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      Risks associated with viral infections during pregnancy

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          Abstract

          Despite the prevalence of viral infections in the American population, we still have a limited understanding of how they affect pregnancy and fetal development. Viruses can gain access to the decidua and placenta by ascending from the lower reproductive tract or via hematogenous transmission. Viral tropism for the decidua and placenta is then dependent on viral entry receptor expression in these tissues as well as on the maternal immune response to the virus. These factors vary by cell type and gestational age and can be affected by changes to the in utero environment and maternal immunity. Some viruses can directly infect the fetus at specific times during gestation, while some only infect the placenta. Both scenarios can result in severe birth defects or pregnancy loss. Systemic maternal viral infections can also affect the pregnancy, and these can be especially dangerous, because pregnant women suffer higher virus-associated morbidity and mortality than do nonpregnant counterparts. In this Review, we discuss the potential contributions of maternal, placental, and fetal viral infection to pregnancy outcome, fetal development, and maternal well-being.

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          Author and article information

          Contributors
          Journal
          J Clin Invest
          J. Clin. Invest
          J Clin Invest
          The Journal of Clinical Investigation
          American Society for Clinical Investigation
          0021-9738
          1558-8238
          1 May 2017
          1 May 2017
          1 May 2018
          : 127
          : 5
          : 1591-1599
          Affiliations
          [1 ]Department of Obstetrics, Gynecology, and Reproductive Biology, College of Human Medicine, Michigan State University, Grand Rapids, Michigan, USA.
          [2 ]Department of Obstetrics, Gynecology, and Reproductive Sciences, Yale School of Medicine, New Haven, Connecticut, USA.
          Author notes
          Address correspondence to: Gil Mor, Department of Obstetrics, Gynecology and Reproductive Sciences, Division of Reproductive Sciences, Yale School of Medicine, 333 Cedar St., LSOG 305A, New Haven, Connecticut 06520, USA. Phone: 203.785.6294; E-mail: gil.mor@ 123456yale.edu .
          Author information
          http://orcid.org/0000-0002-5499-3912
          Article
          PMC5409792 PMC5409792 5409792 87490
          10.1172/JCI87490
          5409792
          28459427
          ec360ccc-9178-4b4c-aa54-fadbc619b173
          Copyright © 2017, American Society for Clinical Investigation
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