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Altered Expression of IFN-lambda 2 in Allergic Airway Disorders and Identification of Its Cell Origins

机译:改变IFN-Lambda 2在过敏气道疾病中的表达及其细胞起源的鉴定

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摘要

This study investigated the expression levels of interferon-(IFN-)lambda 2 in peripheral blood and tissues. The results showed that the levels of IFN-lambda 2 were elevated by 17.9% and 14.2% in the plasma of allergic rhinitis (AR) and combined rhinitis with asthma (AR + AS), which was positively correlated with the level of tryptase but negatively correlated with the level of IL-10. IFN-lambda 2 was predominately expressed in the CD16+ cells and CD14+ cells in healthy control subjects (HC) but upregulated only in CD8+ cells of AR and in eosinophils of asthma. It was observed that approximately 6.6% and 7.0% dispersed tonsil cells and 5.8% and 0.44% dispersed lung cells are IFN-lambda 2+ mast cells and macrophages. Moreover, tryptase and agonist peptides of PAR-2 induced enhanced IFN-lambda 2 mRNA expression in A549 cells. In conclusion, the elevated levels of IFN-lambda 2 in the plasma of AR and AR + AS indicate that IFN-lambda 2 is likely to contribute to the pathogenesis of allergic airway disorders. The potential origins of the elevated plasma IFN-lambda 2 include mast cells, macrophages, and epithelial cells in tissues, neutrophils, monocytes, CD8+ T cells, and eosinophils in peripheral blood. Development of IFN-lambda 2 related therapy may help to treat or prevent allergic airway disorders.
机译:该研究研究了外周血和组织中干扰素(IFN-)λ2的表达水平。结果表明,IFN-Lambda 2的水平在过敏性鼻炎(AR)的血浆中升高了17.9%和14.2%,以及哮喘(AR + As)的鼻炎,其与胰蛋白酶水平呈正相关,但负面相关与IL-10的水平相关。 IFN-Lambda 2主要在CD16 +细胞和CD14 +细胞中表达健康对策(HC),但仅在AR的CD8 +细胞和哮喘的嗜酸性粒细胞上上调。观察到,约6.6%和7.0%分散的扁桃体细胞和5.8%和0.44%分散的肺细胞是IFN-Lambda 2+肥大细胞和巨噬细胞。此外,PAR-2的胰蛋白酶和激动剂肽在A549细胞中诱导的增强IFN-Lambda 2 mRNA表达。总之,Ar和Ar +血浆中IFN-Lambda 2的升高,表明IFN-Lambda 2可能有助于过敏气道疾病的发病机制。升高的血浆IFN-Lambda 2的潜在来源包括组织中的肥大细胞,巨噬细胞和上皮细胞,中性粒细胞,单核细胞,CD8 + T细胞和外周血中的嗜酸性粒细胞。 IFN-Lambda 2相关疗法的发展可能有助于治疗或预防过敏气道疾病。

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  • 来源
    《Mediators of inflammation》 |2016年第1期|共13页
  • 作者单位

    Liaoning Med Univ Affiliated Hosp 1 Dept ENT Allergy &

    Clin Immunol Res Ctr Jinzhou 121001;

    Liaoning Med Univ Affiliated Hosp 1 Dept ENT Allergy &

    Clin Immunol Res Ctr Jinzhou 121001;

    Shenyang Mil Reg Gen Hosp Dept Resp Med Shenyang 110016 Liaoning Peoples R China;

    Shenyang Mil Reg Gen Hosp Dept Resp Med Shenyang 110016 Liaoning Peoples R China;

    Liaoning Med Univ Affiliated Hosp 1 Dept ENT Allergy &

    Clin Immunol Res Ctr Jinzhou 121001;

    Shantou Univ Coll Med Allergy &

    Inflammat Res Inst Shantou 515031 Peoples R China;

    Shantou Univ Coll Med Allergy &

    Inflammat Res Inst Shantou 515031 Peoples R China;

    Shantou Univ Coll Med Allergy &

    Inflammat Res Inst Shantou 515031 Peoples R China;

    Shantou Univ Coll Med Allergy &

    Inflammat Res Inst Shantou 515031 Peoples R China;

    Liaoning Med Univ Affiliated Hosp 1 Dept ENT Allergy &

    Clin Immunol Res Ctr Jinzhou 121001;

    Liaoning Med Univ Affiliated Hosp 1 Dept ENT Allergy &

    Clin Immunol Res Ctr Jinzhou 121001;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 病理学;
  • 关键词

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