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Review
. 2014 Aug;72(2):107-16.
doi: 10.1111/aji.12289. Epub 2014 Jul 4.

Understanding the complexity of the immune system during pregnancy

Affiliations
Review

Understanding the complexity of the immune system during pregnancy

Karen Racicot et al. Am J Reprod Immunol. 2014 Aug.

Abstract

Progress in our understanding of the role of the maternal immune system during healthy pregnancy will help us better understand the role of the immune system in adverse pregnancy outcomes. In this review, we discuss our present understanding of the 'immunity of pregnancy' in the context of the response to cervical and placental infections and how these responses affect both the mother and the fetus. We discuss novel and challenging concepts that help explain the immunological aspects of pregnancy and how the mother and fetus respond to infection.

Keywords: Immune regulation; macrophages; pregnancy; trophoblast.

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Figures

Figure 1
Figure 1
The placenta as an immune regulatory organ. Contrary to non pregnant women (A); the presence of the placenta during pregnancy modifies the immunologic response of the mother to microorganisms. The old model (B) conceives the maternal immune system as the major player in response to the fetus and microorganisms (red arrow). Fetal responses (fetus and placenta) are considered limited. The new integrational model takes in consideration the fetal-placental immune response and the maternal immune system as integrated.
Figure 2
Figure 2
Role of the cervix controlling bacterial migration to the upper reproductive tract. A viral infection of the cervix alters the expression and function of TLRs and Defensins, therefore altering the protective role of the cervix.
Figure 3
Figure 3
Role of the placenta as a modulator of fetal and maternal responses. Inflammation at the placenta has a bi-directional effect. Activates the maternal immune system as well as the fetus by creating an inflammatory environment. The inflammatory response may also influence the development of the fetal immune system with important consequences during post-natal age.

References

    1. Mor G, Cardenas I. The immune system in pregnancy: A unique complexity. Am J Reprod Immunol. 2010;63 - PMC - PubMed
    1. Ng SC, Gilman-Sachs A, Thaker P, Beaman KD, Beer AE, Kwak-Kim J. Expression of intracellular Th1 and Th2 cytokines in women with recurrent spontaneous abortion, implantation failures after IVF/ET or normal pregnancy. Am J Reprod Immunol. 2002;48:77–86. - PubMed
    1. Kwak-Kim JY, Gilman-Sachs A, Kim CE. T helper 1 and 2 immune responses in relationship to pregnancy, nonpregnancy, recurrent spontaneous abortions and infertility of repeated implantation failures. Chemical immunology and allergy. 2005;88:64–79. - PubMed
    1. Goldenberg RL, Culhane JF, Iams JD, Romero R. Epidemiology and causes of preterm birth. Lancet. 2008;371:75–84. - PMC - PubMed
    1. Jamieson DJ, Theiler RN, Rasmussen SA. Emerging infections and pregnancy. Emerg Infect Dis. 2006;12:1638–1643. - PMC - PubMed

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