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Journal of Virology, October 1999, p. 8435-8440, Vol. 73, No. 10
Laboratory of Persistent Viral Diseases, Rocky
Mountain Laboratories, National Institute of Allergy and Infectious
Diseases, National Institutes of Health, Hamilton, Montana 59840
Received 26 April 1999/Accepted 21 June 1999
Vaccination of mice with a live attenuated vaccine virus induces
potent protection against subsequent challenge with pathogenic Friend
retroviral complex. The kinetic studies presented here demonstrate
protection from acute splenomegaly as early as 1 week postvaccination.
At this time point virus-specific cytotoxic T lymphocytes (CTL) were
demonstrable in direct chromium release assays. However, during the
first 2 weeks after vaccination protection was incomplete since the
mice were not protected against establishment of low-level persistent
infections in the spleen. By 3 weeks postvaccination the animals were
protected against the establishment of persistent virus as well as
acute splenomegaly. The timing of this complete protection correlated
with the presence of both virus-neutralizing antibodies and primed CTL
in the immunized mice. Within 3 days of virus challenge, vaccinated
mice showed high levels of activated B cells and CD4+ and
CD8+ T cells, indicating an efficient priming of all
lymphocyte subsets. Despite very limited replication of the vaccine
virus, the protective effect was long lived and was still present 6 months after immunization.
0022-538X/99/$04.00+0
Kinetics of the Development of Protective Immunity
in Mice Vaccinated with a Live Attenuated Retrovirus

*
Corresponding author. Mailing address: Laboratory of
Persistent Viral Diseases, Rocky Mountain Laboratories, National
Institute of Allergy and Infectious Diseases, National Institutes of
Health, 903 S. 4th St., Hamilton, MT 59840. Phone: (406) 363-9310. Fax: (406) 363-9286. E-mail: khasenkrug{at}nih.gov.
Present address: Institut für Virologie, 97078 Würzburg, Germany.
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