucleotide analog) unit of the analog. The term may refer to the nucleotide unit with or without the attached intersubunit linkage, although, when referring to a “charged subunit”, the charge typically resides within the intersubunit linkage (e.g. a phosphate or phosphorothioate linkage).
A “morpholino oligonucleotide analog” is an oligonucleotide analog composed of morpholino subunit structures of the form shown in
The subunit and linkage shown in
A preferred morpholino oligomer is a phosphorodiamidate-linked morpholino oligomer, referred to herein as a PMO. Such oligomers are composed of morpholino subunit structures such as shown in
The term “substituted”, particularly with respect to an alkyl, alkoxy, thioalkoxy, or alkylamino group, refers to replacement of a hydrogen atom on carbon with a heteroatom-containing substituent, such as, for example, halogen, hydroxy, alkoxy, thiol, alkylthio, amino, alkylamino, imino, oxo (keto), nitro, cyano, or various acids or esters such as carboxylic, sulfonic, or phosphonic. It may also refer to replacement of a hydrogen atom on a heteroatom (such as an amine hydrogen) with an alkyl, carbonyl or other carbon containing group.
As used herein, the term “target”, relative to the viral genomic RNA, refers to a viral genomic RNA, and may include either the positive strand RNA which is the replicative strand of the virus, or the negative or antisense strand which is formed in producing multiple new copies of the positive-strand RNA.
The term “target sequence” refers to a portion of the target RNA against which the oligonucleotide analog is directed, that is, the sequence to which the oligonucleotide analog will hybridize. The target sequence includes at least a portion of one of the sequences identified as SEQ ID NOS: 1-9, representing the genome's leader transcriptional regulatory sequence in a member of the Nidovirales, as discussed further below. Another target sequence includes at least a portion of the 3′ minus-strand body transcriptional regulatory sequence exemplified by SEQ ID NOS: 10-19.
The term “targeting sequence” is the sequence in the oligonucleotide analog that is complementary or substantially complementary to the target sequence in the RNA genome. The entire sequence, or only a portion of, the analog may be complementary to the target sequence, or only a portion of the total analog sequence. For example, in an analog having 20 bases, only 8-12 may be targeting sequences. Typically, the targeting sequence is formed of contiguous bases in the analog, but may alternatively be formed of non-contiguous sequences that when placed together, e.g., from opposite ends of the analog, constitute sequence that spans the target sequence. As will be seen, the target and targeting sequences are selected such that binding of the analog to part of the viral genome acts to disrupt or prevent formation of subgenomic RNA formed by the interaction between leader and body transcriptional regulatory sequences.
Target and targeting sequences are described as “complementary” to one another when hybridization occurs in an antiparallel configuration. A double-stranded polynucleotide can be “complementary” to another polynucleotide. A targeting sequence may have “near” or “substantial” complementarity to the target sequence and still function for the purpose of the present invention. Preferably, the oligonucleotide analogs employed in the present invention have at most one mismatch with the target sequence out of 10 nucleotides, and preferably at most one mismatch out of 20. Alternatively, the antisense oligomers employed have at least 90% sequence homology, and preferably at least 95% sequence homology, with the exemplary targeting sequences as designated herein.
An oligonucleotide analog “specifically hybridizes” to a target polynucleotide if the oligomer hybridizes to the target under physiological conditions, with a Tm substantially greater than 45° C., preferably at least 50° C., and typically 60° C.-80° C. or higher. Such hybridization preferably corresponds to stringent hybridization conditions. At a given ionic strength and pH, the Tm is the temperature at which 50% of a target sequence hybridizes to a complementary polynucleotide. Again, such hybridization may occur with “near” or “substantial” complementary of the antisense oligomer to the target sequence, as well as with exact complementarity.
A “nuclease-resistant” oligomeric molecule (oligomer) refers to one whose backbone is substantially resistant to nuclease cleavage, in non-hybridized or hybridized form; by common extracellular and intracellular nucleases in the body; that is, the oligomer shows little or no nuclease cleavage under normal nuclease conditions in the body to which the oligomer is exposed.
A “heteroduplex” refers to a duplex between an oligonculeotide analog and the complementary portion of a target RNA. A “nuclease-resistant heteroduplex” refers to a heteroduplex formed by the binding of an antisense oligomer to its complementary target, such that the heteroduplex is substantially resistant to in vivo degradation by intracellular and extracellular nucleases, such as RNAseH, which are capable of cutting double-stranded RNA/RNA or RNA/DNA complexes.
A “base-specific intracellular binding event involving a target RNA” refers to the specific binding of an oligonucleotide analog to a target RNA sequence inside a cell. The base specificity of such binding is sequence specific. For example, a single-stranded polynucleotide can specifically bind to a single-stranded polynucleotide that is complementary in sequence.
An “effective amount” of an antisense oligomer, targeted against an infecting ssRNA virus, is an amount effective to reduce the rate of replication of the infecting virus, and/or viral load, and/or symptoms associated with the viral infection.
As used herein, the term “body fluid” encompasses a variety of sample types obtained from a subject including, urine, saliva, plasma, blood, spinal fluid, or other sample of biological origin, such as skin cells or dermal debris, and may refer to cells or cell fragments suspended therein, or the liquid medium and its solutes.
The term “relative amount” is used where a comparison is made between a test measurement and a control measurement. The relative amount of a reagent forming a complex in a reaction is the amount reacting with a test specimen, compared with the amount reacting with a control specimen. The control specimen may be run separately in the same assay, or it may be part of the same sample (for example, normal tissue surrounding a malignant area in a tissue section).
“Treatment” of an individual or a cell is any type of intervention provided as a means to alter the natural course of the individual or cell. Treatment includes, but is not limited to, administration of e.g., a pharmaceutical composition, and may be performed either prophylactically, or subsequent to the initiation of a pathologic event or contact with an etiologic agent. The related term “improved therapeutic outcome” relative to a patient diagnosed as infected with a particular virus, refers to a slowing or diminution in the growth of virus, or viral load, or detectable symptoms associated with infection by that particular virus.
An agent is “actively taken up by mammalian cells” when the agent can enter the cell by a mechanism other than passive diffusion across the cell membrane. The agent may be transported, for example, by “active transport”, referring to transport of agents across a mammalian cell membrane by e.g. an ATP-dependent transport mechanism, or by “facilitated transport”, referring to transport of antisense agents across the cell membrane by a transport mechanism that requires binding of the agent to a transport protein, which then facilitates passage of the bound agent across the membrane. For both active and facilitated transport, the oligonucleotide analog preferably has a substantially uncharged backbone, as defined below. Alternatively, the antisense compound may be formulated in a complexed form, such as an agent having an anionic backbone complexed with cationic lipids or liposomes, which can be taken into cells by an endocytotic mechanism. The analog may be conjugated, e.g., at its 5′ or 3′ end, to an arginine rich peptide, e.g., the HIV TAT protein, or polyarginine, to facilitate transport into the target host cell.
