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Front Immunol ; 9: 1033, 2018.
Article in English | MEDLINE | ID: mdl-29881378

ABSTRACT

Estradiol-based therapies predispose women to vaginal infections. Moreover, it has long been known that neutrophils are absent from the vaginal lumen during the ovulatory phase (high estradiol). However, the mechanisms that regulate neutrophil influx to the vagina remain unknown. We investigated the neutrophil transepithelial migration (TEM) into the vaginal lumen. We revealed that estradiol reduces the CD44 and CD47 epithelial expression in the vaginal ectocervix and fornix, which retain neutrophils at the apical epithelium through the estradiol receptor-alpha. In contrast, luteal progesterone increases epithelial expression of CD44 and CD47 to promote neutrophil migration into the vaginal lumen and Candida albicans destruction. Distinctive to vaginal mucosa, neutrophil infiltration is contingent to sex hormones to prevent sperm from neutrophil attack; although it may compromise immunity during ovulation. Thus, sex hormones orchestrate tolerance and immunity in the vaginal lumen by regulating neutrophil TEM.


Subject(s)
Candidiasis, Vulvovaginal/immunology , Estrogen Receptor alpha/genetics , Neutrophil Infiltration , Neutrophils/immunology , Transendothelial and Transepithelial Migration , Vagina/immunology , Animals , CD47 Antigen/genetics , CD47 Antigen/immunology , Candida albicans , Cells, Cultured , Cervix Uteri/immunology , Cervix Uteri/microbiology , Estradiol/pharmacology , Estrogen Receptor alpha/immunology , Female , Gonadal Steroid Hormones/pharmacology , Hyaluronan Receptors/genetics , Hyaluronan Receptors/immunology , Mice , Mice, Inbred BALB C , Mice, Inbred C57BL , Mice, Knockout , Progesterone/pharmacology , Vagina/microbiology
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