SIV-associated myocarditis: viral and cellular correlates of inflammation severity

AIDS Res Hum Retroviruses. 2006 Jun;22(6):529-40. doi: 10.1089/aid.2006.22.529.

Abstract

Myocarditis is a common finding in HIV-infected people. Cardiac inflammatory lesions and functional abnormalities similar to those documented in HIV infection are frequently seen in SIV infection of rhesus monkeys, suggesting a shared disease mechanism. A retrospective analysis of cardiac tissue collected at necropsy was performed to assess correlates of myocardial inflammation in SIV-infected rhesus monkeys. Intramyocardial SIV-infected cells were identified in 7 of 21 hearts from SIV-infected animals, with viral protein consistently colocalizing with the macrophage marker HAM 56. Productively infected cells occurred in low numbers, and did not correlate with the presence or quantity of inflammation or necrosis. Intramyocardial CMV was identified in 6 of 21 hearts from SIV+ animals, but also did not correlate with the presence or quantity of inflammation or necrosis. In contrast, T cell infiltration correlated inversely with DC-SIGN+ cell numbers, which occurred in significantly higher numbers in SIV+ animals with histologically normal myocardium than in SIV+ animals with active or borderline myocarditis or in uninfected controls (p < 0.001), suggesting an important immunoregulatory role for this population within the myocardium.

Publication types

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

MeSH terms

  • Animals
  • Antibodies, Monoclonal
  • Cell Adhesion Molecules / metabolism
  • Heart / virology
  • Image Processing, Computer-Assisted
  • Inflammation / immunology
  • Inflammation / physiopathology*
  • Lectins, C-Type / metabolism
  • Macaca mulatta
  • Macrophages / metabolism
  • Myocarditis / immunology
  • Myocarditis / physiopathology*
  • Myocarditis / virology*
  • Receptors, Cell Surface / metabolism
  • Severity of Illness Index*
  • Simian Acquired Immunodeficiency Syndrome / complications*
  • Simian Immunodeficiency Virus / pathogenicity*
  • T-Lymphocytes / immunology
  • Viral Proteins / metabolism

Substances

  • Antibodies, Monoclonal
  • Cell Adhesion Molecules
  • DC-specific ICAM-3 grabbing nonintegrin
  • HAM-56 antibody
  • Lectins, C-Type
  • Receptors, Cell Surface
  • Viral Proteins