Chronic inflammation with increased human immunodeficiency virus (HIV) RNA expression in the vaginal epithelium of HIV-infected Thai women

被引:25
作者
Cohn, MA
Frankel, SS
Rugpao, S
Young, MA
Willett, G
Tovanabutra, S
Khamboonruang, C
VanCott, T
Bhoopat, L
Barrick, S
Fox, C
Quinn, TC
Vahey, M
Nelson, KE
Weissman, D
机构
[1] Univ Penn, Dept Med, Div Infect Dis, Philadelphia, PA 19104 USA
[2] NIAID, Howard Hughes Med Inst, Res Scholars Program, NIH, Bethesda, MD 20892 USA
[3] Walter Reed Army Inst Res, Div Retrovirol, Rockville, MD USA
[4] Henry M Jackson Fdn Adv Mil Med, Rockville, MD USA
[5] Mol Histol Lab, Gaithersburg, MD USA
[6] Johns Hopkins Univ, Div Infect Dis, Baltimore, MD USA
[7] Johns Hopkins Univ, Sch Hyg & Publ Hlth, Baltimore, MD USA
[8] Georgetown Univ, Dept Infect Dis, Washington, DC USA
[9] Georgetown Univ, Dept Obstet & Gynecol, Washington, DC USA
[10] Armed Forces Inst Pathol, Dept Infect & Parasit Dis Pathol, Washington, DC 20306 USA
[11] Chiang Mai Univ, Res Inst Hlth Sci, Chiang Mai 50000, Thailand
关键词
D O I
10.1086/322780
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Thai residents have a greater risk of heterosexual transmission of human immunodeficiency virus (HIV) than do US residents. To analyze host factors associated with heterosexual transmission, vaginal epithelial biopsies from HIV-seropositive Thai and US women were evaluated for tissue virus load and histologic makeup. In all, 84% of Thai and 14% of US women exhibited a chronic inflammatory T cell infiltrate in the vaginal epithelium. In Thai tissue, the infiltrate was associated with elevated levels of HIV RNA in the epidermis. Uninfected Thai women also had vaginal epithelial inflammation. Inflammation did not correlate with sexually transmitted diseases or HIV disease stage. The higher rates and increased risk of heterosexual transmission in Thailand may be due to chronic inflammation at the site where the virus is transmitted, which leads to the accumulation of activated T cells. Such cells might act as targets for initial viral infection and subsequently as reservoirs that support efficient transmission.
引用
收藏
页码:410 / 417
页数:8
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