The term “coronavirus” is used herein to include all members of the Coronaviridae family including viruses of the Coronavirus and Torovirus genera. The term “arterivirus” includes members of the Arteriviridae family which includes the Arterivirus genera. The term “Nidovirus” refers to viruses of the Nidovirales order which includes the families Coronaviridae and Arteriviridae. Representative Nidoviruses are listed in Table 1. below.
TABLE 1 Representative Nidoviruses Virus Name Abbreviation Canine coronavirus CCoV Feline coronavirus FCoV Human coronavirus 229E HCoV-229E Porcine epidemic diarrhea virus PEDV Transmissible gastroenteritis virus TGEV Porcine Respiratory Coronavirus PRCV Bovine coronavirus BCoV Human coronavirus OC43 HCoV-OC43 Murine hepatitis virus MHV Rat coronavirus RCV Infectious bronchitis virus IBV Turkey coronavirus TCoV Rabbit coronavirus RbCoV SARS coronavirus SARS-CoV Human torovirus HuTV Equine arteritis virus EAV Porcine reproductive and respiratory syndrome virus PRRSV Porcine hemagglutinating encephalomyelitis virus PHEV Simian hemorrhagic fever virus SHFV
II. Target Coronaviruses and Arteriviruses
The present invention is based on the discovery that effective inhibition of coronavirus replication can be achieved by exposing coronavirus-infected cells to oligomeric analogs (i) targeted to the transcriptional regulatory sequence (TRS) region of coronavirus RNA and (ii) having physical and pharmacokinetic features which allow effective interaction between the analog and the viral RNA within host cells. In one aspect, the analogs can be used in treating a mammalian subject infected with the virus.
The invention targets members of the Coronaviridae and Arteriviridae families of the Nidovirales order including, but not limited to, the viruses described below. Various physical, morphological, and biological characteristics of the genes, and members therein, can be found, for example, in (Strauss and Strauss 2002), and in one or more of the references cited herein. Some of the key biological, pathological and epidemiological characteristics of representative nidoviruses are summarized below. Recent reviews on coronaviruses are available (e.g. see (Siddell 1995; Lai and Cavanagh 1997) and are incorporated herein in their entirety.
A. Human Coronaviruses
Coronaviruses are known to cause approximately 30% of common colds in humans. The most studied of these are human coronaviruses HCoV-229E and HCoV-OC43. These viruses are spread by the respiratory route and, unlike rhinoviruses, cause both upper and lower respiratory tract infections. Lower respiratory tract infections are considered more serious clinically. In addition to these viruses, human torovirus (HuTV) causes gastroenteritis and diarrhea in infected individuals.
The SARS-CoV causes a life-threatening form of pneumonia called severe acute respiratory syndrome (SARS). From its likely zoonotic origin in Guangdong Province, China in November 2002, the SARS-CoV spread rapidly to 29 countries, infected over 8400 individuals and caused more than 750 deaths (Peiris, Yuen et al. 2003). The rapid transmission by aerosols and probably the fecal-oral route coupled with the high mortality rate make SARS a global threat for which no efficacious therapy is available. There is evidence that natural infection with SARS-CoV occurs in a number of animal species indigenous to China and parts of southeast Asia (Guan, Zheng et al. 2003). Genome sequences of SARS-CoV isolates obtained from a number of index patients have been published recently (Marra, Jones et al. 2003; Rota, Oberste et al. 2003). A virus closely related genetically to SARS-CoV was isolated from several animals obtained from a market in Quangdong Province. Sequencing of the viruses obtained from these animals demonstrated that the most significant difference between them and SARS-CoV was an additional 29 base-pair sequence in the animal viruses. The role of animals in the transmission of SARS-CoV to humans and whether an animal reservoir for the virus exists is the subject of active, ongoing research.
B. Animal Coronaviruses and Arteriviruses
Coronaviruses and Arteriviruses for many other animals are known, including mice chickens, pigs, and cats. Associated diseases include respiratory disease, gastroenteritis, hepatitis, and a syndrome similar to multiple sclerosis of humans, among many other illnesses. Mouse hepatitis virus (MHV) has been particularly well studied and, along with the Arterivirus equine arteritis virus (EAV) has been the prototypic molecular model system for the Nidovirales order.
One animal coronavirus that causes significant animal mortality is feline infectious peritonitis virus, the leading cause of death in young domestic cats. The feline coronaviruses (FCoV) generally do not cause infections with high morbidity but in a small percentage of cases, the virus mutates to become more virulent. This virus, feline infectious peritonitis virus (FIPV), causes severe disease in young cats. This disease is in large part immunopathological and understanding it is a major goal of coronavirus research. The infection causes lesions in many organs, most prominently in the liver and spleen. The disease is further characterized by disseminated inflammation and serositis in the abdominal and thoracic cavities. In addition to this “wet” or effusive form, a “dry” or noneffusive form of feline infectious peritonitis (FIP) also occurs. Both forms are different manifestations of the same infection. Despite many studies, the pathogenesis of FIP is still not well understood.
Another serious non-human Nidovirus is porcine reproductive and respiratory syndrome virus (PRRSV), an arterivirus similar to EAV and SHFV. The disease caused by PRRSV causes reproductive failure in sows, pre-weaning mortality and respiratory tract illness that can have severe consequences, especially in piglets (Allende, Lewis et al. 1999). This virus causes significant losses in the pig industry with associated economic ramifications.
III. Coronavirus and Arterivirus Replication and Gene Expression
Coronaviruses encode an RNA genome that is capped, polyadenylated, nonsegmented, infectious, positive-strand, approximately 30 kb and considered the largest of all known viral RNA genomes. Arteriviruses have a 13 kb genome that is very similar in organization and expression strategy to that of coronaviruses. The 5′ two-thirds of the coronavirus genome is occupied by the open reading frame (ORF) 1a and ORF 1b which encode the replicase proteins of the virus. These genes are translated from infecting genomic RNA into two polyprotein precursors which produce the viral replication and transcription functions. Downstream of ORF 1b a number of genes occur that encode structural and several nonstructural, accessory proteins. These genes are expressed through a 3′-coterminal nested set of subgenomic mRNAs (sg mRNAs) that are synthesized by a process of discontinuous transcription. The sg mRNAs represent variable lengths of the 3′ end of the viral genome, each one provided at its 5′ end with a sequence identical to the genomic 5′ “leader” sequence. The mRNAs are each functionally monocistronic (i.e. the proteins are translated only from the 5′-most ORF). A schematic that illustrates the gene organization and sg mRNAs of SARS-CoV is shown in
The control of gene expression by discontinuous transcription is novel and unique to a small number of single stranded RNA viruses, most notably the Nidovirales order (de Vries, Horzinek et al. 1997).
