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A Novel Method for Involving Women of Color at High Risk for Preterm Birth in Research Priority Setting
Published on: January 12, 2018
Why are preterm newborns at increased risk of infection?
Amélie Collins1, Jörn-Hendrik Weitkamp2, James L Wynn3,4
1Division of Neonatology, Department of Pediatrics, Columbia University, New York City, New York, USA.
Insights
Preterm infants face a high risk of infection and sepsis due to unique immune system functions. Understanding these differences is crucial for reducing morbidity and mortality in premature newborns.
Area of Science:
- Neonatal immunology
- Infectious diseases in newborns
Background:
- Premature birth affects 1 in 10 newborns, posing significant health risks.
- Infection and sepsis are major clinical challenges in preterm infants, leading to high morbidity and mortality.
- Preterm infants are disproportionately susceptible to infections compared to other age groups.
Purpose of the Study:
- To review key aspects of innate and adaptive immune function in preterm neonates.
- To elucidate how immune system characteristics contribute to infection and sepsis risk in premature infants.
- To discuss factors influencing sepsis-associated morbidity and mortality in this vulnerable population.
Main Methods:
- Literature review focusing on neonatal immune responses.
- Analysis of immune system development and function in preterm infants.
- Synthesis of current understanding of infection pathogenesis in premature neonates.
Main Results:
- Preterm infants possess a distinct, not merely deficient, immune system.
- Specific aspects of innate and adaptive immunity in preterm neonates increase susceptibility to infections.
- Immune dysregulation contributes significantly to the risk of sepsis and its complications.
Conclusions:
- The unique immune profile of preterm infants is a primary driver of their increased susceptibility to infections and sepsis.
- Targeted research into preterm immunology is essential for developing effective preventative and therapeutic strategies.
- Addressing immune system vulnerabilities can mitigate sepsis-associated morbidity and mortality in premature infants.
Abstract:
One in 10 newborns will be born before completion of 36 weeks' gestation (premature birth). Infection and sepsis in preterm infants remain a significant clinical problem that represents a substantial financial burden on the healthcare system. Many factors predispose premature infants for having the greatest risk of developing and succumbing to infection as compared with all other age groups across the age spectrum. It is clear that the immune system of preterm infants exhibits distinct, rather than simply deficient, function as compared with more mature and older humans and that the immune function in preterm infants contributes to infection risk. While no single review can cover all aspects of immune function in this population, we will discuss key aspects of preterm neonatal innate and adaptive immune function that place them at high risk for developing infections and sepsis, as well as sepsis-associated morbidity and mortality.
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