Gestational tissue inflammatory biomarkers at term labor: Aᅡ systematic review of literature
Parturition at term is characterized by inflammatory overload in both feto-maternal tissues. Despite the large number of individual studies on changes in inflammatory biomarkers linked to labor, a comprehensive profile of them in each of the uterine compartments is not available to better understand...
Saved in:
Published in | American journal of reproductive immunology (1989) Vol. 79; no. 2 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
New Haven
Wiley Subscription Services, Inc
01.02.2018
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Parturition at term is characterized by inflammatory overload in both feto-maternal tissues. Despite the large number of individual studies on changes in inflammatory biomarkers linked to labor, a comprehensive profile of them in each of the uterine compartments is not available to better understand their mechanistic contributions to labor. This systematic review investigated the pro- and anti-inflammatory biomarkers reported in intra-uterine tissues (amnion, chorion, decidua, placenta, and myometrium) at term labor. We conducted a systematic review of studies on pro- and anti-inflammatory biomarkers (mRNA and/or protein) reported in feto-maternal tissues during normal human term labor, published in English (1980-2016), in 3 electronic data bases. From a total of 3712 citations, 172 were included for final review. Each tissue expresses a unique set of biomarkers at the time of term labor, but there is significant overlap between tissues. All tissues had IL-6, IL-8, IL-1[beta], COX-2, PGE-2, TNF-[alpha], and hCAP18 in common at term labor. Common and unique inflammatory biomarkers are expressed in various feto-maternal compartments at term labor. Increase in pro-inflammatory markers in all gestational tissue signifies their harmonious functional role in promoting labor. Anti-inflammatory markers at term labor are hardly reported. |
---|---|
ISSN: | 1046-7408 1600-0897 |
DOI: | 10.1111/aji.12776 |