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Journal of Virology, June 2005, p. 6808-6813, Vol. 79, No. 11
0022-538X/05/$08.00+0 doi:10.1128/JVI.79.11.6808-6813.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Is Not Essential for T-Cell-Mediated Clearance of Murine Gammaherpesvirus 68
Ashley B. Lyon,
Mark D. Wareing,
Peter B. Dias,
and
Sally R. Sarawar*
Division of Molecular Immunology, La Jolla Institute for Allergy and Immunology, 10355 Science Center Drive, San Diego, California 92121
Received 2 November 2004/ Accepted 18 January 2005
Murine gammaherpesvirus 68 (MHV-68) is a naturally occurring rodent pathogen with significant homology to human pathogens Epstein-Barr virus and Kaposi's sarcoma-associated herpesvirus. T cells are essential for primary clearance of MHV-68 and survival of mice following intranasal infection. Previous reports have suggested that protein kinase C
(PKC
) is essential for T-cell activation and cytokine production in vitro. To determine the role of this molecule in vivo during the immune response to a viral infection, PKC
/ mice were infected with MHV-68. Despite the essential role of T cells in viral clearance, PKC
/ mice survived infection, cleared lytic virus, and maintained effective long-term control of latency. CD8 T-cell expansion, trafficking to the lung, and cytotoxic activity were similar in PKC
+/+ and PKC
/ mice, whereas antiviral antibody and T-helper cell cytokine production were significantly lower in PKC
/ mice than in PKC
+/+ mice. These studies demonstrate a differential requirement for PKC
in the immune response to MHV-68 and show that PKC
is not essential for the T-cell activation events leading to viral clearance.
Present address: Viral Immunology, Torrey Pines Institute for Molecular Studies, 3550 General Atomics Court, San Diego, CA 92121.
Present address: Department of Medicine, Karolinska Institute, Huddinge University Hospital, SE-141 86 Stockholm, Sweden.
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