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Making friends: active selection of symbionts and rejection of pathogens by the neonatal immune system

The neonatal immune system is generally viewed as deficient compared to adults, often attributed to its incomplete development. This view is reinforced by the extraordinary sensitivity and susceptibility of neonates to certain pathogens. Examination of the basis for this susceptibility has character...

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Autores principales: Sedney, Colleen J., Harvill, Eric T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10694279/
http://dx.doi.org/10.3389/fimmu.2023.1287518
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author Sedney, Colleen J.
Harvill, Eric T.
author_facet Sedney, Colleen J.
Harvill, Eric T.
author_sort Sedney, Colleen J.
collection PubMed
description The neonatal immune system is generally viewed as deficient compared to adults, often attributed to its incomplete development. This view is reinforced by the extraordinary sensitivity and susceptibility of neonates to certain pathogens. Examination of the basis for this susceptibility has characterized neonatal immunity as skewed strongly toward anti-inflammatory responses, which are interpreted as the lack of full development of the strong inflammatory responses observed in adults. Here we examine the alternative explanation that neonatal immune responses are generally complete in healthy newborns but evolved and adapted to very different functions than adult immunity. Adult immunity is primarily aimed at controlling pathogens that invade the holobiont, with substantial competition and protection conferred by resident microbiota. Rather than simply repelling new invaders, the immediate and critical challenge of the neonatal immune system during the sudden transition from near sterility to microbe-rich world is the assimilation of a complex microbiota to generate a stable and healthy holobiont. This alternative view of the role of the neonatal immune system both explains its strong anti-inflammatory bias and provides a different perspective on its other unique aspects. Here we discuss recent work exploring the initial contact of newborns with microbes and their interactions with neonatal immune responses, contrasting these alternative perspectives. Understanding how the need to rapidly acquire a highly complex and rich microbiota of commensals affects interactions between the neonatal immune system and both commensals and pathogens will allow more targeted and effective collaboration with this system to quickly achieve a more disease-resistant holobiont.
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spelling pubmed-106942792023-12-05 Making friends: active selection of symbionts and rejection of pathogens by the neonatal immune system Sedney, Colleen J. Harvill, Eric T. Front Immunol Immunology The neonatal immune system is generally viewed as deficient compared to adults, often attributed to its incomplete development. This view is reinforced by the extraordinary sensitivity and susceptibility of neonates to certain pathogens. Examination of the basis for this susceptibility has characterized neonatal immunity as skewed strongly toward anti-inflammatory responses, which are interpreted as the lack of full development of the strong inflammatory responses observed in adults. Here we examine the alternative explanation that neonatal immune responses are generally complete in healthy newborns but evolved and adapted to very different functions than adult immunity. Adult immunity is primarily aimed at controlling pathogens that invade the holobiont, with substantial competition and protection conferred by resident microbiota. Rather than simply repelling new invaders, the immediate and critical challenge of the neonatal immune system during the sudden transition from near sterility to microbe-rich world is the assimilation of a complex microbiota to generate a stable and healthy holobiont. This alternative view of the role of the neonatal immune system both explains its strong anti-inflammatory bias and provides a different perspective on its other unique aspects. Here we discuss recent work exploring the initial contact of newborns with microbes and their interactions with neonatal immune responses, contrasting these alternative perspectives. Understanding how the need to rapidly acquire a highly complex and rich microbiota of commensals affects interactions between the neonatal immune system and both commensals and pathogens will allow more targeted and effective collaboration with this system to quickly achieve a more disease-resistant holobiont. Frontiers Media S.A. 2023-11-20 /pmc/articles/PMC10694279/ http://dx.doi.org/10.3389/fimmu.2023.1287518 Text en Copyright © 2023 Sedney and Harvill https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Sedney, Colleen J.
Harvill, Eric T.
Making friends: active selection of symbionts and rejection of pathogens by the neonatal immune system
title Making friends: active selection of symbionts and rejection of pathogens by the neonatal immune system
title_full Making friends: active selection of symbionts and rejection of pathogens by the neonatal immune system
title_fullStr Making friends: active selection of symbionts and rejection of pathogens by the neonatal immune system
title_full_unstemmed Making friends: active selection of symbionts and rejection of pathogens by the neonatal immune system
title_short Making friends: active selection of symbionts and rejection of pathogens by the neonatal immune system
title_sort making friends: active selection of symbionts and rejection of pathogens by the neonatal immune system
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10694279/
http://dx.doi.org/10.3389/fimmu.2023.1287518
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