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    Toll-like receptor induced pro-interleukin-1beta and interleukin-6 in monocytes are lower in healthy infants compared to adults

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    Authors
    Libraty, Daniel H.
    Zhang, Lei
    Woda, Marcia
    Acosta, Luz P.
    Obcena, Anamae
    Brion, Job D.
    Capeding, Rosario Z.
    UMass Chan Affiliations
    Department of Medicine, Division of Infectious Diseases and Immunology
    Document Type
    Journal Article
    Publication Date
    2013-10-25
    Keywords
    Immunity
    Immunology of Infectious Disease
    
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    Abstract
    Infants have long been known to have higher infectious diseases morbidity and mortality and suboptimal vaccination responses compared to older children and adults. A variety of differences in innate and adaptive immune responses have been described between these two groups. We compared Toll-like receptor (TLR)-induced production of pro-interleukin (IL)-1beta, IL-6, and tumor necrosis factor (TNF)-alpha between 2-month-old infants and adults. TLR 7/8-induced production of pro-IL-1beta and IL-6 in monocytes was lower in 2-month-old infants compared to adults. There was no difference in TLR 7/8-induced production of TNF-alpha. Lower TLR-induced production of pro-IL-1beta and IL-6 in innate immune cells during early infancy likely contributes to suboptimal vaccine responses and infectious diseases susceptibility.
    Source
    Libraty DH, Zhang L, Woda M, Acosta LP, Obcena A, et al. (2013) Toll-Like Receptor Induced Pro-Interleukin-1β and Interleukin-6 in Monocytes Are Lower in Healthy Infants Compared to Adults. PLoS ONE 8(10): e78018. doi:10.1371/journal.pone.0078018 Link to article on publisher's site
    DOI
    10.1371/journal.pone.0078018
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/39611
    PubMed ID
    24205068
    Related Resources
    Link to Article in PubMed
    Rights

    Copyright 2013 Libraty et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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    10.1371/journal.pone.0078018
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