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S100A9在哮喘患者及小鼠模型嗜中性粒细胞炎症发展中的作用。

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

作者信息

Lee Tae-Hyeong, Chang Hun Soo, Bae Da-Jeong, Song Hyun Ji, Kim Myung-Sin, Park Jong Sook, Jun Ji Ae, Lee Si Young, Uh Soo Taek, Kim Soo Hyun, Park Choon-Sik

机构信息

Department of Interdisciplinary Program in Biomedical Science Major, Soonchunhyang Graduate School, Bucheon, Gyeonggi-do 420-767, Republic of Korea.

Department of Internal Medicine, Soonchunhyang University Gumi Hospital, Gumi, Gyeongsangbuk-do 39371, Republic of Korea.

出版信息

Clin Immunol. 2017 Oct;183:158-166. doi: 10.1016/j.clim.2017.08.013. Epub 2017 Aug 25.

DOI:10.1016/j.clim.2017.08.013
PMID:28847516
Abstract

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-naïve 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 8h and 24h later with concomitant elevation of IL-1β, IL-17, and IFN-γ 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-1β, IL-17, and IFN-γ levels by the treatment with the anti-S100A9 antibody. Our data support a role of S100A9 to initiate and amplify the neutrophilic inflammation in asthma, possibly via inducing IL-1β, IL-17 and IFN-γ.

摘要

S100A9是一种内源性危险信号,可促进并加剧嗜中性粒细胞炎症反应。为了研究S100A9在嗜中性粒细胞性哮喘中的作用,使用酶联免疫吸附测定试剂盒对101例未使用过类固醇的哮喘患者痰液中的S100A9水平进行了检测,结果发现该水平与痰液中嗜中性粒细胞百分比显著相关。鼻内给予重组S100A9后,8小时和24小时后嗜中性粒细胞数量显著增加,同时白细胞介素-1β(IL-1β)、白细胞介素-17(IL-17)和干扰素-γ(IFN-γ)水平升高。用抗S100A9抗体治疗可使卵清蛋白/完全弗氏佐剂(OVA/CFA)小鼠中增加的嗜中性粒细胞数量和增加的气道阻力恢复到假手术处理小鼠的水平。同时,抗S100A9抗体治疗可使S100A9和嗜中性粒细胞弹性蛋白酶双阳性细胞显著减少,同时IL-1β、IL-17和IFN-γ水平降低。我们的数据支持S100A9可能通过诱导IL-1β、IL-17和IFN-γ来启动和放大哮喘中的嗜中性粒细胞炎症。

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