The fusion of the noncontiguous sequences during discontinuous transcription is believed to be achieved through the involvement of transcriptional regulatory sequences (TRSs). The TRS sequences are short, 6-12 nucleotide regions that are found at the 3′ end of the leader sequence (leader TRS), and upstream of the genes in the 3′-proximal part of the genome (body TRSs). The TRSs are homologous and are believed to function by a mechanism where the minus-strand body TRS “jumps” to the complementary leader TRS on the positive-sense strand where it “lands” (i.e., the two TRSs hybridize) allowing completion of the synthesis of the negative-sense leader sequence (i.e., see
IV. Antisense Targeting of Nidovirus Transcriptional Regulatory Sequences
The preferred target sequences are those nucleotide sequences adjacent and including at least a portion, e.g., at least 2-8 bases, of the leader TRS of the positive-RNA or the minus-strand body TRS of Nidovirus RNA. As discussed above, the TRSs appear to play a critical role in viral transcription by bringing into close proximity the minus-strand body TRS and positive-strand leader TRS in order to complete synthesis of the negative-sense sg RNA templates.
A variety of Nidovirus genome sequences are available from well known sources, such as the NCBI Genbank databases. Alternatively, a person skilled in the art can find sequences for many of the subject viruses in the open literature, e.g., by searching for references that disclose sequence information on designated viruses. Once a complete or partial viral sequence is obtained, the leader TRS sequence of the virus is identified.
GenBank references for exemplary viral nucleic acid sequences containing the leader TRS or body TRS in the corresponding viral genomes are listed in Table 2 below. It will be appreciated that these sequences are only illustrative of other Nidovirus sequences, as may be available from available gene-sequence databases or literature or patent resources. The sequences below, identified as SEQ ID NOs 1-19, are also listed in Table 4 at the end of the specification. The bold nucleotides in Table 2 identify the core leader TRS or the body minus-strand TRS.
TABLE 2 Exemplary TRS Target Sequences GenBank Leader SEQ Virus Acc. No. TRS Ncts. ID NO. Target Sequence (5′ to 3′) FCoV AY204705 109-135 1 cggacaccaacucgaacuaaacgaaau TGEV AJ271965 78-104 2 cggacaccaacucgaacuaaacgaaau HCoV-229E AF304460 55-78 3 cuacuuuucucaacuaaacgaaau HCoV-OC43 AY391777 51-74 4 gaucuuuuuguaaucuaaacuuua SARS-CoV AY274119 53-76 5 gaucuguucucuaaacgaacuuua MHV AF029248 50-75 6 guaguuuaaaucuaaucuaaacuuua SHFV AF180391 188-215 7 gauuugcagacccuccuuaaccauguuc PRRSV AF046869 168-194 8 cggucucuccaccccuuuaaccauguc EAV X53459 189-228 9 caucgucgucgaucucuaucaacuaccc uugcgacuaugg GenBank Body Minus- SEQ Target Sequence Virus Acc. No. Strand TRS Ncts. ID NO. (5′ to 3′ - minus strand) SARS-CoV AY291315 21482-21502 10 aaaauaaacauguucguuuag SARS-CoV AY291315 25257-25277 11 acaaauccauaaguucguuua SARS-CoV AY291315 26109-26129 12 cgaaugaguacauaaguucgu SARS-CoV AY291315 26343-26363 13 auaauaguuaguucguuuaga SARS-CoV AY291315 26913-26933 14 uuguaauaagaaagcguucgu SARS-CoV AY291315 27265-27285 15 gaauaauuuucauguucguuu SARS-CoV AY291315 27768-27788 16 gaaguuucauguucguuuaga SARS-CoV AY291315 28103-28123 17 acauuuuaauuuguucguuua SHFV AF180391 14699-14719 18 ucagcacgucgucgugguuga SHFV AF180391 15280-15300 19 agccauacuuccucagguuaa
The degree of complementarity between the target and targeting sequence is sufficient to form a stable duplex. The region of complementarity of the antisense oligomers with the target RNA sequence may be as short as 8-11 bases, but is preferably 12-15 bases or more, e.g. 12-20 bases, or 12-25 bases. An antisense oligomer of about 15 bases is generally long enough to have a unique complementary sequence in the viral genome. In addition, a minimum length of complementary bases may be required to achieve the requisite binding Tm, as discussed below.
Oligomers as long as 40 bases may be suitable, where at least the minimum number of bases, e.g., 8-11 and preferably 12-15 bases, are complementary to the target sequence. In general, however, facilitated or active uptake in cells is optimized at oligomer lengths less than about 30, preferably less than 25, and more preferably 20 or fewer bases. For PMOs, described further below, an optimum balance of binding stability and uptake generally occurs at lengths of 13-23 bases.
The oligomer may be 100% complementary to the viral nucleic acid target sequence, or it may include mismatches, e.g., to accommodate variants, as long as a heteroduplex formed between the oligomer and viral nucleic acid target sequence is sufficiently stable to withstand the action of cellular nucleases and other modes of degradation which may occur in vivo. Oligomer backbones which are less susceptible to cleavage by nucleases are discussed below. Mismatches, if present, are less destabilizing toward the end regions of the hybrid duplex than in the middle. The number of mismatches allowed will depend on the length of the oligomer, the percentage of G:C base pairs in the duplex, and the position of the mismatch(es) in the duplex, according to well understood principles of duplex stability. Although such an antisense oligomer is not necessarily 100% complementary to the viral nucleic acid target sequence, it is effective to stably and specifically bind to the target sequence, such that a biological activity of the nucleic acid target, e.g. discontinous transcription, is modulated.
The stability of the duplex formed between the oligomer and the target sequence is a function of the binding Tm and the susceptibility of the duplex to cellular enzymatic cleavage. The Tm of an antisense compound with respect to complementary-sequence RNA may be measured by conventional methods, such as those described by Hames et al., Nucleic Acid Hybridization, IRL Press, 1985, pp.107-108. Each antisense oligomer should have a binding Tm, with respect to a complementary-sequence RNA, of greater than body temperature and preferably greater than 45° C. Tm's in the range 60-80° C. or greater are preferred. According to well known principles, the Tm of an oligomer compound, with respect to a complementary-based RNA hybrid, can be increased by increasing the ratio of C:G paired bases in the duplex, and/or by increasing the length (in base pairs) of the heteroduplex. At the same time, for purposes of optimizing cellular uptake, it may be advantageous to limit the size of the oligomer. For this reason, compounds that show high Tm (50° C. or greater) at a length of 15 bases or less are generally preferred over those requiring 20+ bases for high Tm values.
