共 65 条
Antibody-based inhibitors of HIV infection
被引:11
作者:

Choudhry, Vidita
论文数: 0 引用数: 0
h-index: 0
机构: NCI Frederick, Prot Interact Grp, CCRNP, CCR,NIH, Frederick, MD 21702 USA

Zhang, Mei-Yun
论文数: 0 引用数: 0
h-index: 0
机构: NCI Frederick, Prot Interact Grp, CCRNP, CCR,NIH, Frederick, MD 21702 USA

Dimitrova, Dimana
论文数: 0 引用数: 0
h-index: 0
机构: NCI Frederick, Prot Interact Grp, CCRNP, CCR,NIH, Frederick, MD 21702 USA

Prabakaran, Ponraj
论文数: 0 引用数: 0
h-index: 0
机构: NCI Frederick, Prot Interact Grp, CCRNP, CCR,NIH, Frederick, MD 21702 USA

Dimitrov, Antony S.
论文数: 0 引用数: 0
h-index: 0
机构: NCI Frederick, Prot Interact Grp, CCRNP, CCR,NIH, Frederick, MD 21702 USA

Fouts, Timothy R.
论文数: 0 引用数: 0
h-index: 0
机构: NCI Frederick, Prot Interact Grp, CCRNP, CCR,NIH, Frederick, MD 21702 USA

Dimitrov, Dimiter S.
论文数: 0 引用数: 0
h-index: 0
机构: NCI Frederick, Prot Interact Grp, CCRNP, CCR,NIH, Frederick, MD 21702 USA
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
相关论文
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