Cutting Edge: Allograft Rejection Is Associated with Weak T Cell Responses to Many Different Graft Leukocyte-Derived Peptides

J Immunol. 2018 Jan 15;200(2):477-482. doi: 10.4049/jimmunol.1701434. Epub 2017 Dec 18.

Abstract

Organ transplants are rapidly rejected because T cells in the recipient attack the foreign MHC molecules on the graft. The robustness of the T cell response to histoincompatible tissue is not understood. We found that mice have many small T cell populations with Ag receptors specific for a foreign MHC class II molecule type loaded with peptides from leukocytes from the graft. These T cells proliferated modestly after skin transplantation and underwent relatively weak functional differentiation compared with T cells stimulated by a vaccine. Thus, the potency of the T cell response to histoincompatible tissue is likely due to many small T cell populations responding weakly to hundreds of MHC-bound peptides from graft-derived leukocytes.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allografts / immunology*
  • Animals
  • Graft Rejection / immunology*
  • Histocompatibility Antigens / chemistry
  • Histocompatibility Antigens / immunology*
  • Histocompatibility Antigens / metabolism
  • Immunophenotyping
  • Leukocytes / immunology*
  • Leukocytes / metabolism
  • Mice
  • Mice, Knockout
  • Peptides / chemistry
  • Peptides / immunology*
  • Peptides / metabolism
  • Protein Binding / immunology
  • Protein Multimerization
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism
  • T-Lymphocytes / immunology*

Substances

  • Histocompatibility Antigens
  • Peptides