Table 3 below lists exemplary targeting sequences directed against the leader TRS or minus-strand body TRS for selected Nidoviruses. These sequences, identified by SEQ ID NOS: 20-46, are complementary and antiparallel to the target sequences identified as SEQ ID NOS: 1-19 above. As noted above, the actual targeting sequence in the oligonucleotide analog may be complementary to only a portion of the corresponding target sequence in Table 2.
More generally, the invention contemplates, as exemplary targeting sequences, a sequence of at least 8 bases complementary to a region of the virus' positive-strand RNA genome that includes at least a portion of the genome's positive-strand leader TRS. In addition, exemplary targeting sequences are sequences of at least 8 bases complementary to a region of the virus' negative strand that includes at least a portion of the genome's negative-strand body TRS. The targeting sequence contains a sufficient number of bases in either of the TRSs to disrupt base pairing between the virus leader and body TRS sequences. The number of targeting sequences needed to disrupt this structure is preferably at least 2-4 bases complementary to the core leader or body TRS (shown in bold in Table 2), plus bases complementary to adjacent target-sequence bases.
The exemplary targeting sequences in Table 3 below and target sequences in Table 2 for minus-strand body TRSs correspond to individual subgenomic messenger RNAs (sg mRNAs). For SARS-CoV, sg mRNA targets and targeting sequences for mRNA2 through mRNA9 correspond to SEQ ID NOS: 10-17 and SEQ ID NOS: 36-43, respectively (Thiel, Ivanov et al. 2003). For SHFV, sg mRNAs targets and targeting sequences for mRNA 6 and 7 correspond to SEQ ID NOS: 18 and 19 and SEQ ID NOS: 44 and 45, respectively (Zeng, Godeny et al. 1995).
TABLE 3 Exemplary Targeting Sequences Against the Leader TRS of Nidoviruses GenBank Leader TRS SEQ Virus(es) Acc. No. Targeting Sequences (5′ to 3′) ID NO. FCoV AY204705 ATTTCGTTTAGTTCGAGTTGGGTTTAGTT 20 TGEV AJ271965 CGAGTTGGTGTCCG 21 CaCoV N/A PRCV X52668 HCoV-229E AF304460 ATTTCGTTTAGTTGAGAAAAGGTTTAGTT 22 GAGAAAAGTAG 23 HCoV-OC43 AY391777 TAAAGTTTAGATTACAAAAAGGTTTAGAT 24 BCoV AF220295 TACAAAAAGATC 25 PHEV AF523845 SARS-CoV AY274119 TAAAGTTCGTTTAGAGAACAGGTTCGTT 26 TAGAGAACAGATC 27 MHV AF029248 TAAAGTTTAGATTAGATTTAAACGTTTAG 28 ATTAGATTTAAACTAC 29 SHFV AF180391 GAACATGGTTAAGGAGGGTCTGGGTTA 30 AGGAGGGTCTGCAAATC 31 PRRSV AF046869 GACATGGTTAAAGGGGTGGAGGGTTAA 32 AGGGGTGGAGAGACCG 33 EAV X53459 GGGTAGTTGATAGAGATCGACGAGTTG 34 ATAGAGATCGACGACGATGCCATAGTC 35 GCAAGGGTAGTTGA 46 SARS-CoV AY274119 CTAAACGAACATGTTTATTTT 36 SARS-CoV AY274119 TAAACGAACTTATGGATTTGT 37 SARS-CoV AY274119 ACGAACTTATGTACTCATTCG 38 SARS-CoV AY274119 TCTAAACGAACTAACTATTAT 39 SARS-CoV AY274119 ACGAACGCTTTCTTATTACAA 40 SARS-CoV AY274119 AAACGAACATGAAAATTATTC 41 SARS-CoV AY274119 TCTAAACGAACATGAAACTTC 42 SARS-CoV AY274119 TAAACGAACAAATTAAAATGT 43 SHFV AF180391 TCAACCACGACGACGTGCTGA 44 SHFV AF180391 TTAACCTGAGGAAGTATGGCT 45
Note that the target sequence in Table 3 is indicated as containing uracil (U) bases characteristic of RNA, and the targeting sequences in Table 3, as containing thymine bases characteristic of DNA. It will be understood that the targeting sequence bases may be normal DNA bases or analogs thereof, e.g., uracil, that are capable of Watson-Crick base pairing to target-sequence RNA bases. Also note that where more than one virus is listed for any given targeting sequence, there is sufficient sequence homology for the targeting sequences to effectively hybridize to those viral targets.
IV. Antisense Oligomers
As detailed above, the antisense oligomer has a base sequence directed to a targeted portion of the viral genome, preferably the leader TRS and adjacent nucleotides. In addition, the oligomer is able to effectively target infecting viruses, when administered to an infected host cell, e.g. in an infected animal subject. This requirement is met when the oligomer compound (a) has the ability to be actively taken up by mammalian cells, and (b) once taken up, form a duplex with the target ssRNA with a Tm greater than about 50° C.
As will be described below, the ability to be taken up by cells requires that the oligomer backbone be substantially uncharged, and, preferably, that the oligomer structure is recognized as a substrate for active or facilitated transport across the cell membrane. The ability of the oligomer to form a stable duplex with the target RNA will also depend on the oligomer backbone, as well as factors noted above, the length and degree of complementarity of the antisense oligomer with respect to the target, the ratio of G:C to A:T base matches, and the positions of any mismatched bases. The ability of the antisense oligomer to resist cellular nucleases promotes survival and ultimate delivery of the agent to the cell cytoplasm.
Below are disclosed methods for testing any given, substantially uncharged backbone for its ability to meet these requirements.
A1. Active or Facilitated Uptake by Cells
The antisense compound may be taken up by host cells by facilitated or active transport across the host cell membrane if administered in free (non-complexed) form, or by an endocytotic mechanism if administered in complexed form.
In the case where the agent is administered in free form, the antisense compound should be substantially uncharged, meaning that a majority of its intersubunit linkages are uncharged at physiological pH. Experiments carried out in support of the invention indicate that a small number of net charges, e.g., 1-2 for a 15- to 20-mer oligomer, can in fact enhance cellular uptake of certain oligomers with substantially uncharged backbones. The charges may be carried on the oligomer itself, e.g., in the backbone linkages, or may be terminal charged-group appendages. Preferably, the number of charged linkages is no more than one charged linkage per four uncharged linkages. More preferably, the number is no more than one charged linkage per ten, or no more than one per twenty, uncharged linkages. In one embodiment, the oligomer is fully uncharged.
An oligomer may also contain both negatively and positively charged backbone linkages, as long as opposing charges are present in approximately equal number. Preferably, the oligomer does not include runs of more than 3-5 consecutive subunits of either charge. For example, the oligomer may have a given number of anionic linkages, e.g. phosphorothioate or N3′→P5′ phosphoramidate linkages, and a comparable number of cationic linkages, such as N,N-diethylenediamine phosphoramidates (Dagle, Littig et al. 2000). The net charge is preferably neutral or at most 1-2 net charges per oligomer.
