|Publication number||US20070184504 A1|
|Application number||US 11/656,357|
|Publication date||Aug 9, 2007|
|Filing date||Jan 22, 2007|
|Priority date||Mar 1, 2002|
|Also published as||CA2476979A1, CN1639572A, EP1478923A2, EP1478923A4, US7166439, US20030166031, WO2003074549A2, WO2003074549A3|
|Publication number||11656357, 656357, US 2007/0184504 A1, US 2007/184504 A1, US 20070184504 A1, US 20070184504A1, US 2007184504 A1, US 2007184504A1, US-A1-20070184504, US-A1-2007184504, US2007/0184504A1, US2007/184504A1, US20070184504 A1, US20070184504A1, US2007184504 A1, US2007184504A1|
|Inventors||Aaron Vinik, David Taylor-Fishwick|
|Original Assignee||Vinik Aaron I, Taylor-Fishwick David A|
|Export Citation||BiBTeX, EndNote, RefMan|
|Referenced by (6), Classifications (12)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This application is a Divisional Application of parent application Ser. No. 10/376,046, filed on Feb. 27, 2003, which claims the benefit of provisional application Ser. No. 60/361,040 filed on Mar. 1, 2002.
The invention relates to the field of assays for antibodies. Specifically, the invention relates to antibodies raised in mammals against administered therapeutic agents.
Pancreatic islets of Langerhans are the only organ of insulin production in the body. However, they have a limited capacity for regeneration. This limited regeneration capacity predisposes mammals to develop diabetes mellitus. Islet neogenesis associated protein (INGAP) plays a role in stimulation of islet neogenesis, in particular, in beta cell regeneration from ductal cells. INGAP104-118 peptide (IGLHDPSHGTLPNGS, SEQ ID NO: 1), a 15-amino acid peptide comprising amino acids 104-118 of the INGAP protein, is biologically active and is capable of inducing islet cell regeneration in an animal model. Pharmaceutical compositions containing a mammalian INGAP104-118 peptide can be used for treatment of endocrine pancreatic insufficiency which may result from diabetes mellitus.
Antibodies to INGAP104-118 peptide may be generated in patients following repeated dosing of INGAP104-118 peptide or may be generated as autoantibodies to the endogenous protein, which may mitigate the action of INGAP or serve as a diagnostic marker for diabetes. Thus, there is a need in the art for a convenient assay for detecting antibodies that may be raised in a subject following treatment with INGAP104-118 peptide.
One embodiment of the invention is a method for detecting antibodies to INGAP104-118 peptide in a test sample. This method comprises contacting a test sample which comprises serum of a mammal with INGAP104-118 peptide bound to a solid support. The contacting is done under conditions sufficient for binding an anti-INGAP104-118 antibody to the INGAP104-118 peptide. The solid support is contacted with a detection antibody which specifically binds antibody molecules of all isotypes of the mammal. The detection antibody bound to the solid support is determined. Detection antibody bound to the solid support indicates that the test sample contains antibodies to INGAP104-118 peptide.
A second embodiment of the invention is a method for detecting antibodies to INGAP104-118 peptide in a test sample and determining the isotype of said antibodies. This method comprises contacting a test sample which comprises serum of a mammal with INGAP104-118 bound to a solid support. The contacting is done under conditions sufficient for binding an anti-INGAP104-118 antibody to the INGAP104-118 peptide. The solid support is contacted with an isotype-specific antibody which specifically binds antibody molecules of one isotype of the mammal. The isotype specific antibody bound to the solid support is determined. Detection antibody bound to the solid support indicates that the test sample contains antibodies to INGAP104-118 peptide and that the antibodies to the INGAP104-118 peptide are of the one isotype.
A further embodiment of the invention is a kit for detecting an anti-INGAP104-118 antibody in the serum of a mammal. The kit comprises an INGAP104-118 peptide and a detection antibody.
These and other embodiments of the invention provide the art with tools and methods for detecting antibodies that bind to INGAP104-118 peptide which are useful for monitoring subjects during treatment with INGAP104-118 peptide and identifying subjects with INGAP autoantibodies.
It is a discovery of the present invention that anti-INGAP antibodies generated in vivo can be sensitively and specifically detected in a solid phase assay. Anti-INGAP104-118 antibodies can be detected without interference by the components of mammalian serum. Normal human serum does not contain factors that result in false positive signals, nor does it inhibit the interaction of anti-INGAP104-118 antibodies with INGAP104-118 peptide.
