Reduction in CD8 + cell noncytotoxic anti-HIV activity in individuals receiving highly active antiretroviral therapy during primary infection
Recent advances in the ability to detect people at the early stages of HIV infection now permit the initiation of antiretroviral treatment before the full complement of antiviral immune responses has evolved. However, the influence of early treatment interventions on the developing anti-HIV immune r...
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Published in | Proceedings of the National Academy of Sciences - PNAS Vol. 98; no. 2; pp. 597 - 602 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
16.01.2001
|
Online Access | Get full text |
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Summary: | Recent advances in the ability to detect people at the early
stages of HIV infection now permit the initiation of antiretroviral
treatment before the full complement of antiviral immune responses has
evolved. However, the influence of early treatment interventions on the
developing anti-HIV immune response is unknown. This study investigates
the impact of standard highly active antiretroviral therapy (HAART)
during the primary stages of HIV infection on the plasma HIV-1 RNA
level, CD4
+
and CD8
+
lymphocyte counts, and the
CD8
+
cell anti-HIV response. Individuals treated with HAART
within 6 months of infection showed dramatic and rapid reductions in
HIV-1 RNA levels along with modest increases in CD4
+
cell
number and decreases in CD8
+
cell numbers. A significant
reduction in the level of CD8
+
cell noncytotoxic
suppression of HIV replication was observed over time in most
participants receiving HAART. Importantly, those individuals choosing
not to receive therapy maintained low but detectable HIV-1 RNA levels
and showed no reduction in their CD8
+
cell antiviral
response. These results suggest that either continued antigenic
challenge is required to sustain CD8
+
cell-mediated
anti-HIV activity, or that HAART has some inhibitory effect on this
important immunologic function during the early stages of infection. |
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ISSN: | 0027-8424 1091-6490 |
DOI: | 10.1073/pnas.98.2.597 |