In addition to being substantially or fully uncharged, the antisense agent is preferably a substrate for a membrane transporter system (i.e. a membrane protein or proteins) capable of facilitating transport or actively transporting the oligomer across the cell membrane. This feature may be determined by one of a number of tests for oligomer interaction or cell uptake, as follows.
A first test assesses binding at cell surface receptors, by examining the ability of an oligomer compound to displace or be displaced by a selected charged oligomer, e.g., a phosphorothioate oligomer, on a cell surface. The cells are incubated with a given quantity of test oligomer, which is typically fluorescently labeled, at a final oligomer concentration of between about 10-300 nM. Shortly thereafter, e.g., 10-30 minutes (before significant internalization of the test oligomer can occur), the displacing compound is added, in incrementally increasing concentrations. If the test compound is able to bind to a cell surface receptor, the displacing compound will be observed to displace the test compound. If the displacing compound is shown to produce 50% displacement at a concentration of 10× the test compound concentration or less, the test compound is considered to bind at the same recognition site for the cell transport system as the displacing compound.
A second test measures cell transport, by examining the ability of the test compound to transport a labeled reporter, e.g., a fluorescence reporter, into cells. The cells are incubated in the presence of labeled test compound, added at a final concentration between about 10-300 nM. After incubation for 30-120 minutes, the cells are examined, e.g., by microscopy, for intracellular label. The presence of significant intracellular label is evidence that the test compound is transported by facilitated or active transport.
The antisense compound may also be administered in complexed form, where the complexing agent is typically a polymer, e.g., a cationic lipid, polypeptide, or non-biological cationic polymer, having an opposite charge to any net charge on the antisense compound. Methods of forming complexes, including bilayer complexes, between anionic oligonucleotides and cationic lipid or other polymer components, are well known. For example, the liposomal composition Lipofectin® (Felgner, Gadek et al. 1987), containing the cationic lipid DOTMA (N-[1-(2,3-dioleyloxy)propyl]-N,N,N-trimethylammonium chloride) and the neutral phospholipid DOPE (dioleyl phosphatidyl ethanolamine), is widely used. After administration, the complex is taken up by cells through an endocytotic mechanism, typically involving particle encapsulation in endosomal bodies.
The antisense compound may also be administered in conjugated form with an arginine-rich peptide linked to the 5′ or 3′ end of the antisense oligomer. The peptide is typically 8-16 amino acids and consists of a mixture of arginine, and other amino acids including phenyalanine and cysteine. Exposure of cells to the peptide conjugated oligomer results in enhanced intracellular uptake and delivery to the RNA target.
Alternatively, and according to another aspect of the invention, the requisite properties of oligomers with any given backbone can be confirmed by a simple in vivo test, in which a labeled compound is administered to an animal, and a body fluid sample, taken from the animal several hours after the oligomer is administered, assayed for the presence of heteroduplex with target RNA. This method is detailed in subsection D below.
A2. Substantial Resistance to RNaseH
Two general mechanisms have been proposed to account for inhibition of expression by antisense oligonucleotides (Agrawal, Mayrand et al. 1990; Bonham, Brown et al. 1995; Boudvillain, Guerin et al. 1997). In the first, a heteroduplex formed between the oligonucleotide and the viral RNA acts as a substrate for RNaseH, leading to cleavage of the viral RNA. Oligonucleotides belonging, or proposed to belong, to this class include phosphorothioates, phosphotriesters, and phosphodiesters (unmodified “natural” oligonucleotides). Such compounds expose the viral RNA in an oligomer:RNA duplex structure to hydrolysis by RNaseH, and therefore loss of function.
A second class of oligonucleotide analogs, termed “steric blockers” or, alternatively, “RNaseH inactive” or “RNaseH resistant”, have not been observed to act as a substrate for RNaseH, and are believed to act by sterically blocking target RNA nucleocytoplasmic transport, splicing, translation, or replication. This class includes methylphosphonates (Toulme, Tinevez et al. 1996), morpholino oligonucleotides, peptide nucleic acids (PNA's), certain 2′-O-allyl or 2′-O-alkyl modified oligonucleotides (Bonham, Brown et al. 1995), and N3′→P5′ phosphoramidates (Ding, Grayaznov et al. 1996; Gee, Robbins et al. 1998).
A test oligomer can be assayed for its RNaseH resistance by forming an RNA:oligomer duplex with the test compound, then incubating the duplex with RNaseH under a standard assay conditions, as described in Stein et al (Stein, Foster et al. 1997). After exposure to RNaseH, the presence or absence of intact duplex can be monitored by gel electrophoresis or mass spectrometry.
A3. In Vivo Uptake
In accordance with another aspect of the invention, there is provided a simple, rapid test for confirming that a given antisense oligomer type provides the required characteristics noted above, namely, high Tm, ability to be actively taken up by the host cells, and substantial resistance to RNaseH. This method is based on the discovery that a properly designed antisense compound will form a stable heteroduplex with the complementary portion of the viral RNA target when administered to a mammalian subject, and the heteroduplex subsequently appears in the urine (or other body fluid). Details of this method are also given in co-owned U.S. patent applications, Ser. No.09/736,920, entitled “Non-Invasive Method for Detecting Target RNA” (Non-Invasive Method), the disclosure of which is incorporated herein by reference.
Briefly, a test oligomer containing a backbone to be evaluated, having a base sequence targeted against a known RNA, is injected into an animal, e.g., a mammalian subject. The antisense oligomer may be directed against any intracellular RNA, including a host RNA or the RNA of an infecting virus. Several hours (typicaly 8-72) after administration, the urine is assayed for the presence of the antisense-RNA heteroduplex. If heteroduplex is detected, the backbone is suitable for use in the antisense oligomers of the present invention.
The test oligomer may be labeled, e.g. by a fluorescent or a radioactive tag, to facilitate subsequent analyses, if it is appropriate for the mammalian subject. The assay can be in any suitable solid-phase or fluid format. Generally, a solid-phase assay involves first binding the heteroduplex analyte to a solid-phase support, e.g., particles or a polymer or test-strip substrate, and detecting the presence/amount of heteroduplex bound. In a fluid-phase assay, the analyte sample is typically pretreated to remove interfering sample components. If the oligomer is labeled, the presence of the heteroduplex is confirmed by detecting the label tags. For non-labeled compounds, the heteroduplex may be detected by immunoassay if in solid phase format or by mass spectroscopy or other known methods if in solution or suspension format.
When the antisense oligomer is complementary to a virus-specific region of the viral genome (such as the region encompassing the Nidovirus leader TRS), the method can be used to detect the presence of a given ssRNA virus. The method can also be use to monitor the reduction in the amount of virus during a treatment method.
