Antibody-based inhibitors of HIV infection

被引:11
作者
Choudhry, Vidita
Zhang, Mei-Yun
Dimitrova, Dimana
Prabakaran, Ponraj
Dimitrov, Antony S.
Fouts, Timothy R.
Dimitrov, Dimiter S.
机构
[1] NCI Frederick, Prot Interact Grp, CCRNP, CCR,NIH, Frederick, MD 21702 USA
[2] SAIC Frederick Inc, BRP, NCI Frederick, Frederick, MD 21702 USA
[3] Uniformed Serv Univ Hlth Sci, Dept Microbiol & Immunol, Bethesda, MD 20814 USA
[4] UMBC, Techctr, Profectus BioSci Inc, Baltimore, MD 21227 USA
关键词
antibody therapeutics; envelope glycoprotein; fusion; HIV; neutralisation; vaccine;
D O I
10.1517/14712598.6.5.523
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The demand for new treatment options against HIV is becoming increasingly desperate as the side effects and the expansion and spread of drug-resistant virus within the infected population limit the clinical benefits provided by available anti-HIV drugs. Preparations of polyclonal antibodies have a long history of proven clinical utility against some viruses; however, they have enjoyed very limited success against HIV. Recent clinical trials and in vitro experiments suggest that monoclonal antibodies against HIV may have promise clinically. These antibodies and antibody-based reagents target either the viral envelope glycoprotein, the receptor (CD4) or coreceptor (CCR5) molecules, or transition-state structures that appear during viral entry. The challenge is whether an antibody-based therapy can be identified (with or without their small molecule brethren) that presents long-term clinical efficacy, low toxicity and minimal risk of clinical failure from viral resistance.
引用
收藏
页码:523 / 531
页数:9
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