Rev activity determines sensitivity of HIV-1-infected primary T cells to CTL killing

被引:36
作者
Bobbitt, KR
Addo, MM
Altfeld, M
Filzen, T
Onafuwa, AA
Walker, BD
Collins, KL
机构
[1] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
[3] Massachusetts Gen Hosp, Ctr AIDS Res, Charlestown, MA 02114 USA
[4] Massachusetts Gen Hosp, Infect Dis Unit, Charlestown, MA 02114 USA
关键词
D O I
10.1016/S1074-7613(03)00031-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The HIV Nef protein is thought to promote HIV immune evasion by downmodulating MHC-I and protecting infected cells from CTL killing. In addition, we demonstrated that Rev, an HIV regulatory protein needed for expression of the HIV late genes, can influence CTL killing. When Rev activity level was reduced by virtue of amino acid alterations in the Rev protein sequence, infected cells were more resistant to anti-Gag and anti-Env CTL killing. A screen of primary viral isolates revealed that viruses derived from asymptomatic, infected people had lower Rev activity, lower Gag levels, and greater resistance to anti-Gag CTL killing. Thus, rev alleles with low activity may have a selective advantage in infected people with effective immune responses.
引用
收藏
页码:289 / 299
页数:11
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