LPS promotes CB3-induced myocarditis in resistant B10.A mice

James R. Lane, David A. Neumann, Anne Lafond-Walker, Ahvie Herskowitz, Noel R. Rose

Research output: Contribution to journalArticlepeer-review

Abstract

Coxsackie virus B3 (CB3) infection of A/J or A.SW mice results in autoimmune myocarditis characterized by a diffuse mononuclear cell infiltrate and heart-specific autoantibodies. C57BL/10 congenic mice that are identically treated are resistant to this disease. CB3-infected resistant B10.A mice were treated with LPS to determine if this immunomodulator alters disease susceptibility. In contrast to mice infected only with CB3 or treated only with LPS, CB3-infected/LPS-treated (CB3/LPS) B10.A mice developed autoimmune myocarditis similar to that observed in susceptible A/J or A.SW mice. By Day 14, CB3/LPS-induced disease was characterized by significant mortality, myocardial immunoglobulin deposition, and mononuclear cell infiltration of the heart. Immunohistochemical examination revealed deposits of IgG in the heart tissue and serum IgG autoantibodies reactive with sarcolemmal and fibrillary antigens in normal heart tissue. This serum IgG reacted with normal mouse cardiac antigens of a wide range of molecular weights by Western immunoblotting. Because LPS treatment is capable of increasing cytokine levels as well as MHC Class I and Class II expression in heart tissue, it suggests that these factors may contribute to susceptibility to autoimmune myocarditis in CB3-infected mice.

Original languageEnglish (US)
Pages (from-to)219-233
Number of pages15
JournalCellular Immunology
Volume136
Issue number1
DOIs
StatePublished - Aug 1991

ASJC Scopus subject areas

  • Immunology

Fingerprint

Dive into the research topics of 'LPS promotes CB3-induced myocarditis in resistant B10.A mice'. Together they form a unique fingerprint.

Cite this