| Literature DB >> 11986671 |
Daniel C Douek1, Jason M Brenchley, Michael R Betts, David R Ambrozak, Brenna J Hill, Yukari Okamoto, Joseph P Casazza, Janaki Kuruppu, Kevin Kunstman, Steven Wolinsky, Zvi Grossman, Mark Dybul, Annette Oxenius, David A Price, Mark Connors, Richard A Koup.
Abstract
HIV infection is associated with the progressive loss of CD4(+) T cells through their destruction or decreased production. A central, yet unresolved issue of HIV disease is the mechanism for this loss, and in particular whether HIV-specific CD4(+) T cells are preferentially affected. Here we show that HIV-specific memory CD4(+) T cells in infected individuals contain more HIV viral DNA than other memory CD4(+) T cells, at all stages of HIV disease. Additionally, following viral rebound during interruption of antiretroviral therapy, the frequency of HIV viral DNA in the HIV-specific pool of memory CD4(+) T cells increases to a greater extent than in memory CD4(+) T cells of other specificities. These findings show that HIV-specific CD4(+) T cells are preferentially infected by HIV in vivo. This provides a potential mechanism to explain the loss of HIV-specific CD4(+) T-cell responses, and consequently the loss of immunological control of HIV replication. Furthermore, the phenomenon of HIV specifically infecting the very cells that respond to it adds a cautionary note to the practice of structured therapy interruption.Entities:
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Year: 2002 PMID: 11986671 DOI: 10.1038/417095a
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962