Assays of anti-INGAP104-118 antibodies in a sample from a mammal are useful to monitor generation of neutralizing antibodies during the therapeutic administration of INGAP104-118 peptide. Neutralizing antibodies may be endogenous autoantibodies or antibodies generated in subjects following single or repeated dosing with INGAP104-118 peptide. Anti-INGAP104-118 antibodies can be specifically detected with sensitivity.
In a solid phase assay, purified INGAP104-118 peptide can be immobilized on a solid support. Solid phase immunoassays are convenient for ease of separating bound from unbound components. Sequential immunoassay steps, including rinsing between steps and the binding of the detection antibody and development of the indicator reaction, can be easily performed without the need for expensive automation and skill.
Any test sample can be used, including but not limited to blood, plasma, or serum. The invention particularly contemplates test samples containing serum. Serum can be obtained from any mammal including, for example, mouse, rat, rabbit, guinea pig, monkey, dog, cat, cow, goat, pig, and human.
Test samples can be assayed at a single concentration of serum or at multiple concentrations which may be obtained by serial dilution of the serum. Diluent serum can be derived from the same species that is the source of the test sample. Other diluents such as buffers and normal saline can also be used. The highest serial dilution at which a signal can be detected can also be used to characterize a test sample. For example, the highest serial dilution at which a signal can be detected for a first mammal can be compared to that of a second mammal to obtain a relative measure of antibody titer in the first and second mammals.
Any immunoreactive form of INGAP104-118, INGAP or a derivative thereof can be used. Native, synthetic, or recombinant forms of the whole INGAP peptide, or related proteins which contain, or are modified to contain the INGAP104-118 sequence or portions immunoreactive with an antibody against INGAP104-118 peptide may be used. Thus, portions of INGAP104-118 peptide or peptides containing such portions and other residues or moieties can be used. Derivatives include, but are not limited to, modification the peptide's C-terminus, N-terminus, and/or amino acid side chains. Examples of C-terminal carboxylate modifications include esterification (e.g., benzyl, methyl or ethyl ester) and amidation. Examples of N-terminal modifications include acetylation and alkoxycarbonylation. Amino acid side chain modifications include methylation, benzylation, t-butylation, tosylation, alkoxycarbonylation, and the like.
INGAP104-118 peptide, INGAP or a derivative thereof can be produced by any method known in the art. These methods include, but are not limited to inducing mammalian pancreatic cells to express INGAP protein by means of cellophane-wrapping (Rosenberg, L., Brown, R. A. and Duguid, W. P. (1982). Surg. Forum 33, 227-230). Standard recombinant techniques in prokaryotic or eukaryotic host cells can also be used to make full length or portions of INGAP or INGAP104-118 peptide. Suitable host cells include bacteria, yeast, insect, or mammalian cells. Any expression vectors known in the art can be used. Enzymes can be used to generate less than full-length proteins by enzymatic proteolysis of full-length or partial proteins. Synthetic chemistry methods, such as solid-phase peptide synthesis, can be used to synthesize the proteins and polypeptides. The polypeptides can be synthesized directly on the solid support used for the immunoassay of the invention.
INGAP104-118 peptide, INGAP protein, or portions thereof may be purified by means of any technique known in the art of protein purification. Exemplary techniques include ion-exchange chromatography, hydrophobic interaction chromatography, and immunoaffinity methods.
INGAP104-118 peptide is bound to the solid support. It can be adsorbed or chemically coupled to a solid phase support. Any means known in the art for immobilizing a protein or peptide to a solid support can be used. INGAP104-118 peptide can be either covalently or non-covalently bound to the solid phase support by techniques such as covalent bonding via an amide or ester linkage or adsorption. It can be bound using binding pairs such as biotin and avidin or antibody and antigen. After INGAP104-118 peptide is affixed to the solid phase, the solid phase support can be incubated with a blocking solution (containing a blocking protein such as bovine serum albumin) to reduce non-specific adsorption of antibodies in a test sample to the support surface.
Various solid phase supports can be used, including but not limited to glass, polystyrene, polypropylene, nitrocellulose, dextran or other materials. Suitable forms of the solid phase supports include beads, microparticles, tubes, fabrics or plates formed from or coated with these materials. In a preferred embodiment the solid support comprises microtiter wells, such as a 96-well microtiter plate.
