Prevalence of CD8(+)alpha beta T cells in Trypanosoma cruzi-elicited myocarditis is associated with acquisition of CD62L(Low)LFA-1(High)VLA-4(High) activation phenotype and expression of IFN-gamma-inducible adhesion and chemoattractant molecules

Microbes Infect. 2001 Oct;3(12):971-84. doi: 10.1016/s1286-4579(01)01461-7.

Abstract

The determinants of the prevalence of CD8(+) T cells in the inflamed myocardium of Trypanosoma cruzi-infected patients and experimental animals are undefined. Using C3H/He mice infected with the Colombiana strain of T. cruzi, we found that the distribution of CD4(+)/CD8(-) and CD4(-)/CD8(+) T cells in the myocardium mirrors the frequency of cells expressing the CD62L(Low)LFA-1(High)VLA-4(High) activation phenotype among CD4(+)/CD8(-) and CD4(-)/CD8(+ )peripheral blood T cells. Consistently, vascular cell adhesion molecule-1-positive endothelial cells and a fine fibronectin network surrounding VLA-4(+) mononuclear cells were found in the inflamed myocardium. Further, interferon gamma (IFN-gamma) and IFN-gamma-induced chemokines (RANTES, MIG and CRG-2/IP-10), as well as JE/MCP-1 and MIP1-alpha, were found to be the dominant cytokines expressed in situ during acute and chronic myocarditis elicited by T. cruzi. In contrast, interleukin 4 mRNA was only detected during the chronic phase. Altogether, the results indicate that the distribution of T-cell subsets in the myocardium of T. cruzi-infected mice reflects the particular profile of adhesion molecules acquired by most peripheral CD8(+) T lymphocytes and point to the possibility that multiple IFN-gamma-inducible molecules present in the inflamed tissue contribute to the establishment and maintenance of T. cruzi-induced myocarditis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD8-Positive T-Lymphocytes / immunology*
  • Cell Adhesion Molecules / biosynthesis
  • Chagas Cardiomyopathy / immunology*
  • Chagas Cardiomyopathy / parasitology
  • Chagas Cardiomyopathy / pathology
  • Chemokines / biosynthesis
  • Cytokines / biosynthesis
  • Female
  • Immunophenotyping
  • Integrin alpha4beta1
  • Integrins / analysis*
  • Interferon-gamma / pharmacology*
  • L-Selectin / analysis*
  • Lymphocyte Function-Associated Antigen-1 / analysis*
  • Mice
  • Mice, Inbred C3H
  • Myocardium / pathology
  • Parasitemia / mortality
  • Receptors, Antigen, T-Cell, alpha-beta / analysis*
  • Receptors, Lymphocyte Homing / analysis*

Substances

  • Cell Adhesion Molecules
  • Chemokines
  • Cytokines
  • Integrin alpha4beta1
  • Integrins
  • Lymphocyte Function-Associated Antigen-1
  • Receptors, Antigen, T-Cell, alpha-beta
  • Receptors, Lymphocyte Homing
  • L-Selectin
  • Interferon-gamma