Primary Clearance of Murine Gammaherpesvirus 68 by PKCθ −/− CD8 T Cells Is Compromised in the Absence of Help from CD4 T Cells

Author:

Dias Peter1,Shea Ashley L.1,Inglis Chandra1,Giannoni Francesca1,Lee Lian Ni1,Sarawar Sally R.1

Affiliation:

1. Torrey Pines Institute for Molecular Studies, 3550 General Atomics Court, San Diego, California 92121

Abstract

ABSTRACT CD4 T cells are dispensable for acute control of murine gammaherpesvirus 68 (MHV-68) but are necessary for effective long-term control of the virus by CD8 T cells. In contrast, protein kinase C θ (PKCθ) is not essential for either acute or long-term viral control. However, we found that while either CD4 or CD8 T cells could mediate the clearance of MHV-68 from the lungs of PKCθ +/+ mice, PKCθ −/− mice depleted of either subset failed to clear the virus. These data suggest that there are two alternative pathways for MHV-68 clearance, one dependent on CD4 T cells and the other on PKCθ. Protection mediated by the latter appears to be short-lived. These observations may help to explain the differential requirement for PKCθ in various models of CD8 T-cell activation and differences in the costimulatory requirements for acute and long-term viral control.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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