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Early Microbial-Immune Interactions and Innate Immune Training of the Respiratory System During Health and Disease

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Specialty Health Services
Date 2021 Jun 2
PMID 34069319
Citations 9
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Abstract

Over the past two decades, several studies have positioned early-life microbial exposure as a key factor for protection or susceptibility to respiratory diseases. Birth cohorts have identified a strong link between neonatal bacterial colonization of the nasal airway and gut with the risk for respiratory infections and childhood asthma. Translational studies have provided companion mechanistic insights on how viral and bacterial exposures in early life affect immune development at the respiratory mucosal barrier. In this review, we summarize and discuss our current understanding of how early microbial-immune interactions occur during infancy, with a particular focus on the emergent paradigm of "innate immune training". Future human-based studies including newborns and infants are needed to inform the timing and key pathways implicated in the development, maturation, and innate training of the airway immune response, and how early microbiota and virus exposures modulate these processes in the respiratory system during health and disease.

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References
1.
Toivonen L, Karppinen S, Schuez-Havupalo L, Waris M, He Q, Hoffman K . Longitudinal Changes in Early Nasal Microbiota and the Risk of Childhood Asthma. Pediatrics. 2020; 146(4). DOI: 10.1542/peds.2020-0421. View

2.
Bisgaard H, Hermansen M, Bonnelykke K, Stokholm J, Baty F, Skytt N . Association of bacteria and viruses with wheezy episodes in young children: prospective birth cohort study. BMJ. 2010; 341:c4978. PMC: 2950260. DOI: 10.1136/bmj.c4978. View

3.
Bisgaard H, Hermansen M, Buchvald F, Loland L, Halkjaer L, Bonnelykke K . Childhood asthma after bacterial colonization of the airway in neonates. N Engl J Med. 2007; 357(15):1487-95. DOI: 10.1056/NEJMoa052632. View

4.
Martinez F . Childhood Asthma Inception and Progression: Role of Microbial Exposures, Susceptibility to Viruses and Early Allergic Sensitization. Immunol Allergy Clin North Am. 2019; 39(2):141-150. PMC: 6613822. DOI: 10.1016/j.iac.2018.12.001. View

5.
Levan S, Stamnes K, Lin D, Panzer A, Fukui E, McCauley K . Elevated faecal 12,13-diHOME concentration in neonates at high risk for asthma is produced by gut bacteria and impedes immune tolerance. Nat Microbiol. 2019; 4(11):1851-1861. PMC: 6830510. DOI: 10.1038/s41564-019-0498-2. View