Antiretroviral drug-based microbicides to prevent HIV-1 sexual transmission

被引:137
作者
Masse, Per Johan [1 ]
Shattock, Robin [2 ]
Moore, John P. [1 ]
机构
[1] Cornell Univ, Weill Med Coll, Dept Microbiol & Immunol, New York, NY 10021 USA
[2] Univ London St Georges Hosp, London, England
来源
ANNUAL REVIEW OF MEDICINE | 2008年 / 59卷
关键词
topical application; vaginal rings; sustained-release formulations; reverse transcriptase inhibitors; entry inhibitors;
D O I
10.1146/annurev.med.59.061206.112737
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The development of a vaginal (and perhaps a rectal) microbicide would be of major benefit for slowing the global spread of human immunodeficiency virus type 1 (HIV-1). A microbicide is a gel or related device that, when inserted vaginally or rectally, acts to prevent infection of a woman or a man by HIV-1 during sexual intercourse. A practical microbicide must be not only effective, safe, and user-friendly but also economically affordable in the developing world. To date, the performance of microbicide candidates in efficacy trials has been disappointing, but next-generation concepts now in or approaching clinical trials offer improved prospects for efficacy. The most plausible approaches involve topical application of antirctroviral agents with specific activity against HIV-1, compounds similar to drugs used to treat HIV-1 infection. How these inhibitors are applied may also be critical, with sustained-release formulations and vaginal ring delivery systems now becoming a high priority.
引用
收藏
页码:455 / 471
页数:17
相关论文
共 70 条
[1]  
Anonymous, 2005, Antiviral Chemistry & Chemotherapy, V16, P339
[2]   Randomized, controlled intervention trial of male circumcision for reduction of HIV infection risk: The ANRS 1265 trial [J].
Auvert, B ;
Taljaard, D ;
Lagarde, E ;
Sobngwi-Tambekou, J ;
Sitta, M ;
Puren, A .
PLOS MEDICINE, 2005, 2 (11) :1112-1122
[3]   Inhibition of HIV entry by carbohydrate-binding proteins [J].
Balzarini, J. .
ANTIVIRAL RESEARCH, 2006, 71 (2-3) :237-247
[4]   Distribution of a spermicide containing Nonoxynol-9 in the vaginal canal and the upper female reproductive tract [J].
Barnhart, KT ;
Stolpen, A ;
Pretorius, ES ;
Malamud, D .
HUMAN REPRODUCTION, 2001, 16 (06) :1151-1154
[5]   Biologic and genetic characterization of a panel of 60 human immunodeficiency virus type 1 isolates, representing clades A, B, C, D, CRF01_AE, and CRF02_AG, for the development and assessment of candidate vaccines [J].
Brown, BK ;
Darden, JM ;
Tovanabutra, S ;
Oblander, T ;
Frost, J ;
Sanders-Buell, E ;
de Souza, MS ;
Birx, DL ;
McCutchan, FE ;
Polonis, VR .
JOURNAL OF VIROLOGY, 2005, 79 (10) :6089-6101
[6]   HIV vaccine design and the neutralizing antibody problem [J].
Burton, DR ;
Desrosiers, RC ;
Doms, RW ;
Koff, WC ;
Kwong, PD ;
Moore, JP ;
Nabel, GJ ;
Sodroski, J ;
Wilson, IA ;
Wyatt, RT .
NATURE IMMUNOLOGY, 2004, 5 (03) :233-236
[7]   Core structure of gp41 from the HIV envelope glycoprotein [J].
Chan, DC ;
Fass, D ;
Berger, JM ;
Kim, PS .
CELL, 1997, 89 (02) :263-273
[8]   Recent observations on HIV type-1 infection in the genital tract of men and women [J].
Coombs, RW ;
Reichelderfer, PS ;
Landay, AL .
AIDS, 2003, 17 (04) :455-480
[9]   Regulatory challenges in microbicide development [J].
Coplan, PM ;
Mitchnick, M ;
Rosenberg, ZF .
SCIENCE, 2004, 304 (5679) :1911-1912
[10]   Dawn of non-nucleoside inhibitor-based anti-HIV microbicides [J].
D'Cruz, OJ ;
Uckun, FM .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2006, 57 (03) :411-423