B. Exemplary Oligomer Backbones
Examples of nonionic linkages that may be used in oligonucleotide analogs are shown in
Peptide nucleic acids (PNAs) (
A preferred oligomer structure employs morpholino-based subunits bearing base-pairing moieties, joined by uncharged linkages, as described above. Especially preferred is a substantially uncharged phosphorodiamidate-linked morpholino oligomer, such as illustrated in
Important properties of the morpholino-based subunits include: the ability to be linked in a oligomeric form by stable, uncharged backbone linkages; the ability to support a nucleotide base (e.g. adenine, cytosine, guanine or uracil) such that the polymer formed can hybridize with a complementary-base target nucleic acid, including target RNA, with high Tm, even with oligomers as short as 10-14 bases; the ability of the oligomer to be actively transported into mammalian cells; and the ability of the oligomer:RNA heteroduplex to resist RNAse degradation.
Exemplary backbone structures for antisense oligonucleotides of the invention include the β-morpholino subunit types shown in
The linkages shown in
As noted above, the substantially uncharged oligomer may advantageously include a limited number of charged linkages, e.g. up to about 1 per every 5 uncharged linkages, more preferably up to about 1 per every 10 uncharged linkages. Therefore a small number of charged linkages, e.g. charged phosphoramidate or phosphorothioate, may also be incorporated into the oligomers.
The antisense compounds can be prepared by stepwise solid-phase synthesis, employing methods detailed in the references cited above. In some cases, it may be desirable to add additional chemical moieties to the antisense compound, e.g. to enhance pharmacokinetics or to facilitate capture or detection of the compound. Such a moiety may be covalently attached, typically to a terminus of the oligomer, according to standard synthetic methods. For example, addition of a polyethyleneglycol moiety or other hydrophilic polymer, e.g., one having 10-100 monomeric subunits, may be useful in enhancing solubility. One or more charged groups, e.g., anionic charged groups such as an organic acid, may enhance cell uptake. A reporter moiety, such as fluorescein or a radiolabeled group, may be attached for purposes of detection. Alternatively, the reporter label attached to the oligomer may be a ligand, such as an antigen or biotin, capable of binding a labeled antibody or streptavidin. In selecting a moiety for attachment or modification of an antisense oligomer, it is generally of course desirable to select chemical compounds of groups that are biocompatible and likely to be tolerated by a subject without undesirable side effects.
V. Inhibition of Viral Replication
The antisense compounds detailed above are useful in inhibiting replication of Nidoviruses in animal cells, including mammalian cells, e.g., human cells, and avian cells. In one embodiment, such inhibition is effective in treating infection of a host animal by these viruses. Accordingly, the method comprises, in one embodiment, contacting a cell infected with the virus with an antisense agent effective to inhibit the replication of the specific virus. In this embodiment, the antisense agent is administered to a mammalian subject, e.g., human or domestic animal, infected with a given virus, in a suitable pharmaceutical carrier. It is contemplated that the antisense oligonucleotide arrests the growth of the RNA virus in the host. The RNA virus may be decreased in number or eliminated with little or no detrimental effect on the normal growth or development of the host.
A. Identification of the Infective Agent
The specific virus causing the infection can be determined by methods known in the art, e.g. serological or cultural methods, or by methods employing the antisense oligomers of the present invention.
Serological identification employs a viral sample or culture isolated from a biological specimen, e.g., stool, urine, cerebrospinal fluid, blood, etc., of the subject. Immunoassay for the detection of virus is generally carried out by methods routinely employed by those of skill in the art, e.g., ELISA or Western blot. In addition, monoclonal antibodies specific to particular viral strains or species are often commercially available.
Culture methods may be used to isolate and identify particular types of virus, by employing techniques including, but not limited to, comparing characteristics such as rates of growth and morphology under various culture conditions.
Another method for identifying the viral infective agent in an infected subject employs one or more antisense oligomers targeting a spectrum of viral species. Sequences targeting any characteristic viral RNA can be used. The desired target sequences are preferably (i) common to broad virus families/genera, and (ii) not found in the infected host, e.g., humans. Characteristic nucleic acid sequences for a large number of infectious viruses are available in public databases, and may serve as the basis for the design of specific oligomers.
For each plurality of oligomers, the following steps are carried out: (a) the oligomer(s) are administered to the subject; (b) at a selected time after said administering, a body fluid sample is obtained from the subject; and (c) the sample is assayed for the presence of a nuclease-resistant heteroduplex comprising the antisense oligomer and a complementary portion of the viral genome. Steps (a)-(c) are carried for at least one such oligomer, or as many as is necessary to identify the virus or family of viruses. Oligomers can be administered and assayed sequentially or, more conveniently, concurrently. The virus is identified based on the presence (or absence) of a heteroduplex comprising the antisense oligomer and a complementary portion of the viral genome of the given known virus or family of viruses.
Preferably, a first group of oligomers, targeting broad families, is utilized first, followed by selected oligomers complementary to specific genera and/or species and/or strains within the broad family/genus thereby identified. This second group of oligomers includes targeting sequences directed to specific genera and/or species and/or strains within a broad family/genus. Several different second oligomer collections, i.e. one for each broad virus family/genus tested in the first stage, are generally provided. Sequences are selected which are (i) specific for the individual genus/species/strains being tested and (ii) not found in humans.
B. Administration of the Antisense Oligomer
Effective delivery of the antisense oligomer to the target nucleic acid is an important aspect of treatment. In accordance with the invention, routes of antisense oligomer delivery include, but are not limited to, various systemic routes, including oral and parenteral routes, e.g., intravenous, subcutaneous, intraperitoneal, and intramuscular, as well as inhalation, transdermal and topical delivery. The appropriate route may be determined by one of skill in the art, as appropriate to the condition of the subject under treatment. For example, an appropriate route for delivery of an antisense oligomer in the treatment of a viral infection of the skin is topical delivery, while delivery of an antisense oligomer for the treatment of a viral respiratory infection is by inhalation. The oligomer may also be delivered directly to the site of viral infection, or to the bloodstream.
The antisense oligomer may be administered in any convenient vehicle which is physiologically acceptable. Such a composition may include any of a variety of standard pharmaceutically accepted carriers employed by those of ordinary skill in the art. Examples include, but are not limited to, saline, phosphate buffered saline (PBS), water, aqueous ethanol, emulsions, such as oil/water emulsions or triglyceride emulsions, tablets and capsules. The choice of suitable physiologically acceptable carrier will vary dependent upon the chosen mode of administration.
