Journal
JOURNAL OF VIROLOGY
Volume 78, Issue 18, Pages 10096-10103Publisher
AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.78.18.10096-10103.2004
Keywords
-
Categories
Funding
- NCRR NIH HHS [R01 RR006555, RR06555] Funding Source: Medline
- NIAID NIH HHS [AI28433, R37 AI028433, R01 AI028433] Funding Source: Medline
Ask authors/readers for more resources
Several primate models indicate that cytotoxic T lymphocyte-inducing vaccines may be unable to prevent human immunodeficiency virus infection but may have a long-term benefit in controlling viral replication and delaying disease progression. Here we show that analysis of the kinetics of antigen-specific CD8(+) T-cell expansion suggests a delay in activation following infection that allows unimpeded early viral replication. Viral kinetics do not differ between controls and vaccinees during this delay phase. An increase in virus-specific CD8(+) T-cell numbers around day 10 postinfection coincides with a slowing in viral replication in vaccinees and reduces peak viral loads by around I log. However, this response is too little too late to prevent establishment of persistent infection.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available