A detection antibody is used to assess anti-INGAP104-118 antibody bound to the solid phase support. The detection antibody may be labeled. A label can be any composition which is detectable. Any analytical means known in the art can be used for determining or detecting the detection antibody. These means include the use of spectroscopy, chemistry, photochemistry, biochemistry, immunochemistry, or optics. The label can be, for example, an enzyme (e.g., horseradish peroxidase, alkaline phosphatase, beta-galactosidase, and others commonly used in an ELISA), a radiolabel (e.g., 3H, 125I, 35S, 14C, or 32P), a chemiluminescent compound (e.g. luciferin, and 2,3-dihydrophthalazinediones, luminol, etc.), a fluorescent dye (e.g., fluorescein isothiocyanate, Texas red, rhodamine, etc.), or any other dye known in the art.
The label may be coupled directly or indirectly (e.g., via binding pairs such as biotin and avidin) to the detection antibody according to methods well known in the art. As indicated above, a wide variety of labels may be used. The choice of label may depend on sensitivity required, ease of conjugation with the compound, stability requirements, available instrumentation, or disposal provisions. For a review of various labeling or signal producing systems which may be used, see U.S. Pat. No. 4,391,904.
Detection antibodies can be detected or determined by any suitable method known in the art. A label on an antibody can be detected by a gamma counter if the label is a radioactive gamma emitter, or by a fluorimeter, if the label is a fluorescent material. In the case of an enzyme, the label can be detected calorimetrically employing a substrate for the enzyme. In a preferred embodiment, the detection antibody is detected using alkaline phosphatase-conjugated, species-specific immunoglobulin. Any substrate of alkaline phosphatase can be used. For example, p-nitrophenylphosphate (pNPP) can be the substrate and the reaction product, p-nitrophenol, can be detected optically.
Results of the assay may be qualitative or quantitative. The amount of label associated with the support can be compared with positive and negative controls in order to determine the presence of anti-INGAP104-118 antibodies. The controls are typically run concomitantly with the sample to be tested. A positive control can be a serum containing antibodies that are immunoreactive with the INGAP104-118 peptide. A negative control can be a serum which does not contain antibodies that are immunoreactive with the INGAP104-118 peptide. For quantitation, a standard curve using known quantities of anti-INGAP104-118 antibody can be generated and/or used.
Antibodies for use as positive controls may be produced using all, or fragments of, the amino acid sequence of an INGAP protein. “Antibody” as used herein includes intact immunoglobulin molecules, as well as fragments thereof, such as Fab, F(ab′)2, and Fv, which are capable of binding an epitope of INGAP104-118 peptide. Any type of antibody known in the art can be generated to bind specifically to an epitope of an INGAP104-118 peptide. Monoclonal or polyclonal antibodies can be made as is well known in the art.
Any technique for purifying anti-INGAP104-118 antibodies as are available in the art can be used. For example, antibodies can be purified by known methods such as affinity separation using protein A, high pressure liquid chromatography on reverse phase alkylated silica gel, or gel filtration. Antibodies can also be passed over a solid phase to which INGAP104-118 peptide is bound. The anti-INGAP antibodies will bind to the INGAP104-118 peptide bound to the solid support and the contaminants can be washed away. The bound antibodies can be eluted, for example, with a buffer having a high salt concentration.
The particular parameters employed in the assay of the present invention can vary widely depending on various factors such as the concentration of antibody in the sample, the nature of the sample, the type of immunoassay employed and the like. Optimal conditions can be readily established by those of ordinary skill in the art. Typical assay conditions include a temperature range of about 4° C. to about 45° C. and a pH value range of about 5 to 9. Incubation times can vary widely depending upon the nature of the assay, and generally range from about 0.1 minute to about 24 hours. A wide variety of buffers, for example TRIS-buffered saline, may be employed, and other reagents such as salt to enhance ionic strength, proteins such as serum albumin, stabilizers, and non-ionic detergents may also be included. Exemplary conditions are given in Example 2.
The isotype of an anti-INGAP104-118 antibody, e.g., IgG, IgD, IgE, IgA, or IgM, can be determined. The biological functions and biochemical characteristics of isotypes differ and the isotype of antibodies present in a test sample can characterize the type of immune response in a subject. Thus, distinguishing the isotypes of immunoglobulin molecules present in a sample can be useful. Any method known in the art to determine antibody isotypes is contemplated. For example, isotype determination can be carried out on a solid support which is bound with INGAP104-118 peptide. The sample to be tested can be contacted with the peptide-bound solid support and a detection antibody can be used. The detection antibody used for this purpose can be isotype-specific. The isotype-specific detection antibody can be labeled and detected as described above. Antibody subisotypes can also be determined by any method known in the art.