In some instances, liposomes may be employed to facilitate uptake of the antisense oligonucleotide into cells. (See, e.g., Williams, S. A., Leukemia 10(12):1980-1989, 1996; Lappalainen et al., Antiviral Res. 23:119,1994; Uhlmann et al., ANTISENSE OLIGONUCLEOTIDES: A NEW THERAPEUTIC PRINCIPLE, Chemical Reviews, Volume 90, No.4, pages 544-584,1990; Gregoriadis, G., Chapter 14, Liposomes, Drug Carriers in Biology and Medicine, pp.287-341, Academic Press, 1979). Hydrogels may also be used as vehicles for antisense oligomer administration, for example, as described in WO 93/01286. The oligonucleotides may also be administered in microspheres or microparticles. (See, e.g., Wu, G. Y. and Wu, C. H., J. Biol. Chem. 262:4429-4432,1987). Alternatively, the use of gas-filled microbubbles complexed with the antisense oligomers can enhance delivery to target tissues, as described in U.S. Pat. No. 6,245,747.
Sustained release compositions may also be used. These may include semipermeable polymeric matrices in the form of shaped articles such as films or microcapsules.
In one aspect of the method, the subject is a human subject, e.g., a patient diagnosed as having a localized or systemic viral infection. The condition of a patient may also dictate prophylactic administration of an antisense oligomer of the invention, e.g. in the case of a patient who (1) is immunocompromised; (2) is a burn victim; (3) has an indwelling catheter; or (4) is about to undergo or has recently undergone surgery. In one preferred embodiment, the oligomer is a phosphorodiamidate morpholino oligomer, contained in a pharmaceutically acceptable carrier, and is delivered orally. In another preferred embodiment, the oligomer is a phosphorodiamidate morpholino oligomer (PMO), contained in a pharmaceutically acceptable carrier, and is delivered intravenously (IV).
In another application of the method, the subject is a livestock animal, e.g., a chicken, cat, pig, cow or goat, etc., and the treatment is either prophylactic or therapeutic. In other applications, the infected animal to be treated may be a zoo or wild animal, e.g., seal, penguin, or hawk, subject to one or more nidovirus infections. The invention also includes a livestock and poultry food composition containing a food grain supplemented with a subtherapeutic amount of an antiviral antisense compound of the type described above. Also contemplated is, in a method of feeding livestock and poultry with a food grain supplemented with subtherapeutic levels of an antiviral, an improvement in which the food grain is supplemented with a subtherapeutic amount of an antiviral oligonucleotide composition as described above.
The antisense compound is generally administered in an amount and manner effective to result in a peak blood concentration of at least 200-400 nM antisense oligomer. Typically, one or more doses of antisense oligomer are administered, generally at regular intervals, for a period of about one to two weeks. Preferred doses for oral administration are from about 1-25 mg oligomer per 70 kg. In some cases, doses of greater than 25 mg oligomer/patient may be necessary. For IV administration, preferred doses are from about 0.5 mg to 10 mg oligomer per 70 kg. The antisense oligomer may-be administered at regular intervals for a short time period, e.g., daily for two weeks or less. However, in some cases the oligomer is administered intermittently over a longer period of time. Administration may be followed by, or concurrent with, administration of an antibiotic or other therapeutic treatment. The treatment regimen may be adjusted (dose, frequency, route, etc.) as indicated, based on the results of immunoassays, other biochemical tests and physiological examination of the subject under treatment.
C. Monitoring of Treatment
An effective in vivo treatment regimen using the antisense oligonucleotides of the invention may vary according to the duration, dose, frequency and route of administration, as well as the condition of the subject under treatment (i.e., prophylactic administration versus administration in response to localized or systemic infection). Accordingly, such in vivo therapy will often require monitoring by tests appropriate to the particular type of viral infection under treatment, and corresponding adjustments in the dose or treatment regimen, in order to achieve an optimal therapeutic outcome. Treatment may be monitored, e.g., by general indicators of infection, such as complete blood count (CBC), nucleic acid detection methods, immunodiagnostic tests, viral culture, or detection of heteroduplex.
The efficacy of an in vivo administered antisense oligomer of the invention in inhibiting or eliminating the growth of one or more types of RNA virus may be determined from biological samples (tissue, blood, urine etc.) taken from a subject prior to, during and subsequent to administration of the antisense oligomer. Assays of such samples include (1) monitoring the presence or absence of heteroduplex formation with target and non-target sequences, using procedures known to those skilled in the art, e.g., an electrophoretic gel mobility assay; (2) monitoring the amount of viral protein production, as determined by standard techniques such as ELISA or Western blotting, or (3) measuring the effect on viral titer, e.g. by the method of Spearman-Karber. (See, for example, Pari, G. S. et al., Antimicrob. Agents and Chemotherapy 39(5):1157-1161, 1995; Anderson, K. P. et al., Antimicrob. Agents and Chemotherapy 40(9):2004-2011, 1996, Cottral, G. E. (ed) in: Manual of Standard Methods for Veterinary Microbiology, pp.60-93,1978).
A preferred method of monitoring the efficacy of the antisense oligomer treatment is by detection of the antisense-RNA heteroduplex. At selected time(s) after antisense oligomer administration, a body fluid is collected for detecting the presence and/or measuring the level of heteroduplex species in the sample. Typically, the body fluid sample is collected 3-24 hours after administration, preferably about 6-24 hours after administering. As indicated above, the body fluid sample may be urine, saliva, plasma, blood, spinal fluid, or other liquid sample of biological origin, and may include cells or cell fragments suspended therein, or the liquid medium and its solutes. The amount of sample collected is typically in the 0.1 to 10 ml range, preferably about 1 ml or less.
The sample may be treated to remove unwanted components and/or to treat the heteroduplex species in the sample to remove unwanted ssRNA overhang regions, e.g. by treatment with RNase. It is, of course, particularly important to remove overhang where heteroduplex detection relies on size separation, e.g., electrophoresis of mass spectroscopy.
A variety of methods are available for removing unwanted components from the sample. For example, since the heteroduplex has a net negative charge, electrophoretic or ion exchange techniques can be used to separate the heteroduplex from neutral or positively charged material. The sample may also be contacted with a solid support having a surface-bound antibody or other agent specifically able to bind the heteroduplex. After washing the support to remove unbound material, the heteroduplex can be released in substantially purified form for further analysis, e.g., by electrophoresis, mass spectroscopy or immunoassay.
Material and Methods
Production of PMO and Peptide Conjugated PMOs
Phosphorodiamidate morpholino oligomers (PMOs) were synthesized at AVI BioPharma (Corvallis, Oreg.) as previously describe (Summerton and Weller 1997). Purity of full length oligomers was >95% as determined by reverse-phase high-pressure liquid chromatography (HPLC) and MALDI TOF mass spectroscopy. To facilitate cellular uptake by in vitro cultured cells, peptide conjugated forms of the PMOs were produced by attaching the carboxy terminal cysteine of the peptide to the 5′ end of the PMO through a cross-linker N-[□-maleimidobutyryloxy]succinimide ester (GMBS) (Moulton and Moulton 2003). The peptide used in this study is designated as P003 (R9F2C, SEQ ID NO:47). The lyophilized PMOs or peptide-conjugated PMOs were dissolved in sterile H2O prior to use in cell cultures.
