The adaptive immune system in early life: The shift makes it count

Respiratory infectious diseases encountered early in life may result in life-threatening disease in neonates, which is primarily explained by the relatively naive neonatal immune system. Whereas vaccines are not readily available for all infectious diseases, vaccinations have greatly reduced childho...

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Published inFrontiers in immunology Vol. 13; p. 1031924
Main Authors Pieren, Daan K. J., Boer, Mardi C., de Wit, Jelle
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 17.11.2022
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Summary:Respiratory infectious diseases encountered early in life may result in life-threatening disease in neonates, which is primarily explained by the relatively naive neonatal immune system. Whereas vaccines are not readily available for all infectious diseases, vaccinations have greatly reduced childhood mortality. However, repeated vaccinations are required to reach protective immunity in infants and not all vaccinations are effective at young age. Moreover, protective adaptive immunity elicited by vaccination wanes more rapidly at young age compared to adulthood. The infant adaptive immune system has previously been considered immature but this paradigm has changed during the past years. Recent evidence shows that the early life adaptive immune system is equipped with a strong innate-like effector function to eliminate acute pathogenic threats. These strong innate-like effector capacities are in turn kept in check by a tolerogenic counterpart of the adaptive system that may have evolved to maintain balance and to reduce collateral damage. In this review, we provide insight into these aspects of the early life’s adaptive immune system by addressing recent literature. Moreover, we speculate that this shift from innate-like and tolerogenic adaptive immune features towards formation of immune memory may underlie different efficacy of infant vaccination in these different phases of immune development. Therefore, presence of innate-like and tolerogenic features of the adaptive immune system may be used as a biomarker to improve vaccination strategies against respiratory and other infections in early life.
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Present address: Daan K. J. Pieren, Infectious Diseases Department, Vall d’Hebron Research Institute (VHIR), Vall d’Hebron Hospital Universitari, Barcelona, Spain
Edited by: Kerry M. Empey, University of Pittsburgh, United States
Reviewed by: Erguang Li, Nanjing University, China; Sergej Tomić, Institute for the Application of Nuclear Energy (INEP), Serbia; Urban Švajger, Blood Transfusion Centre of Slovenia, Slovenia
This article was submitted to Vaccines and Molecular Therapeutics, a section of the journal Frontiers in Immunology
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2022.1031924