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Published on: April 3, 2026
The immune system of preterm infants: an overview
Mirjam J Esser1,2, Sanne J C M Claassen2,3, Melania P Ebrahimi1
1Department of Pediatrics, Maastricht University Medical Center, MosaKids Children's Hospital, Maastricht, Netherlands.
Insights
Preterm infants have immature immune systems, increasing infection risks. Their immune function rapidly matures in the first year, improving but still differing from full-term infants.
Area of Science:
- Immunology
- Neonatal Medicine
- Pediatrics
Background:
- Approximately 13 million infants are born preterm (<37 weeks gestation) annually.
- Preterm infants face higher infection-related morbidity and mortality due to immune system immaturity.
- This immaturity is particularly pronounced in early life, affecting both innate and adaptive immunity.
Purpose of the Study:
- To provide an updated overview of immune system phenotype and function in preterm infants compared to term infants.
- To emphasize the adaptive immunity aspects in preterm infants.
- To offer a framework for understanding the immunological mechanisms behind increased infection risk in preterm infants.
Main Methods:
- This study is a review of current literature.
- It compares the immune system of preterm infants with that of term infants.
- The focus is on phenotypic and functional characteristics, including adaptive immunity.
Main Results:
- Preterm infants exhibit immature innate and adaptive immune cells at birth.
- Reduced antibody levels and diminished vaccine immunogenicity are observed.
- Impaired pathogen clearance and suboptimal vaccine responses contribute to increased susceptibility.
Conclusions:
- Immune immaturity is a significant factor in the heightened infection risk for preterm infants.
- Rapid immune maturation occurs during the first year of life.
- Understanding these immunological mechanisms is crucial for developing strategies to improve preterm infant health outcomes.
Abstract:
Every year, approximately 13 million infants are born preterm (<37 weeks gestation). Preterm-born infants experience disproportionately high infection-related morbidity and mortality, reflecting the immaturity of their immune system, especially early in life. This review provides an up-to-date overview of the phenotype and function of the immune system in preterm infants compared with term infants, with an emphasis on adaptive immunity. At birth, both innate and adaptive immune cells of preterm infants show phenotypic and functional immaturity. In addition, antibody levels are reduced, and immunogenicity of some vaccine components is diminished, contributing to impaired pathogen clearance and suboptimal vaccine responses. During the first year of life, rapid maturation occurs and differences with term infants become less pronounced or disappear. This review provides readers with a framework for understanding the immunologic mechanisms underlying the increased infection risk in preterm-born infants. Recognizing the all-encompassing nature of immune immaturity in preterm infants is essential for the development of integrated strategies to further improve health outcomes.
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