Non-HLA antibodies in solid organ transplantation: recent concepts and clinical relevance

Curr Opin Organ Transplant. 2013 Aug;18(4):430-5. doi: 10.1097/MOT.0b013e3283636e55.

Abstract

Purpose of review: Humoral responses beyond major histocompatibility antigens continue to receive the attention of the transplantation community. We report on clinical studies testing clinical relevance of non-human leukocyte antigen (HLA) antigens in solid organ transplantation and provide an update on novel experimental findings. A conceptual framework on the role of graft microenvironment during initiation of non-HLA-related humoral immunity is addressed as well.

Recent findings: Clinical relevance of antibodies targeting angiotensin type 1 receptor (AT1R-Abs) is broadly confirmed in renal and cardiac transplantation, where in addition antibodies against endothelin type A receptor (ETAR-Abs) were found. Obliterative lesions in lung allografts occur more commonly in the presence of antibodies directed against K-α 1 tubulin and collagen-V. Anti-perlecan antibodies are newly identified as accelerators of obliterative vascular lesions. Changes in the intragraft microenvironment, ischemia and alloimmunity seem to represent important permissive factors for non-HLA antibody responses.

Summary: Confirmed clinical relevance of non-HLA humoral responses in solid organ transplantation emphasizes the need for revision of classical diagnostic approaches based solely on detection of HLA-donor-specific antibodies (DSA). A better understanding of intersections of HLA- and non-HLA-related mechanisms and identification of common effector mechanisms would represent an important step towards targeted therapies.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Autoantibodies / blood*
  • Collagen Type V / immunology*
  • HLA Antigens / immunology
  • Heparan Sulfate Proteoglycans / immunology*
  • Humans
  • Immunity, Humoral / physiology
  • Organ Transplantation*
  • Receptor, Angiotensin, Type 1 / immunology*
  • Receptor, Endothelin A / immunology*
  • Tubulin / immunology*

Substances

  • Autoantibodies
  • Collagen Type V
  • HLA Antigens
  • Heparan Sulfate Proteoglycans
  • Receptor, Angiotensin, Type 1
  • Receptor, Endothelin A
  • Tubulin
  • perlecan