New Approaches to Making the Microenvironment of the Female Reproductive Tract Hostile to HIV

被引:20
作者
Fahey, John V. [1 ]
Bodwell, Jack E. [1 ]
Hickey, Danica K. [1 ]
Ghosh, Mimi [1 ]
Muia, Maria N. [1 ]
Wira, Charles R. [1 ]
机构
[1] Dartmouth Med Sch, Dept Physiol & Neurobiol, Lebanon, NH 03756 USA
基金
美国国家卫生研究院; 比尔及梅琳达.盖茨基金会;
关键词
Antimicrobials; female reproductive tract; HIV; selective estrogen response modifier; ESTROGEN-RECEPTOR-BETA; LEUKOCYTE PROTEASE INHIBITOR; HEPATOCYTE GROWTH-FACTOR; PROGESTERONE-RECEPTOR; GENITAL-TRACT; NONSTEROIDAL ANTIESTROGENS; HUMAN ENDOMETRIUM; EPITHELIAL-CELLS; SERINE-PROTEASE; CATHEPSIN-B;
D O I
10.1111/j.1600-0897.2010.00949.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
P>The studies presented in this review explore three distinct areas with potential for inhibiting HIV infection in women. Based on emerging information from the physiology, endocrinology and immunology of the female reproductive tract (FRT), we propose unique 'works in progress' for protecting women from HIV. Various aspects of FRT immunity are suppressed by estradiol during the menstrual cycle, making women more susceptible to HIV infection. By engineering commensal Lactobacillus to secrete the anti-HIV molecule Elafin as estradiol levels increase, women could be protected from HIV infection. Selective estrogen response modifiers enhance barrier integrity and enhance secretion of protective anti-HIV molecules. Finally, understanding the interactions and regulation of FRT endogenous antimicrobials, proteases, antiproteases, etc., all of which are under hormonal control, will open new avenues to therapeutic manipulation of the FRT mucosal microenvironment. By seeking new alternatives to preventing HIV infection in women, we may finally disrupt the HIV pandemic.
引用
收藏
页码:334 / 343
页数:10
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