Abstract:
:We have previously described a selective increase in HIV-DNA content in CCR5-negative lymphocytes from late stage HIV-infected patients. Here, we show that this increase occurred even in the absence of viral phenotypic switching from CCR5- to CXCR4-tropic. This leads us to hypothesize that early and late CCR5-tropic viruses might be different in the ability to infect CCR5-low or -negative cells. We compared a set of early CCR5-tropic viruses with low viral DNA content in CCR5-negative cells to a set of late CCR5-tropic viruses with high viral DNA content in CCR5-negative cells. We could not find any significant differences between the two sets of viruses in the aspects of relative infectivity in CCR5-low cells and the level of inhibition by beta-chemokine. This suggested that there may be some changes in cellular phenotype or environment that allows an expansion of susceptible cell population in late stages HIV infection. Understanding these changes may provide a novel approach for HIV therapy.
journal_name
Virologyjournal_title
Virologyauthors
Pakarasang M,Wasi C,Suwanagool S,Chalermchockcharoenkit A,Auewarakul Pdoi
10.1016/j.virol.2005.12.003subject
Has Abstractpub_date
2006-04-10 00:00:00pages
372-8issue
2eissn
0042-6822issn
1096-0341pii
S0042-6822(05)00807-Xjournal_volume
347pub_type
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