4.7 Article

Absence of Cross-Presenting Cells in the Salivary Gland and Viral Immune Evasion Confine Cytomegalovirus Immune Control to Effector CD4 T Cells

Journal

PLOS PATHOGENS
Volume 7, Issue 8, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.ppat.1002214

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Funding

  1. Eidgenoessische Technische Hochschule Zurich
  2. Roche Research Foundation
  3. Swiss National Science Foundation [310030-129751]
  4. Deutsche Forschungsgemeinschaft [He2526/7-2]
  5. Swiss National Science Foundation (SNF) [310030_129751] Funding Source: Swiss National Science Foundation (SNF)

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Horizontal transmission of cytomegaloviruses (CMV) occurs via prolonged excretion from mucosal surfaces. We used murine CMV (MCMV) infection to investigate the mechanisms of immune control in secretory organs. CD4 T cells were crucial to cease MCMV replication in the salivary gland (SG) via direct secretion of IFN gamma that initiated antiviral signaling on non-hematopoietic cells. In contrast, CD4 T cell helper functions for CD8 T cells or B cells were dispensable. Despite SG-resident MCMV-specific CD8 T cells being able to produce IFN gamma, the absence of MHC class I molecules on infected acinar glandular epithelial cells due to viral immune evasion, and the paucity of cross-presenting antigen presenting cells (APCs) prevented their local activation. Thus, local activation of MCMV-specific T cells is confined to the CD4 subset due to exclusive presentation of MCMV-derived antigens by MHC class II molecules on bystander APCs, resulting in IFN gamma secretion interfering with viral replication in cells of non-hematopoietic origin.

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