Another embodiment of the present invention is a kit for detecting anti-INGAP104-118 antibodies in a mammalian serum. The kit can be useful, inter alia, for monitoring anti-INGAP104-118 antibodies occurring spontaneously or produced during therapy which involves single or repeated dosing of an individual with INGAP104-118. The kit will typically contain in a divided or undivided container an INGAP104-118 peptide which can be used, inter alia, to coat a solid support. Alternatively, the kit can contain a solid support which is already coated with INGAP104-118 peptide. The kit may also contain anti-INGAP104-118 antibodies to serve as a positive control and for use in a standard curve. A detection antibody which is species specific, but isotype-generic can also be included. The detection antibody may be detectably labeled. The kit may also contain isotype-specific detection antibodies for determination of antibody isotype. Instructions, standard curves, and buffers can be optionally included in the kit.
The following examples are merely exemplary and are not intended to limit the scope of the invention.
Specificity of Anti-INGAP104-118 Antibodies
To examine the specificity of the rabbit anti-INGAP104-118 antibody, rabbit anti-INGAP104-118 antibody was incubated in microtiter wells pre-coated with INGAP104-118, bovine serum albumin (BSA), INGAP151-164 (Cterm), or INGAP139-152 (Cseq). All peptide-coated wells had an equivalent concentration of peptide. Anti-INGAP104-118 antibody binding was assessed using an anti-rabbit IgG alkaline phosphatase (AP) conjugate detection antibody. Samples were incubated with pNPP and the optical density (OD) monitored at 405 nm.
Sensitivity of Anti-INGAP104-118 Antibodies
The sensitivity of rabbit anti-INGAP104-118 antibody was determined by incubating rabbit anti-INGAP104-118 antibody with various concentrations of INGAP104-118 peptide in microtiter wells pre-coated with various concentrations of INGAP104-118 peptide. The data is shown in
Normal human serum was found not to affect the anti-INGAP104-118 antibody detection assay. To wells of a microtiter plate pre-coated with INGAP104-118 peptide various concentrations of rabbit anti-INGAP104-118 antibody were added. Anti-INGAP104-118 antibody was serial diluted in buffer containing normal human serum at either 0% (control), 5%, 10%, 15%, 30% or 50%. See
It was also determined that there are no antibodies present in normal human serum that interact with INGAP104-118 peptide. Following the same experimental protocol as described above, normal human serum was screened with AP-conjugated, anti-human immunoglobulin. No detection antibody was detected indicating that no antibodies present the normal human serum were capable of binding to INGAP104-118 peptide. See
Based upon the data, the assay successfully detects INGAP104-118 peptide specific antibodies. Moreover, the assay is functional in the presence of normal human serum. Therefore, this assay is suitable to screen for the presence of anti-INGAP104-118 antibodies in patient sera. The assay is simple and can readily be streamlined to accommodate medium to high throughput screening of samples.
The reagents used in this example are as follows: TBS (0.05 M TRIS, 0.138 M NaCl, 0.0027 KCl, pH 8.0 at 25° C.), TBS-TW (TBS containing 0.05% Tween-20 (polyoxyethylene-borbitan monolaurate)), Blocking Solution for Matrix Dilution Buffer (TBS-TW containing 1% w/v bovine serum albumin), Secondary Antibody Detection for Human Sera (1:5000 dilution of anti-human IGg, AP conjugated (Sigma A-1543) in Blocking solution), Secondary Antibody Detection for Rabbit Antibody (1:5000 dilution of anti-rabbit IGg, AP conjugated (Sigma A-2556) in Blocking solution), Matrix Dilution Buffer (1:25 human serum:blocking solution, v/v), and pNPP Substrate Buffer (one set para-nitrophenyl phosphate tablets (Sigma N-1891) in 5 mL deionized water).
Rabbit anti-INGAP104-118 antibody was supplied by Strelitz Diabetes Institute.
