In vivo identification of Langerhans and related dendritic cells infected with HIV-1 subtype E in vaginal mucosa of asymptomatic patients

被引:34
作者
Bhoopat, L [1 ]
Eiangleng, L
Rugpao, S
Frankel, SS
Weissman, D
Lekawanvijit, S
Petchjom, S
Thorner, P
Bhoopat, T
机构
[1] Chiang Mai Univ, Fac Med, Dept Pathol, Chiang Mai 50200, Thailand
[2] Chiang Mai Univ, Fac Med, Dept Obstet & Gynecol, Chiang Mai 50200, Thailand
[3] Chiang Mai Univ, Fac Med, Dept Forens Med, Chiang Mai 50200, Thailand
[4] Armed Forces Inst Pathol, Dept Infect & Parasit Dis Pathol, Washington, DC 20306 USA
[5] Univ Penn, Div Infect Dis, Philadelphia, PA 19104 USA
[6] Univ Toronto, Hosp Sick Children, Div Pathol, Toronto, ON M5G 1X8, Canada
[7] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
关键词
dendritic cells; double immunostaining; HIV-1; HIV-1 subtype E; Langerhans cells; p24; vaginal mucosa;
D O I
10.1038/modpathol.3880472
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
In Thailand, the predominant HIV subtype is E, rather than Subtype B as in North America and Europe, and the predominant mode of transmission is heterosexual contact. Subtype E has the ability to replicate in vitro in Langerhans cells. We hypothesized that this cell type might constitute a reservoir for the HIV virus in vaginal mucosa of asymptomatic carriers. To examine this hypothesis, we compared vaginal tissue histology in HIV-1-seropositive cases with seronegative cases and determined the immunophenotype of HIV-1-infected cells, their numbers, and their distribution in vaginal mucosa. Vaginal biopsies were performed at four different sites from six asymptomatic HIV-1 Subtype E-infected persons and from six seronegative cases at necropsy and examined histologically. Immunophenotyping was performed using immunoperoxidase for Gag p24 HIV, CD3, CD20, CD68, CD1a, S-100 and p55 antigens and by double labeling, combining immunoperoxidase with alkaline phosphatase using pairs of the above antigens. Twenty of twenty-four vaginal biopsies (83.3%) from HIV-seropositive cases showed definite inflammation compared to five of twenty-four vaginal necropsies (20.8%) from HIV-seronegative cases. One third of HIV-seropositive biopsies (8/24) demonstrated p24-positive cells in the epithelium, whereas three-fourths (18/24) of the biopsies revealed p24-positive cells in the lamina propria. All seropositive patients showed positive cells in at least one biopsy, but not all biopsies contained positive cells. Infected cells were more frequently observed at sites of greater inflammation. The dendritic cell count in HIV-seropositive vaginal epithelium was significantly higher than that observed in the seronegative cases (P =.004). The majority of p24-positive cells in the vaginal epithelium were Langerhans cells (CD1a+/ S-100+), whereas in the lamina propria, about half of p24-positive cells were Langerhans-related dendritic cells (p55+ and S-100+) and half were T lymphocytes. In conclusion, the increased propensity for heterosexual transmission of Subtype E may be related to vaginal inflammation, leading to the accumulation of Langerhans cells and related dendritic cells which, once infected with HIV, can act as a reservoir for further virus transmission.
引用
收藏
页码:1263 / 1269
页数:7
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