Cellular immune mechanisms in Coxsackievirus group B, type 3 induced myocarditis in Balb/C mice

Adv Exp Med Biol. 1983:161:491-508. doi: 10.1007/978-1-4684-4472-8_29.

Abstract

Coxsackie B viruses are a common cause of viral myocarditis in humans. A murine model of the human disease has been developed using Coxsackievirus group B, type 3 and inbred Balb/c mice. Infection of T lymphocyte deficient mice does not result in significant myocarditis indicating the importance of T cells in this disease. The virus can be isolated from the hearts of T cell deficient and normal mice in equal concentrations. Virus elimination presumably is mediated by virus specific neutralizing antibody induced in both groups. T lymphocytes, natural killer cells and macrophage obtained from normal virus infected mice are all capable of lysing myofibers in vitro. Maximum lysis is obtained with the cytolytic T cells. When these cell populations or Coxsackievirus immune antibody were adoptively transferred into T lymphocyte deficient animals infected with the virus, only animals given T cells developed significant myocarditis.

Publication types

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

MeSH terms

  • Animals
  • Coxsackievirus Infections / immunology*
  • Coxsackievirus Infections / pathology
  • Cytotoxicity, Immunologic
  • Enterovirus B, Human / immunology
  • Immunity, Cellular
  • Kinetics
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred CBA
  • Myocarditis / etiology
  • Myocarditis / immunology*
  • Myocardium / immunology
  • Radiation Chimera
  • Spleen / cytology
  • Spleen / immunology
  • T-Lymphocytes / immunology