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Unique alterations in infection‐induced immune activation during pregnancy
Author(s) -
Witkin SS,
Linhares IM,
Bongiovanni AM,
Herway C,
Skupski D
Publication year - 2011
Publication title -
bjog: an international journal of obstetrics and gynaecology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.157
H-Index - 164
eISSN - 1471-0528
pISSN - 1470-0328
DOI - 10.1111/j.1471-0528.2010.02773.x
Subject(s) - immune system , immunology , immunity , fetus , inflammation , amniotic fluid , cytokine , biology , tumor necrosis factor alpha , pregnancy , genetics
Please cite this paper as: Witkin S, Linhares I, Bongiovanni A, Herway C, Skupski D. Unique alterations in infection‐induced immune activation during pregnancy. BJOG 2011;118:145–153. Background Immune responses to infection are uniquely regulated during gestation to allow for antimicrobial defence and tissue repair, whilst preventing damage to developing fetal organs or the triggering of preterm labour. Objective A review and analysis of studies delineating gestation‐specific immune modulation and intra‐amniotic regulation of pro‐inflammatory immunity. Search strategy Identification of the alterations between the fetus/neonate and adult with regard to the endogenous and infection‐induced expression of molecules with immune regulatory properties, and the characterisation of intra‐amniotic immune mediators that inhibit bacterial‐induced pro‐inflammatory cytokine production. Selection criteria English and non‐English publications from 1985 to the present. Data collection and analysis An electronic literature search using MEDLINE, PubMed, articles cited in the primary sources, as well as pregnancy‐related immunology research from our laboratory at Weill Medical College of Cornell University. Main results During fetal development, interleukin (IL)‐23, IL‐10 and IL‐6, as well as T‐helper‐17 (Th17)‐mediated immune responses, are upregulated, whereas tumour necrosis factor‐α (TNF‐α) and IL‐1β‐ and Th1‐mediated immune responses are downregulated in the intrauterine environment (both the fetal compartment and the amniotic compartment). Infection‐related immunity during gestation is preferentially directed towards combating extracellular microbial pathogens. Amniotic fluid and the neonatal circulation contain multiple components that improve the ability of the developing neonate to tolerate microbial‐induced immune activation. Conclusions The repertoire of immune mechanisms to control infection and inflammation differ between fetal and adult life. The dual mechanisms of resistance to infection and tolerance to infection‐induced immune activation prevent damage to the developing fetus and the triggering of premature labour.