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Phenotype and Susceptibility to HIV-infection of CD4(+) Th17 Cells in the Human Female Reproductive Tract

Prevention of sexual acquisition of HIV in women requires a substantial increase in our knowledge about HIV-target cell availability and regulation in the female reproductive tract (FRT). In this study, we analyzed the phenotype and susceptibility to HIV-infection of CD4(+) T cell in the endometrium...

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Detalles Bibliográficos
Autores principales: Rodriguez-Garcia, Marta, Barr, Fiona D., Crist, Sarah G., Fahey, John V., Wira, Charles R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4205172/
https://www.ncbi.nlm.nih.gov/pubmed/24759207
http://dx.doi.org/10.1038/mi.2014.26
Descripción
Sumario:Prevention of sexual acquisition of HIV in women requires a substantial increase in our knowledge about HIV-target cell availability and regulation in the female reproductive tract (FRT). In this study, we analyzed the phenotype and susceptibility to HIV-infection of CD4(+) T cell in the endometrium (EM), endocervix (END) and ectocervix (ECT) of the FRT. We found that Th17 cells represent a major subset in FRT tissues analyzed, and that Th17 cells were the main CD4(+) T cell population expressing CCR5 and CD90. In pre-menopausal women, CD4(+) T cells and Th17 cells in particular, were significantly lower in EM relative to END and ECT. Th17 cells were elevated in EM from post-menopausal women relative to pre-menopausal tissues, but not changed in END and ECT. Susceptibility of CD4(+) T cells to HIV infection measured as intracellular p24 was lowest in the EM and highest in ECT. Additionally, we found that Th17 cells co-expressing CCR5 and CD90 were the most susceptible to HIV-infection. Our results provide valuable information for designing preventive strategies directed at targeting highly susceptible target cells in the FRT.