Protein biomarkers for immune assessment and prediction of transplant rejection

US10451636B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10451636-B2
Application numberUS-201515302463-A
CountryUS
Kind codeB2
Filing dateApr 9, 2015
Priority dateApr 9, 2014
Publication dateOct 22, 2019
Grant dateOct 22, 2019

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The invention provides a method for screening for and detection of solid organ graft rejection in a subject that comprises assaying a patient sample of plasma, serum or blood from the subject for a protein marker identified herein. An elevated or reduced amount of marker present in the patient sample compared to a control sample is indicative of rejection, and identifies subjects in need of biopsy or modified treatment. The method can be used to screen for patients in danger of transplant rejection without having to undergo more costly, risky and invasive biopsy procedures.

First claim

Opening claim text (preview).

The invention claimed is: 1. A kit comprising: (a) a solid support coated with polyclonal or monoclonal antibodies, wherein the antibodies comprise antibodies specific to Apolipoprotein A1 (Apo A1), Complement C1 inhibitor (C1-inh), and Alpha-2-macroglobulin (A2M); (b) polyclonal or monoclonal antibody-substrate conjugates, wherein the substrate comprises a chromogenic or fluorescent reagent, and wherein the conjugates are reactive with the antibodies of (a); and (c) Apo A1, C1-inh, and A2M, as antigen standards. 2. The kit of claim 1 , wherein the antibodies of (a) further include antibodies specific to Inter-alpha-trypsin inhibitor heavy chain H4 (ITIH4). 3. The kit of claim 1 , wherein the antibodies of (a) further include antibodies specific to α-1 anti-chymotrypsin (AACT). 4. The kit of claim 1 , wherein the antibodies of (a) further include antibodies specific to AACT and/or ITIH4 and/or Complement C4 Anaphylatoxin (C4A). 5. The kit of claim 1 , wherein the solid support is a microtiter plate or membrane. 6. The kit of claim 1 , wherein the solid support is a bead or particle. 7. The kit of claim 1 , wherein the kit is an ELISA kit. 8. The kit of claim 1 , wherein the solid support is a microbead array. 9. The kit of claim 1 , wherein the antibodies of (a) are specific to 8 or fewer markers, and wherein the antibodies of (a) further comprise antibodies specific to up to five markers selected from the group consisting of: AACT, ITIH4, C4A, Serum Amyloid A (SAA), C-reactive Protein (CRP), Apolipoprotein E (ApoE), Alpha-1-antitrypsin (A1AT), ApoA1 fragment consisting of SEQ ID NO: 5, A1AT fragment consisting of SEQ ID NO: 11, and C4A (SEQ ID NO: 2 or 3). 10. The kit of claim 1 , wherein the antibodies of (a) further comprise antibodies specific to AACT and ITIH4. 11. A method for assaying a combination of markers in a sample of biological fluid obtained from a human subject, the method comprising performing an immunoassay by contacting the sample with the solid support of the kit of claim 1 . 12. The method of claim 11 , wherein the immunoassay is an ELISA. 13. The method of claim 11 , wherein the solid support is a microbead array. 14. The method of claim 11 , wherein the sample is plasma or serum. 15. The method of claim 11 , further comprising contacting the sample with the conjugates of the kit, and assaying the reaction of the conjugates with the sample. 16. The method of claim 15 , further comprising contacting the antigen standards with the solid support and the conjugates, and assaying the relative levels of Apo A1, C1-inh, and A2M in the sample relative to the antigen standards. 17. A method of assaying Apolipoprotein A1 (Apo A1), Complement C1 inhibitor (C1-inh), and Alpha-2-macroglobulin (A2M) in a sample of serum or plasma, the method comprising contacting the sample with the solid support and the conjugates of the kit of claim 1 ; wherein the solid support comprises a microtiter plate, wherein the conjugates comprise alkaline phosphatase, wherein the chromogenic reagent comprises p-nitrophenyl-phosphate; and assaying the reaction of the conjugates with the sample. 18. The method of claim 17 , further comprising assaying ITIH4. 19. The method of claim 17 , further comprising assaying AACT and A1AT.

Assignees

Inventors

Classifications

  • related to diseases not provided for elsewhere · CPC title

  • Immunoglobulins · CPC title

  • Apolipopeptides · CPC title

  • Transplantation related diseases, e.g. graft versus host disease · CPC title

  • Complement proteins, e.g. anaphylatoxin, C3a, C5a · CPC title

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What does patent US10451636B2 cover?
The invention provides a method for screening for and detection of solid organ graft rejection in a subject that comprises assaying a patient sample of plasma, serum or blood from the subject for a protein marker identified herein. An elevated or reduced amount of marker present in the patient sample compared to a control sample is indicative of rejection, and identifies subjects in need of bio…
Who is the assignee on this patent?
Univ California
What technology area does this patent fall under?
Primary CPC classification G01N33/6893. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue Oct 22 2019 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).