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Immunization of pregnant women: Future of early infant protection

Journal

HUMAN VACCINES & IMMUNOTHERAPEUTICS
Volume 11, Issue 11, Pages 2549-2555

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/21645515.2015.1070984

Keywords

antibody; B cell; clinical trial; immunization; infection; mucosal immunity; neonatal Fc receptor; pregnancy; vaccine; vaccine safety

Funding

  1. Wayne State University OVPR
  2. American Congress of Obstetricians and Gynecologists Industrial Award on Immunization
  3. Burroughs Wellcome Fund Preterm Birth Initiative
  4. National Institutes of Health [U01AI95776]
  5. Wayne State University Maternal Perinatal and Child Health Initiative
  6. Wayne State University Office of the Vice President for Research (OVPR)
  7. Barbara Ann Karmanos Cancer Institute

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Children in early infancy do not mount effective antibody responses to many vaccines against commons infectious pathogens, which results in a window of increased susceptibility or severity infections. In addition, vaccine-preventable infections are among the leading causes of morbidity in pregnant women. Immunization during pregnancy can generate maternal immune protection as well as elicit the production and transfer of antibodies cross the placenta and via breastfeeding to provide early infant protection. Several successful vaccines are now recommended to all pregnant women worldwide. However, significant gaps exist in our understanding of the efficacy and safety of other vaccines and in women with conditions associated with increased susceptible to high-risk pregnancies. Public acceptance of maternal immunization remained to be improved. Broader success of maternal immunization will rely on the integration of advances in basic science in vaccine design and evaluation and carefully planned clinical trials that are inclusive to pregnant women.

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