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Cellular immune responses in amniotic fluid of women with a sonographic short cervix.

Authors :
Galaz J
Romero R
Xu Y
Miller D
Levenson D
Para R
Varrey A
Hsu R
Tong A
Hassan SS
Hsu CD
Gomez-Lopez N
Source :
Journal of perinatal medicine [J Perinat Med] 2020 Sep 25; Vol. 48 (7), pp. 665-676.
Publication Year :
2020

Abstract

Objectives A sonographic short cervix is one of the strongest predictors of preterm delivery. However, the cellular immune composition of amniotic fluid in women with a short cervix has not yet been described. Herein, we determined cellular and soluble immune responses in amniotic fluid from pregnant women with a mid-trimester asymptomatic short cervix. Methods Amniotic fluid samples (n=77) were collected from asymptomatic women with a cervical length between 15 and 25 mm (n=36, short cervix) or ≤15 mm (n=41, severely short cervix) diagnosed by ultrasound. Flow cytometry and multiplex measurement of cytokines/chemokines were performed. Results (1) The cellular immune composition of amniotic fluid did not differ between women with a severely short cervix (≤15 mm) and those with a short cervix 15-25 mm; (2) amniotic fluid concentrations of multiple cytokines/chemokines were higher in women with a severely short cervix (≤15 mm) than in those with a short cervix 15-25 mm; (3) the cellular immune composition of amniotic fluid did not differ between women with a severely short cervix (≤15 mm) who ultimately underwent preterm delivery and those who delivered at term; and (4) amniotic fluid concentrations of IL-2, but not other immune mediators, were increased in women with a severely short cervix (≤15 mm) who ultimately delivered preterm compared to those who delivered at term. Conclusions Women with a severely short cervix (≤15 mm) have increased concentrations of pro-inflammatory mediators in the amniotic cavity; yet, these do not translate to changes in the cellular immune response.

Details

Language :
English
ISSN :
1619-3997
Volume :
48
Issue :
7
Database :
MEDLINE
Journal :
Journal of perinatal medicine
Publication Type :
Academic Journal
Accession number :
32716907
Full Text :
https://doi.org/10.1515/jpm-2020-0037