Am J Perinatol 2013; 30(02): 105-112
DOI: 10.1055/s-0032-1333412
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Role of Innate Immunity in Neonatal Infection

Alex G. Cuenca
1   Department of Surgery, University of Florida, Gainesville, Florida
,
James L. Wynn
2   Division of Neonatology, Department of Pediatrics, Vanderbilt University, Nashville, Tennessee
,
Lyle L. Moldawer
1   Department of Surgery, University of Florida, Gainesville, Florida
,
Ofer Levy
3   Division of Infectious Diseases, Boston Children's Hospital; Boston, Massachusetts
4   Harvard Medical School, Leder Program in Human Biology & Translational Medicine, Boston, Massachusetts
› Author Affiliations
Further Information

Publication History

07 August 2012

14 December 2012

Publication Date:
07 January 2013 (online)

Abstract

Newborns are at increased risk of infection due to genetic, epigenetic, and environmental factors. Herein we examine the roles of the neonatal innate immune system in host defense against bacterial and viral infections. Full-term newborns express a distinct innate immune system biased toward TH2-/TH17-polarizing and anti-inflammatory cytokine production with relative impairment in TH1-polarizing cytokine production that leaves them particularly vulnerable to infection with intracellular pathogens. In addition to these distinct features, preterm newborns also have fragile skin, impaired TH17-polarizing cytokine production, and deficient expression of complement and of antimicrobial proteins and peptides (APPs) that likely contribute to susceptibility to pyogenic bacteria. Ongoing research is identifying APPs, including bacterial/permeability-increasing protein and lactoferrin, as well as pattern recognition receptor agonists that may serve to enhance protective newborn and infant immune responses as stand-alone immune response modifiers or vaccine adjuvants.

 
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