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表面活性蛋白 A:哮喘的先天免疫调节剂和治疗靶点。

SURFACTANT PROTEIN A: AN INNATE IMMUNE MODULATOR AND THERAPEUTIC IN ASTHMA.

机构信息

New York, New York.

出版信息

Trans Am Clin Climatol Assoc. 2024;134:94-112.

Abstract

Surfactant Protein A (SP-A) is an innate immune modulator produced by the lung with known protective effects against bacteria and viruses. Its role in asthma, an inflammatory lung disease that affects 10% of the world's population, is not entirely known. In this review, we demonstrate that SP-A confers protection against exposure to interleukin-13, a type 2 cytokine integral to eosinophilic asthma, in a mouse model of SP-A deficiency, a house dust mite model of asthma, and in human bronchial epithelial cells from participants with asthma. We also show that small peptides derived from SP-A, such as the major allele of single nucleotide polymorphism (SNP) rs1965708, which includes the carbohydrate recognition domain of SP-A2 at position 223, reduce airway hyperresponsiveness, airway eosinophils, and mucus in a mouse model of asthma. These data suggest that SP-A has beneficial effects relevant to asthma and that an SP-A peptide may have a new therapeutic use in asthma.

摘要

表面活性蛋白 A(SP-A)是一种由肺部产生的先天免疫调节剂,具有对抗细菌和病毒的已知保护作用。其在哮喘(一种影响全球 10%人口的炎症性肺部疾病)中的作用尚不完全清楚。在这篇综述中,我们证明了 SP-A 在 SP-A 缺乏症的小鼠模型、尘螨诱导的哮喘模型和哮喘患者的人支气管上皮细胞中,对白细胞介素 13(一种与嗜酸性粒细胞性哮喘密切相关的 2 型细胞因子)的暴露具有保护作用。我们还表明,源自 SP-A 的小肽,如单核苷酸多态性(SNP)rs1965708 的主要等位基因,其中包括 SP-A2 第 223 位的碳水化合物识别结构域,可减少哮喘小鼠的气道高反应性、气道嗜酸性粒细胞和黏液。这些数据表明 SP-A 对哮喘具有有益作用,并且 SP-A 肽可能在哮喘的治疗中有新的用途。

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