Assays for the detection of anti-TNF drugs and autoantibodies
View Patent ↗The present invention provides assays for detecting and measuring the presence or level of anti-TNFα drug therapeutics and autoantibodies in a sample. The present invention is useful for optimizing therapy and monitoring patients receiving anti-TNFα drug therapeutics to detect the presence or level of autoantibodies (e.g., HACA and/or HAHA) against the drug.
1. A method for determining the presence or level of an anti-TNFα drug in a sample, the method comprising:
(a) contacting a labeled TNFα with a sample having an anti-TNFα drug to form a labeled complex with the anti-TNFα drug;
(b) subjecting the labeled complex to size exclusion chromatography to separate the labeled complex from free labeled TNFα and to detect an amount of the labeled complex and an amount of the free labeled TNFα; and
(c) comparing the amount of the labeled complex and the amount of the free labeled TNFα detected in step (b) to a standard curve of known amounts of the anti-TNFα drug, thereby determining the presence or level of the anti-TNFα drug.
2. The method of claim 1 , wherein the standard curve is generated by incubating the labeled TNFα with known amounts of the anti-TNFα drug.
3. The method of claim 1 , wherein the sample is serum.
4. The method of claim 1 , wherein the anti-TNFα drug is a member selected from the group consisting of REMICADE™ (infliximab), ENBREL™ (etanercept), HUMIRA™ (adalimumab), CIMZIA® (certolizumab pegol), and combinations thereof.
5. The method of claim 1 , wherein the size exclusion chromatography is size exclusion-high performance liquid chromatography (SE-HPLC).
6. The method of claim 1 , wherein the labeled TNFα is a fluorophore-labeled TNFα.
7. The method of claim 6 , wherein the fluorophore is an Alexa Fluor® dye.
8. The method of claim 1 , wherein the labeled complex is eluted first, followed by the free labeled TNFα.
9. The method of claim 1 , wherein the sample is obtained from a subject receiving therapy with the anti-TNFα drug.
10. A method for determining the presence or level of an autoantibody to an anti-TNFα drug in a sample, the method comprising:
(a) contacting a labeled anti-TNFα drug with the sample to form a labeled complex with the autoantibody;
(b) subjecting the labeled complex to size exclusion chromatography to separate the labeled complex from free labeled anti-TNFα drug and to detect an amount of the labeled complex and an amount of the free labeled anti-TNFα drug; and
(c) comparing the amount of the labeled complex and the amount of the free labeled anti-TNFα drug detected in step (b) to a standard curve of known amounts of the autoantibody, thereby determining the presence or level of the autoantibody.
11. The method of claim 10 , wherein the standard curve is generated by incubating the labeled anti-TNFα drug with serum positive for the autoantibody.
12. The method of claim 10 , wherein the sample is serum.
13. The method of claim 10 , wherein the anti-TNFα drug is a member selected from the group consisting of REMICADE™ (infliximab), ENBREL™ (etanercept), HUMIRA™ (adalimumab), CIMZIA® (certolizumab pegol), and combinations thereof.
14. The method of claim 10 , wherein the autoantibody is a member selected from the group consisting of a human anti-mouse antibody (HAMA), a human anti-chimeric antibody (HACA), a human anti-humanized antibody (HAHA), and combinations thereof.
15. The method of claim 10 , wherein the size exclusion chromatography is size exclusion-high performance liquid chromatography (SE-HPLC).
16. The method of claim 10 , wherein the labeled anti-TNFα drug is a fluorophore-labeled anti-TNFα drug.
17. The method of claim 16 , wherein the fluorophore is an Alexa Fluor® dye.
18. The method of claim 10 , wherein the labeled complex is eluted first, followed by the free labeled anti-TNFα drug.
19. The method of claim 10 , wherein the sample is obtained from a subject receiving therapy with the anti-TNFα drug.
20. The method of claim 10 , wherein a ratio of the free labeled anti-TNFα drug to an internal control is determined and used to extrapolate the level of the autoantibody from the standard curve.