Stimulation of HIV-1-Specific Cytolytic T Lymphocytes Facilitates Elimination of Latent Viral Reservoir after Virus Reactivation

被引:629
作者
Shan, Liang [1 ,2 ]
Deng, Kai [1 ]
Shroff, Neeta S. [1 ]
Durand, Christine M. [1 ]
Rabi, S. Alireza. [1 ]
Yang, Hung-Chih [3 ]
Zhang, Hao [4 ]
Margolick, Joseph B. [4 ]
Blankson, Joel N. [1 ]
Siliciano, Robert F. [1 ,5 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Pharmacol & Mol Sci, Baltimore, MD 21205 USA
[3] Natl Taiwan Univ, Coll Med, Dept Microbiol, Taipei 100, Taiwan
[4] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Mol Microbiol & Immunol, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Sch Med, Howard Hughes Med Inst, Baltimore, MD 21205 USA
关键词
ACTIVE ANTIRETROVIRAL THERAPY; IN-VITRO SYSTEM; HIV-INFECTION; VALPROIC ACID; HIV-1-INFECTED PATIENTS; CYTOTOXIC LYMPHOCYTES; IMMUNOLOGICAL CONTROL; GENE-EXPRESSION; CELL DEPLETION; VIREMIA;
D O I
10.1016/j.immuni.2012.01.014
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Highly active antiretroviral therapy (HAART) suppresses HIV-1 replication but cannot eliminate the virus because HIV-1 establishes latent infection. Interruption of HAART leads to a rapid rebound of viremia, so life-long treatment is required. Efforts to purge the latent reservoir have focused on reactivating latent proviruses without inducing global T cell activation. However, the killing of the infected cells after virus reactivation, which is essential for elimination of the reservoir, has not been assessed. Here we show that after reversal of latency in an in vitro model, infected resting CD4(+) T cells survived despite viral cytopathic effects, even in the presence of autologous cytolytic T lymphocytes (CTLs) from most patients on HAART. Antigen-specific stimulation of patient CTLs led to efficient killing of infected cells. These results demonstrate that stimulating HIV-1-specific CTLs prior to reactivating latent HIV-1 may be essential for successful eradication efforts and should be considered in future clinical trials.
引用
收藏
页码:491 / 501
页数:11
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