Considerations and development of topical microbicides to inhibit the sexual transmission of HIV

被引:109
作者
Turpin, JA [1 ]
机构
[1] TherImmune Res Corp, Dept Immunol & Infect Dis, Gaithersburg, MD 20797 USA
关键词
AIDS; BufferGel; C31G; cervix; cyanovirin-N; drug discovery; HIVPRO; 2000; STD; topical microbicide; transmission; UC-781; vagina; women;
D O I
10.1517/13543784.11.8.1077
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The increased incidence of HIV/AIDS disease in women aged 15 - 49 years has identified the urgent need for a female-controlled, efficacious and safe vaginal topical microbicide. To meet this challenge, new topical microbicide candidates consisting of molecules or formulations that modify the genital environment (BufferGel(TM), engineered Lactobacillus, over-the-counter lubricants), surfactants (C31D/Savvy(TM) sodium dodecyl sulfate, sodium lauryl sulfate), polyanionic polymers (PRO 2000, beta-cyclodextrin, Carraguard(TM) CAP, D2S, SPL-7013), proteins (cyanovirin-N, monoclonal antibodies, thromspondin-1 peptides, Pokeweed antiviral protein and others), reverse transcription inhibitors (PMPA [Tenofovir(TM)), UC-781, SJ-3366, DABO and thiourea) and other molecules (NCp7-specific virucides, chemokine receptor agonists/ antagonists, WHI-05 and WHI-07) are currently being investigated for activity, safety and efficacy. This review will assess the development of these molecules in the context of cervicovaginal defences and the clinical failure of nonoxynol-9.
引用
收藏
页码:1077 / 1097
页数:21
相关论文
共 262 条
[1]   MUTATIONS OF RNA AND PROTEIN SEQUENCES INVOLVED IN HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 PACKAGING RESULT IN PRODUCTION OF NONINFECTIOUS VIRUS [J].
ALDOVINI, A ;
YOUNG, RA .
JOURNAL OF VIROLOGY, 1990, 64 (05) :1920-1926
[2]  
Anderson DJ, 1998, AIDS RES HUM RETROV, V14, pS43
[3]  
Anderson RA, 2000, J ANDROL, V21, P862
[4]  
Arthur LO, 1998, AIDS RES HUM RETROV, V14, pS311
[5]  
AUSTIN CR, 1975, J REPROD FERTIL, P75
[6]   MECHANISM OF INHIBITORY EFFECT OF DEXTRAN SULFATE AND HEPARIN ON REPLICATION OF HUMAN IMMUNODEFICIENCY VIRUS INVITRO [J].
BABA, M ;
PAUWELS, R ;
BALZARINI, J ;
ARNOUT, J ;
DESMYTER, J ;
DECLERCQ, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (16) :6132-6136
[7]   A small-molecule, nonpeptide CCR5 antagonist with highly potent and selective anti-HIV-1 activity [J].
Baba, M ;
Nishimura, O ;
Kanzaki, N ;
Okamoto, M ;
Sawada, H ;
Iizawa, Y ;
Shiraishi, M ;
Aramaki, Y ;
Okonogi, K ;
Ogawa, Y ;
Meguro, K ;
Fujino, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (10) :5698-5703
[8]   DETECTION OF HIV-1 PROVIRAL DNA IN SPERM FROM HIV-1-INFECTED MEN [J].
BAGASRA, O ;
FARZADEGAN, H ;
SESHAMMA, T ;
OAKES, JW ;
SAAH, A ;
POMERANTZ, RJ .
AIDS, 1994, 8 (12) :1669-1674
[9]   Preclinical studies on thiocarboxanilide UC-781 as a virucidal agent [J].
Balzarini, J ;
Naesens, L ;
Verbeken, E ;
Laga, M ;
Van Damme, L ;
Parniak, M ;
Van Mellaert, L ;
Anné, J ;
De Clercq, E .
AIDS, 1998, 12 (10) :1129-1138
[10]   Antiviral activity of cyclosaligenyl prodrugs of acyclovir, carbovir and abacavir [J].
Balzarini, J ;
Haller-Meier, F ;
De Clercq, E ;
Meier, C .
ANTIVIRAL CHEMISTRY & CHEMOTHERAPY, 2001, 12 (05) :301-306