Standard Curve—Standard curve was prepared according to the following table:
250 ng/mL Matrix Calibration Matrix rabbit anti- Dilution Standard Concen- Calibration INGAP104-118 buffer Concentration tration Standard (μL) (μL) (ng/ml) (ng/mL) S-01 500 — 250 6250 S-02 180 120 150 3750 S-03 160 240 100 2500 S-04 80 320 50.0 1250 S-05 30 270 25.0 625 S-06 Using 270 10.0 250 standard -03 30 S-07 Using 270 5.0 125 standard -04 30
Assays were carried out in 96-well microtiter plates. Standards were prepared as indicated in the table shown above, making enough standard to add 100 μL in duplicate to each desired plate well. Desired standard concentrations were made by serial diluting rabbit anti-INGAP104-118 antibody standard with Matrix Dilution Buffer.
A control serum sample was prepared from blank human serum in the same dilution range as the preparative samples. False positive results were not generated due to the concentration of the serum or any proteins in normal human serum that will cross react with the INGAP104-118 peptide.
Plate blanks were prepared by adding 100 μL of the highest concentration standard to wells H1 and H2 on each subsequent plate. These wells were not coated with INGAP104-118 peptide. All reagents should be added to these samples. Wells designated by the plate design served as the blank subtraction value for all wells used in that batch. When plate blanks were not available due to a second batch being analyzed on the same plate, the control blanks were used.
All quality control samples were prepared in duplicate. All unknown samples were prepared in duplicate and 100 μL of each sample was diluted with 2400 μL Matrix Dilution Buffer before microtiter plate analysis.
Microtiter plate analysis was performed as follows: 100 μL of either standard, control blank, quality control sample or unknown sample was added to each plate well. The wells were covered with mylar covers and incubated at room temperature for at least 1 hour at room temperature or overnight at 4° C. The wells were washed by filling each well three times with TBS-TW, making sure to remove all excess liquid between washes. 100 μL of anti-human IgG AP-conjugated antibody was added to serum samples and control serum only. 100 μL of anti-rabbit IgG AP-conjugated antibody was added to calibration standards and quality control standards. These were incubated 1-2 hours at room temperature. Each well was washed once with TBS-TW and then twice with TBS, again making sure to remove all excess liquid between washes. To each well, 100 μL of pNPP substrate buffer was added. Color was allowed to develop for approximately 30 minutes or to the desired color intensity. The target value for the maximum color development was 2.5 OD for the highest calibration standard so the color development was monitored frequently. Multiple plate readings were obtained to monitor color development. Color development was read at ˜30 minutes (development will vary with conditions). Overdevelopment occurs when the high standard is over the linear range of the instrument.
The standard curve was calculated using a point-point fitting based on the OD at 405 nm. All samples where the OD exceeds the highest point of the standard curve were re-prepared at an appropriate dilution. Sample results were calculated against the resulting point-to-point curve. Up to two non-consecutive points may be dropped from the curve based on obvious analytical errors or non-typical color development.
Quality control samples were considered acceptable if they were within 20% of theoretical.
Positive sera were defined as those samples with an OD405 of greater than 0.800 at a dilution of 1:25. Sera comparison between positive patient samples were based on the titer (dilution of sera) required to give a standard signal readout (i.e. 0.800 OD405 units).
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US7989415||Dec 10, 2009||Aug 2, 2011||Curedm Group Holdings, Llc||Peptides, derivatives and analogs thereof, and methods of using same|
|US8211430||Mar 3, 2006||Jul 3, 2012||Curedm Group Holdings, Llc||Methods and pharmaceutical compositions for treating type 1 diabetes mellitus and other conditions|
|US8383578||Jun 24, 2011||Feb 26, 2013||Curedm Group Holdings, Llc||Peptides, derivatives and analogs thereof, and methods of using same|
|US8785400||Nov 21, 2007||Jul 22, 2014||Curedm Group Holdings, Llc||Methods and compositions relating to islet cell neogenesis|
|US8816047||Aug 29, 2008||Aug 26, 2014||Cure DM Group Holdings, LLC||Compositions and methods of using proislet peptides and analogs thereof|
|US8829158||Jan 18, 2013||Sep 9, 2014||Curedm Group Holdings, Llc||Peptides, derivatives and analogs thereof, and methods of using same|
|International Classification||C07K16/18, G01N33/543, C07K14/47, G01N33/68, G01N33/537, G01N33/53|
|Cooperative Classification||G01N2333/474, G01N33/6854, G01N2410/00, G01N2333/4733|