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Published online before print June 24, 2004

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© by The Society for Leukocyte Biology
Journal of Leukocyte Biology, doi:10.1189/jlb.0404234

Received for publication April 12, 2004.

Accepted for publication May 14, 2004.

Article

HIV-1 compartmentalization in diverse leukocyte populations during antiretroviral therapy

Simon J. Potter ^*, Phillipe Lemey , Guillaume Achaz , Choo Beng Chew , Anne-Mieke Vandamme , Dominic E. Dwyer , and Nitin K. Saksena ^*@

*Center for Virus Research, Westmead Millennium Institute and The University of Sydney, Australia; Department of Virology, Center for Infectious Diseases and Microbiology Laboratory Services, ICPMR, Westmead Hospital, Sydney, Australia; Clinical and Epidemiological Virology, Rega Institute for Medical Research, Leuven, Belgium; and 2102 Biological Laboratories, Harvard University, Cambridge, Massachusetts

^@ To whom correspondence should be addressed. E-mail: nitin_saksena{at}wmi.usyd.edu.au.

	Abstract

CD4⁺ T lymphocytes are the primary target of human immunodeficiency virus type 1 (HIV-1), but there is increasing evidence that other immune cells in the blood, including CD8⁺ T lymphocytes and monocytes, are also productively infected. The extent to which these additional cellular reservoirs contribute to ongoing immunodeficiency and viral persistence during therapy remains unclear. In this study, we conducted a detailed investigation of HIV-1 diversity and genetic structure in CD4⁺ T cells, CD8⁺ T cells, and monocytes of 13 patients receiving highly active antiretroviral therapy (HAART). Analysis of molecular variance and nonparametric tests performed on HIV-1 envelope sequences provided statistically significant evidence of viral compartmentalization in different leukocyte populations. Signature pattern analysis and predictions of coreceptor use provided no evidence that selection arising from viral tropism was responsible for the genetic structure observed. Analysis of viral genetic variation in different leukocyte populations demonstrated the action of founder effects as well as significant variation in the extent of genetic differentiation between subpopulations among patients. In the absence of evidence for leukocyte-specific selection, these features were supportive of a metapopulation model of HIV-1 replication as described previously among HIV-1 populations in the spleen. Compartmentalization of the virus in different leukocytes may have significant implications for current models of HIV-1 population genetics and contribute to the highly variable way in which drug resistance evolves in different individuals during HAART.

Key Words: HAART • HIV-1 population genetics • CD4⁺ T lymphocytes • CD8⁺ T lymphocytes • monocytes

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