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Diminished CD103 (αEβ7) Expression on Resident T Cells from the Female Genital Tract of HIV-Positive Women

BACKGROUND: Tissue resident memory T cells (TrM) provide an enhanced response against infection at mucosal surfaces, yet their function has not been extensively studied in humans, including the female genital tract (FGT). METHODS: Using polychromatic flow cytometry, we studied TrM cells, defined as...

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Detalles Bibliográficos
Autores principales: Moylan, David C., Goepfert, Paul A., Kempf, Mirjam-Colette, Saag, Michael S., Richter, Holly E., Mestecky, Jiri, Sabbaj, Steffanie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pathogens and Immunity 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288734/
https://www.ncbi.nlm.nih.gov/pubmed/28164171
http://dx.doi.org/10.20411/pai.v1i2.166
Descripción
Sumario:BACKGROUND: Tissue resident memory T cells (TrM) provide an enhanced response against infection at mucosal surfaces, yet their function has not been extensively studied in humans, including the female genital tract (FGT). METHODS: Using polychromatic flow cytometry, we studied TrM cells, defined as CD62L-CCR7-CD103(+)CD69(+) CD4(+) and CD8(+) T cells in mucosa-derived T cells from healthy and HIV-positive women. RESULTS: We demonstrate that TrM are present in the FGT of healthy and HIV-positive women. The expression of the mucosal retention receptor, CD103, from HIV-positive women was reduced compared to healthy women and was lowest in women with CD4 counts < 500 cells/mm(3). Furthermore, CD103 expression on mucosa-derived CD8(+) T cells correlated with antigen-specific IFN-γ production by mucosal CD4(+) T cells and was inversely correlated with T-bet from CD8(+)CD103(+) mucosa-derived T cells. CONCLUSIONS: These data suggest that CD4(+) T cells, known to be impaired during HIV-1 infection and necessary for the expression of CD103 in murine models, may play a role in the expression of CD103 on resident T cells from the human FGT.