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Review
. 2017 Aug 11:8:957.
doi: 10.3389/fimmu.2017.00957. eCollection 2017.

Postnatal Innate Immune Development: From Birth to Adulthood

Affiliations
Review

Postnatal Innate Immune Development: From Birth to Adulthood

Anastasia Georgountzou et al. Front Immunol. .

Abstract

It is well established that adaptive immune responses are deficient in early life, contributing to increased mortality and morbidity. The developmental trajectories of different components of innate immunity are only recently being explored. Individual molecules, cells, or pathways of innate recognition and signaling, within different compartments/anatomical sites, demonstrate variable maturation patterns. Despite some discrepancies among published data, valuable information is emerging, showing that the developmental pattern of cytokine responses during early life is age and toll-like receptor specific, and may be modified by genetic and environmental factors. Interestingly, specific environmental exposures have been linked both to innate function modifications and the occurrence of chronic inflammatory disorders, such as respiratory allergies. As these conditions are on the rise, our knowledge on innate immune development and its modulating factors needs to be expanded. Improved understanding of the sequence of events associated with disease onset and persistence will lead toward meaningful interventions. This review describes the state-of-the-art on normal postnatal innate immune ontogeny and highlights research areas that are currently explored or should be further addressed.

Keywords: immune trajectories; immune-related diseases; innate immunity; innate ontogeny; postnatal development.

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Figures

Figure 1
Figure 1
Schematic figure of the postnatal development of the innate immune system. The length of the elongated arrowheads indicates the time point at which full functional capacity is obtained and no further changes apparently occur in basic innate immune components, according to the current literature. Light color is applied to fields that remain insufficiently studied up to now. GIS, gastrointestinal system; RS, respiratory system; SF, soluble factors; TLRs, toll-like receptors; AM, alveolar macrophage; NK, natural killer; APCs, antigen-presenting cells.

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References

    1. Adkins B, Leclerc C, Marshall-Clarke S. Neonatal adaptive immunity comes of age. Nat Rev Immunol (2004) 4(7):553–64.10.1038/nri1394 - DOI - PubMed
    1. Futata EA, Fusaro AE, de Brito CA, Sato MN. The neonatal immune system: immunomodulation of infections in early life. Expert Rev Anti Infect Ther (2012) 10(3):289–98.10.1586/eri.12.9 - DOI - PubMed
    1. Levy O. Innate immunity of the human newborn: distinct cytokine responses to LPS and other toll-like receptor agonists. J Endotoxin Res (2005) 11(2):113–6.10.1179/096805105X37376 - DOI - PubMed
    1. Wynn JL, Levy O. Role of innate host defenses in susceptibility to early-onset neonatal sepsis. Clin Perinatol (2010) 37(2):307–37.10.1016/j.clp.2010.04.001 - DOI - PMC - PubMed
    1. Kollmann TR, Crabtree J, Rein-Weston A, Blimkie D, Thommai F, Wang XY, et al. Neonatal innate TLR-mediated responses are distinct from those of adults. J Immunol (2009) 183(11):7150–60.10.4049/jimmunol.0901481 - DOI - PMC - PubMed