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Journal of Virology, May 2001, p. 4435-4438, Vol. 75, No. 9
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.9.4435-4438.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Virus-Specific and Bystander CD8+
T-Cell Proliferation in the Acute and Persistent Phases of a
Gammaherpesvirus Infection
Gabrielle T.
Belz
and
Peter C.
Doherty*
Department of Immunology, St. Jude
Children's Research Hospital, Memphis, Tennessee 38105
Received 21 November 2000/Accepted 29 January 2001
The cycling characteristics of CD8+ T cells specific
for two lytic-phase epitopes of murine gammaherpesvirus 68 (
HV68)
have been analyzed for mice with high or low levels of virus
persistence. The extent of cell division is generally reflective of the
antigen load and suggests that
HV68 may be regularly reactivating
from latency for some months after the resolution of the acute phase of
the infectious process. Although
HV68 infection is also associated with massive proliferation of lymphocytes that are not obviously specific for the virus, the level of "bystander-induced" cycling in
a population of influenza virus-specific CD8+ T cells was
generally fourfold lower than the extent of cell division seen
for the antigen-driven,
HV68-specific response. The overall
conclusion is that turnover rates substantially in excess of 5 to 10%
over 6 days for CD8+ "memory" T-cell populations are
likely to be reflective of continued antigenic exposure.
*
Corresponding author. Mailing address: Department of
Immunology, St. Jude Children's Research Hospital, 332 North
Lauderdale, Memphis, TN 38105. Phone: (901) 495-3470. Fax: (901)
495-3107. E-mail: peter.doherty{at}stjude.org.

Present address: Division of Immunology, The Walter and Eliza Hall
Institute of Medical Research, Royal Melbourne Hospital,
Melbourne, Victoria 3050,
Australia.
Journal of Virology, May 2001, p. 4435-4438, Vol. 75, No. 9
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.9.4435-4438.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
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