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Updated: May 15, 2026

A Neonatal Imaging Model of Gram-Negative Bacterial Sepsis
Published on: August 12, 2020
Role of innate immunity in neonatal infection
Alex G Cuenca1, James L Wynn, Lyle L Moldawer
1Department of Surgery, University of Florida, Gainesville, FL, USA.
Insights
Newborns have a unique immune system making them vulnerable to infections. Research explores enhancing infant immunity with antimicrobial proteins and peptides for better defense.
Area of Science:
- Immunology
- Neonatal Medicine
- Infectious Diseases
Background:
- Newborns face heightened infection risks from genetic, epigenetic, and environmental factors.
- Neonatal innate immune system plays a crucial role in host defense against pathogens.
- Distinct immune profiles in term and preterm newborns influence susceptibility.
Purpose of the Study:
- To examine the neonatal innate immune system's role in defending against bacterial and viral infections.
- To understand the vulnerabilities of newborns to intracellular pathogens and pyogenic bacteria.
- To identify potential strategies for enhancing infant immune responses.
Main Methods:
- Analysis of neonatal innate immune system characteristics.
- Comparison of immune responses in full-term versus preterm newborns.
- Review of ongoing research into immune response modifiers and vaccine adjuvants.
Main Results:
- Full-term newborns exhibit a T(H)2-/T(H)17-biased immune system with impaired T(H)1 responses, increasing vulnerability to intracellular pathogens.
- Preterm newborns show additional deficits including fragile skin, impaired T(H)17 production, and reduced complement and antimicrobial protein/peptide (APP) expression.
- These factors contribute to susceptibility to various infections in newborns.
Conclusions:
- The neonatal immune system's distinct features predispose newborns to specific infections.
- Antimicrobial proteins and peptides (APPs), such as bacterial/permeability-increasing protein and lactoferrin, are key targets for enhancing infant immunity.
- APP-based strategies and pattern recognition receptor agonists show promise as immune response modifiers or vaccine adjuvants for infants.
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 T(H)2-/T(H)17-polarizing and anti-inflammatory cytokine production with relative impairment in T(H)1-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 T(H)17-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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