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Journal of Virology, May 2009, p. 4700-4703, Vol. 83, No. 9
0022-538X/09/$08.00+0 doi:10.1128/JVI.02240-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Center for Vaccines and Immunity, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio 43205,1 College of Medicine, The Ohio State University, Columbus, Ohio 432102
Received 23 October 2008/ Accepted 16 February 2009
CD4 T cells are critical for the control of gammaherpesvirus persistence, but their direct effector mechanisms of virus control in vivo are still poorly understood. In this study, we use murine gammaherpesvirus 68 (
HV68) in in vitro and in vivo cytotoxicity assays to show CD4-dependent killing of
HV68-loaded cells in mice persistently infected with
HV68. Our results underscore the cytotoxic capacity of CD4 T cells during
HV68 persistence.
Published ahead of print on 25 February 2009.
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