High-frequency alloreactive T cells augment effector function of low-frequency CD8+ T-cell responses under CD28/CD154 blockade

Transplantation. 2010 May 27;89(10):1208-17. doi: 10.1097/TP.0b013e3181df53dc.

Abstract

Background: Blockade of costimulatory molecules is a potent method of inducing long-term graft survival. We have previously addressed the issue of donor-reactive T-cell precursor frequency on relative costimulation dependence and found that the presence of a high precursor frequency of donor-reactive CD8 T cells resulted in costimulation blockade-resistant graft rejection, whereas the presence of a low-frequency donor-reactive population did not. To address the mechanisms by which high-frequency T cells obviated the requirement for costimulation, we asked whether a low-frequency population responding concomitantly with a high-frequency response also demonstrated costimulation independence.

Methods: A model system was established in which B6 mice containing a low frequency of anti-membrane bound chicken ovalbumin (mOVA) responders and a high frequency of anti-BALB/c responders received a skin graft from B6.mOVAxBALB/c F1 donors in the presence or absence of cytotoxic T-lymphocyte antigen-4 Ig/anti-CD154 costimulatory blockade.

Results: The results revealed that in the presence of costimulation blockade, high-frequency anti-BALB/c T cells augmented the effector activity of low-frequency anti-mOVA T cells, but it did not enhance the accumulation of anti-mOVA T cells capable of mediating graft rejection.

Conclusions: These results demonstrate that both antigen-specific and antigen-independent factors contribute to the relative costimulation independence of high-frequency T-cell responses.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adoptive Transfer
  • Animals
  • Antibodies, Monoclonal
  • CD8-Positive T-Lymphocytes / immunology
  • Epitopes / immunology
  • Flow Cytometry
  • Graft Rejection / immunology
  • Graft Rejection / pathology
  • Graft Survival / immunology
  • Graft Survival / physiology
  • Lymphocyte Culture Test, Mixed
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Inbred Strains
  • Ovalbumin / pharmacology
  • Skin Transplantation / immunology*
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / immunology*
  • Transcriptional Activation
  • Transplantation, Homologous / immunology
  • Transplantation, Homologous / pathology

Substances

  • Antibodies, Monoclonal
  • Epitopes
  • Ovalbumin