4.7 Article

Role of S100A9 in the development of neutrophilic inflammation in asthmatics and in a murine model

Journal

CLINICAL IMMUNOLOGY
Volume 183, Issue -, Pages 158-166

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.clim.2017.08.013

Keywords

Calgranulin B; S100A9; Asthma; IL-113; IL-17; IFN-gamma

Categories

Funding

  1. National Research Foundation of Korea [2017R1A2B4012693]
  2. Soonchunhyang University
  3. National Research Foundation of Korea [2017R1A2B4012693] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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S100A9 is an endogenous danger signal that promotes and exacerbates the neutrophilic inflammatory response. To investigate the role of S100A9 in neutrophilic asthma, S100A9 levels were measured in sputum from 101 steroid-naive asthmatics using an ELISA kit and the levels were significantly correlated with percentages of neutrophils in sputum. Intranasal administration of recombinant S100A9 markedly increased neutrophil numbers at 8 h and 24 h later with concomitant elevation of 1L-1 beta, IL-17, and IFN-gamma levels. Treatment with an anti-S100A9 antibody restored the increased numbers of neutrophils and the increased airway resistance in OVA/CFA mice toward the levels of sham-treated mice. Concomitantly, the S100A9 and neutrophil elastase double positive cells were markedly reduced with attenuation of IL-1 beta IL-17, and IFN-gamma levels by the treatment with the antiS100A9 antibody. Our data support a role of S100A9 to initiate and amplify the neutrophilic inflammation in asthma, possibly via inducing IL-1 beta, IL-17 and IFN-gamma. (C) 2017 Elsevier Inc. All rights reserved.

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