Targeted cytotoxic therapy: adapting a rapidly progressing anticancer paradigm for depletion of persistent HIV-infected cell reservoirs

被引:13
作者
Berger, Edward A. [1 ]
机构
[1] NIAID, Viral Dis Lab, NIH, Bethesda, MD 20892 USA
关键词
adoptive cell therapy; antibody-drug conjugates; chimeric antigen receptor; immunotoxin; oncolytic virotherapy; radioimmunotherapy; targeted liposome; HUMAN-IMMUNODEFICIENCY-VIRUS; ACTIVE ANTIRETROVIRAL THERAPY; T-CELLS; VIRAL RESERVOIRS; RECEPTOR; SURVIVAL; ELIMINATION; LYMPHOCYTES; VIREMIA; CD4(+);
D O I
10.1097/COH.0b013e3283412515
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Purpose of review HIV-infected cells persisting in the face of highly active antiretroviral therapy are arguably the greatest hurdle to eradication of the virus from the body. Complementary strategies aimed at selective killing of infected cells are described. Recent findings Pioneered by research in the cancer field, various approaches are under development for selective killing of HIV-infected cells. These include targeted cytotoxic proteins, adoptive cell therapy, cytocidal virotherapy, and targeted nonbiological drug carriers. Summary These developmental efforts may provide a critical complement to antiretroviral therapy in efforts to achieve HIV eradication, or a 'functional cure' whereby therapy can be stopped without viral rebound.
引用
收藏
页码:80 / 85
页数:6
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