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Continued evolution of HIV‐1 circulating in blood monocytes with antiretroviral therapy: genetic analysis of HIV‐1 in monocytes and CD4+ T cells of patients with discontinued therapy
Author(s) -
Llewellyn Nick,
Zioni Rafael,
Zhu Haiying,
Andrus Thomas,
Xu Youg,
Corey Lawrence,
Zhu Tuofu
Publication year - 2006
Publication title -
journal of leukocyte biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.819
H-Index - 191
eISSN - 1938-3673
pISSN - 0741-5400
DOI - 10.1189/jlb.0306144
Subject(s) - compartmentalization (fire protection) , biology , monocyte , human immunodeficiency virus (hiv) , immunology , antiretroviral therapy , viral replication , virology , viral load , virus , enzyme , biochemistry
The role of blood monocytes in HIV‐1 infection is a relatively new field of interest. What happens to HIV‐1 in monocytes and their relationship to CD4+ T cells before, during, and after suppressive antiretroviral therapy (ART) is largely unstudied. Here, considering that diversity is a good indicator of continued replication over time, we evaluated the effect of ART on HIV‐1 in blood monocytes and CD4+ T cells by examining the diversity of HIV‐1 from 4 infected patients who underwent and stopped therapy. We determined diversity and compartmentalization of HIV‐1 between blood monocytes and CD4+ T cells in each patient in relationship to their ART regimens. Our data indicate that the rate of HIV‐1 diversity increase in monocytes during therapy was significantly higher than in CD4+ T cells ( P <0.05), suggesting that HIV‐1 present in monocytes diversify more during therapy than in CD4+ T cells. Increased rates of HIV‐1 compartmentalization between monocytes and CD4+ T cells while on therapy were also observed. These results suggest that ART inhibits HIV‐1 replication in CD4+ T cells more than in blood monocytes and that better treatments to combat HIV‐1 in monocytes/macrophages may be needed for a more complete suppression of HIV replication.