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慢性鼻-鼻窦炎患者的补体缺陷。

Complement defects in patients with chronic rhinosinusitis.

机构信息

Department of Otorhinolaryngology, Odense University Hospital, Odense, Denmark.

出版信息

PLoS One. 2012;7(11):e47383. doi: 10.1371/journal.pone.0047383. Epub 2012 Nov 7.

Abstract

The complement system is an important part of our immune system, and complement defects lead generally to increased susceptibility to infections and autoimmune diseases. We have studied the role of complement activity in relation with chronic rhinosinusitis (CRS), and more specifically studied whether complement defects collectively predispose individuals for CRS or affect CRS severity. The participants comprised 87 CRS patients randomly selected from the general population, and a control group of 150 healthy blood donors. The CRS patients were diagnosed according to the European Position Paper on Rhinosinusitis and nasal Polyps criteria, and severity was evaluated by the Sino-nasal Outcome Test-22. Serum samples were analysed by ELISA for activity of the respective pathways of complement, and subsequently for serum levels of relevant components. We found that the frequency of complement defects was significantly higher among CRS patients than among healthy control subjects. A majority of Mannan-binding lectin deficient CRS patients was observed. The presence of complement defects had no influence on the severity of subjective symptoms. Our studies show that defects in the complement system collectively may play an immunological role related to the development of CRS. However, an association between severity of symptoms and presence of complement defects could not be demonstrated.

摘要

补体系统是我们免疫系统的重要组成部分,补体缺陷通常会导致易感染和自身免疫性疾病。我们研究了补体活性与慢性鼻-鼻窦炎(CRS)的关系,更具体地研究了补体缺陷是否会共同导致个体易患 CRS 或影响 CRS 的严重程度。参与者包括 87 名从普通人群中随机选择的 CRS 患者和 150 名健康献血者组成的对照组。CRS 患者根据欧洲鼻-鼻窦炎和鼻息肉标准的立场文件进行诊断,严重程度通过 Sino-nasal Outcome Test-22 进行评估。通过 ELISA 分析血清样本中补体各途径的活性,以及相关成分的血清水平。我们发现,补体缺陷在 CRS 患者中的频率明显高于健康对照组。观察到大多数甘露聚糖结合凝集素缺乏的 CRS 患者存在缺陷。补体缺陷的存在对主观症状的严重程度没有影响。我们的研究表明,补体系统的缺陷可能共同发挥与 CRS 发展相关的免疫作用。然而,未能证明症状严重程度与补体缺陷之间存在关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed8b/3492390/fc5de6c76143/pone.0047383.g001.jpg

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