The capability of an antiviral drug to reduce the production of viable virus is a classic measure of antiviral drug activity. The reduction of SARS virus titer produced from SARS-infected Vero-E6 cells cultured in the presence of anti-leader TRS PMO (SEQ ID NOS:26 and 27) was measured and the results shown in
Vero-E6 cells were cultured in DMEM with 10% fetal bovine serum. Vero-E6 cells were plated at approximately 75% confluence in replicate 25 cm2 culture flasks. Cells were rinsed and incubated in 1 ml of complete VP-SFM (virus production serum-free medium, Invitrogen) containing the specified concentration of antisense PMO-P003 conjugate (SEQ ID NOS: 26 or 27) or a PMO-P003 conjugate with an irrelevant sequence (DSscr) for 12-16h (overnight). Cells were transferred to the BSL-3 containment facility at this point and inoculated with SARS-CoV at a multiplicity of approximately 0.1 PFU/cell by adding virus directly to the treatment medium for 1 h at 37 C and in the presence of 5% CO2. Other multiplicities were tested in some experiments and drug effects were not found to differ. After 1 h adsorbtion, 4 ml of VP-SFM was added and cells were incubated for 24 h. Virus-containing supernatants were collected and stored at −80 C until titration. Titration was by standard Vero-E6 plaque assay. Wells containing approximately 75% confluent Vero-E6 cells were inoculated with serial dilutions of virus, incubated 1 h at 37 C in the presence of 5% CO2 and then overlaid with 0.7% agarose in 1× DMEM. Cells were incubated 72 h, fixed by immersion of the plate in 10% formalin saline for 24 h, surface decontaminated with 95% ethanol and removed from the BSL-3 facility. Plaques were visualized with 0.1% crystal violet and counted. Virus titer is calculated and presented in
The same method was used to determine the antiviral activity of a P003-PMO conjugate (SEQ ID NO:47 conjugated to SEQ ID NO:29) targeted to the TRS leader sequence of MHV. A reduced viral titer was observed as shown in
As a separate measure of the antiviral activity of antisense PMO drugs, the anti-leader TRS PMOs were used to measure the reduction of viral replication in a plaque size assay. As viral replication is inhibited a corresponding reduction in the spread of cytopathic effects is observed as a reduction in plaque size. Furthermore, since virus entry and spread are separable phenomena with different criteria, and since some reports indicate that the antisense PMO drugs may inhibit initial virus entry, the plaque size reduction assay is performed. This assay also tests the non-toxicity of drug over longer treatment periods.
As described above in Example 1, 75% confluent Vero-E6 cells were prepared in plates but not pretreated. Cells were transported to the BSL-3 facility, inoculated with serial dilutions of SARS virus calculated to produce 1, 10 and 100 plaques per plate. The same serial dilution stocks were used for all control and test plate inoculations. After 1 h adsorbtion of inoculum, cells were overlaid with 0.7% agarose in 0.25× PBS, 0.75× VP-SFM to make an isotonic nutrient overlay. Each overlay was made separately with PMO-P003 conjugate (SEQ ID NOS: 26 and 27) added to the molten agaroseNP-SFM preparation immediately prior to overlay. Overlay volume is 2 ml and drug is added to make this volume up to the desired concentration. Cells are incubated at 37 C in the presence of 5% CO2 for 72 h, then fixed, decontaminated and stained as described in Example 1. Plaque diameter was measured for all visible plaques to the nearest 0.5 mm using a ruler. Where fewer pinprick plaques than expected are present at effective concentrations of drug, zero-diameter plaques are recorded to make up the expected titer, based on untreated controls. This is valid since virus binding and entry have been completed prior to differentiation of plates by addition of treatment-overlay. Plaque size was plotted (mean ±SEM) for approximately equal numbers of plaques from replicate wells as shown in
This assay is a byproduct of the virus titer reduction assay. The observation of cytopathic effects (CPE) is a visual measure of antiviral drug activity. Vero-E6 cells were pretreated, inoculated with SARS virus and cultured as above in the presence of anti-leader TRS PMOs (SEQ ID NOS: 26 & 27). After 24 h, the medium was replaced by fresh complete VP-SFM and cells were incubated a further 24 h at 37 C in the presence of 5% CO2. 48 h after inoculation, the cells were fixed, decontaminated and stained with crystal violet as described in Example 1. CPE is visualized by phase contrast microscopy and recorded with a digital camera as shown in
Equine arteritis virus (EAV) is an enveloped plus-strand RNA virus of the family Arteriviridae (order Nidovirales) that causes respiratory and reproductive disease in equids. EAV is the prototype virus for the Arteriviridae family and has been studied extensively at the molecular level (Ziebuhr, Snijder et al. 2000; Pasternak, van den Born et al. 2001; Pasternak, van den Born et al. 2003; Balasuriya, Hedges et al. 2004; Pasternak, Spaan et al. 2004; VAN DEN BORN, GULTYAEV et al. 2004). An anti-leader TRS PMO (SEQ ID NO:46) was used to treat EAV-infected cell cultures and antiviral activity was measured using immunofluorescence as shown in
Vero E6 cells were treated with R9F2C-conjugated PMO (SEQ ID NO:47 conjugated to SEQ ID NO:46) for six hours in culture medium lacking fetal calf serum. After PMO pretreatment, cells were inoculated with EAV at an M.O.I. of 0.5 for one hour. Medium containing 8% serum and no PMO was then added back and the cultures incubated at 37° C. for 24 hours. An immunofluorescence assay (IFA) using two different EAV-specific antibody-fluorescent dye combinations was performed on the cells and the photomicrographs are shown in
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|U.S. Classification||514/44.00A, 536/23.1, 514/81, 544/81|
|International Classification||C07H21/02, A61K48/00, C07F9/6533, C07K14/165, C12N15/113|
|Cooperative Classification||C07H21/02, C12N2310/3233, C12N15/1131, C12N2310/11, C07K14/005, C12N2770/20022, C12N2310/3513|
|European Classification||C07K14/005, C12N15/113A|
|Apr 11, 2005||AS||Assignment|
Owner name: AVI BIOPHARMA, INC., OREGON
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Effective date: 20050405
|Jan 23, 2006||AS||Assignment|
Owner name: SCRIPPS RESEARCH INSTITUTE, THE, CALIFORNIA
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:NEUMAN, BENJAMIN;BUCHMEIER, MICHAEL;REEL/FRAME:017483/0227
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Owner name: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF
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