In vivo migration and function of transferred HIV-1-specific cytotoxic T cells

被引:271
作者
Brodie, SJ
Lewinsohn, DA
Patterson, BK
Jiyamapa, D
Krieger, J
Corey, L
Greenberg, PD
Riddell, SR
机构
[1] Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USA
[2] Univ Washington, Dept Lab Med, Seattle, WA 98101 USA
[3] Univ Washington, Dept Pediat, Seattle, WA 98101 USA
[4] Univ Washington, Dept Urol, Seattle, WA 98101 USA
[5] Univ Washington, Dept Med, Seattle, WA 98101 USA
[6] Univ Washington, Dept Immunol, Seattle, WA 98101 USA
[7] Northwestern Univ, Sch Med, Dept Obstet & Gynecol, Foster City, CA 94404 USA
关键词
D O I
10.1038/4716
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The persistence of HIV replication in infected individuals may reflect an inadequate host HIV-specific CD8(+) cytotoxic T lymphocyte (CTL) response. The functional activity of HIV-specific CTLs and the ability of these effector cells to migrate in vivo to sites of infection was directly assessed by expanding autologous HIV-1 Gag-specific CD8(+) CTL clones in vitro and adoptively transferring these CTLs to HIV-infected individuals, The transferred CTLs retained lytic function in vivo, accumulated adjacent to HIV-infected cells in lymph nodes and transiently reduced the levels of circulating productively infected CD4(+) T cells. These results provide direct evidence that HIV-specific CTLs target sites of HIV replication and mediate antiviral activity, and indicate that the development of immunotherapeutic approaches to sustain a strong CTL response to HIV may be a useful adjunct to treatment of HIV infection.
引用
收藏
页码:34 / 41
页数:8
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