Extended Postexposure Protection Against Vaginal Simian/Human Immunodeficiency Virus Infection With Tenofovir Alafenamide Fumarate/Elvitegravir Inserts in Macaques

被引:2
|
作者
Makarova, Natalia [1 ]
Singletary, Tyana [1 ]
Melissa Peet, M. [2 ]
Mitchell, James [1 ]
Bachman, Shanon [1 ]
Holder, Angela [1 ]
Dinh, Chuong [1 ]
Lipscomb, Jonathan [1 ]
Agrahari, Vivek [2 ]
Mendoza, Maria [3 ]
Pan, Yi [3 ]
Heneine, Walid [1 ]
Clark, Meredith R. [2 ]
Garcia-Lerma, J. Gerardo [1 ,4 ]
Doncel, Gustavo F. [2 ,5 ]
Smith, James M. [1 ]
机构
[1] Natl Ctr HIV Viral Hepatitis STD & TB Prevent, CDCP, Div HIV Prevent, Lab Branch, Atlanta, GA 30329 USA
[2] Eastern Virginia Med Sch, CONRAD, Norfolk, VA USA
[3] Natl Ctr HIV Viral Hepatitis STD & TB Prevent, CDCP, Div HIV Prevent, Quantitat Sci Branch, Atlanta, GA USA
[4] CDCP, Div HIV Prevent, Lab Branch, 1600 Clifton Rd NE, Atlanta, GA 30329 USA
[5] Eastern Virginia Med Sch, CONRAD, 601 Colley Ave, Norfolk, VA 23507 USA
来源
JOURNAL OF INFECTIOUS DISEASES | 2024年 / 229卷 / 06期
关键词
HIV preexposure and postexposure prophylaxis; macaque models; topical PrEP and PEP; tenofovir alafenamide; elvitegravir; PREEXPOSURE PROPHYLAXIS; HIV;
D O I
10.1093/infdis/jiad599
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Vaginal inserts that can be used on demand before or after sex may be a desirable human immunodeficiency virus (HIV) prevention option for women. We recently showed that inserts containing tenofovir alafenamide fumarate (TAF, 20 mg) and elvitegravir (EVG, 16 mg) were highly protective against repeated simian/human immunodeficiency virus (SHIV) vaginal exposures when administered to macaques 4 hours before or after virus exposure (93% and 100%, respectively). Here, we show in the same macaque model that insert application 8 hours or 24 hours after exposure maintains high efficacy (94.4% and 77.2%, respectively). These data extend the protective window by TAF/EVG inserts and inform their clinical development for on-demand prophylaxis in women. Vaginal tenofovir alafenamide fumarate/elvitegravir (TAF/EVG) inserts demonstrated efficacy of 94.4% when applied 8 hours after SHIV exposure, but 77.2% when applied at 24 hours. These findings inform further clinical development and trial design of TAF/EVG inserts as a flexible on-demand product for women.
引用
收藏
页码:1791 / 1795
页数:5
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