Type I IFNs in the female reproductive tract: The first line of defense in an ever-changing battleground.
Chlamydia
HIV
Type I IFNs
Zika
female reproductive tract
hormonal regulation
mucosal immunity
Journal
Journal of leukocyte biology
ISSN: 1938-3673
Titre abrégé: J Leukoc Biol
Pays: England
ID NLM: 8405628
Informations de publication
Date de publication:
02 2019
02 2019
Historique:
received:
14
05
2018
revised:
15
10
2018
accepted:
18
10
2018
pubmed:
15
12
2018
medline:
17
10
2019
entrez:
15
12
2018
Statut:
ppublish
Résumé
The primary function of the female reproductive tract (FRT) is to enable successful reproduction, yet the biologic mechanisms required to accomplish this, which include fluctuating sex hormones and tolerance of semen and a semi-allogeneic fetus, can leave this unique mucosal environment susceptible to pathogenic challenge. Consequently, the FRT has evolved specialized innate and adaptive immune responses tailored to protecting itself from infection without compromising reproductive success. A family of innate immune cytokines that has emerged as important regulators of these immune responses is the type I IFNs. Type I IFNs are typically rapidly produced in response to pathogenic stimulation and are capable of sculpting pleotropic biologic effects, including immunomodulation, antiproliferative effects, and inducing antiviral and bactericidal molecules. Here, we review what is currently known about type I IFN-mediated immunity in the FRT in human, primate, and murine models and explore their importance with respect to three highly relevant FRT infections: HIV, Zika, and Chlamydia.
Identifiants
pubmed: 30549324
doi: 10.1002/JLB.MR0318-122RR
doi:
Substances chimiques
Gonadal Steroid Hormones
0
Interferon Type I
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
353-361Subventions
Organisme : Victorian State Government's Operational Infrastructure Support fund
Pays : International
Informations de copyright
©2018 Society for Leukocyte Biology.