4.0 Article

Increased Cervical CD4+CCR5+ T Cells Among Kenyan Sex Working Women Using Depot Medroxyprogesterone Acetate

期刊

AIDS RESEARCH AND HUMAN RETROVIRUSES
卷 35, 期 3, 页码 236-246

出版社

MARY ANN LIEBERT, INC
DOI: 10.1089/aid.2018.0188

关键词

depot medroxyprogesterone acetate (DMPA); HIV target cells; immune activation; ectocervix; cervical biopsy; contraception

资金

  1. Canadian Institutes of Health Research (CIHR) [86721]
  2. Swedish Research Council
  3. CIHR
  4. Fond de la recherche-Sante (FRQ-S)
  5. University of Manitoba's CIHR International Infectious Diseases and Global Health Training Program

向作者/读者索取更多资源

Depot medroxyprogesterone acetate (DMPA) is the most common hormonal contraceptive used by women in sub-Saharan Africa, however, it has been epidemiologically associated with HIV infections. To assess whether DMPA has an effect on the number and activation of HIV target cells, this study assessed the levels and phenotype of blood- and mucosal-derived HIV target cells among women using DMPA. Thirty-five HIV uninfected women from the Pumwani Sex Worker cohort from Nairobi, Kenya were enrolled in the study (15 using DMPA and 20 not using hormonal contraception). Blood (plasma and peripheral blood mononuclear cells) and cervicovaginal (lavage, cervical cells, and ectocervical biopsies) samples were collected. Cellular phenotype and activation status were determined by flow cytometry, cytokine levels were assessed by bead array and image analysis assessed cell number and phenotype in situ. In blood, the proportion of HIV target cells and activated T cells was lower in DMPA users versus those not using hormonal contraceptives. However, analysis of cervical mononuclear cells showed that DMPA users had elevated levels of activated T cells (CD4(+)CD69(+)) and expressed lower levels of the HIV co-receptor CCR5 on a per cell basis, while tissue samples showed that in the ectocervix, DMPA users had a higher proportion of CD4(+)CCR5(+) T cells. This study demonstrates that DMPA users had higher levels of activated T cells and HIV target cells in the genital tract. The increased pool of mucosal HIV target cells provides new biological information about the potential impact of DMPA on HIV susceptibility.

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