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Effects of the levonorgestrel‐releasing intrauterine device on the immune microenvironment of the human cervix and endometrium

PROBLEM: There is little information regarding the impact of the intrauterine device on immune parameters of the upper female reproductive tract related to risk of HIV acquisition. METHOD OF STUDY: We collected cervical and endometrial samples from women using the hormonal intrauterine device to stu...

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Detalles Bibliográficos
Autores principales: Shanmugasundaram, Uma, Hilton, Joan F., Critchfield, J. William, Greenblatt, Ruth M., Giudice, Linda C., Averbach, Sarah, Seidman, Dominika, Shacklett, Barbara L., Smith‐McCune, Karen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5316474/
https://www.ncbi.nlm.nih.gov/pubmed/27401588
http://dx.doi.org/10.1111/aji.12535
Descripción
Sumario:PROBLEM: There is little information regarding the impact of the intrauterine device on immune parameters of the upper female reproductive tract related to risk of HIV acquisition. METHOD OF STUDY: We collected cervical and endometrial samples from women using the hormonal intrauterine device to study its effects on endocervical cytokines/chemokine concentrations, phenotypic markers of T cells, responses of endometrial T cells to activation, and alterations of endometrial cellular infiltrates. RESULTS: Hormonal intrauterine device use was associated with: increased concentrations of inflammatory cytokines/chemokines (endocervix); increased coexpression of CXCR4 and CCR5 (endocervix and endometrium); increased coexpression of CD38 and HLADR (endocervix and endometrium); increased intracellular IL‐10 production after T‐cell stimulation (endometrium); and increased density of T cells, most notably regulatory T cells (endometrium). CONCLUSION: Hormonal intrauterine device use resulted in both inflammatory and immunosuppressive alterations. Further research is needed to determine the significance of these changes for HIV risk.