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变应原诱导的 T 细胞活化在过敏性哮喘和鼻炎中的差异:CD28、ICOS 和 CTLA-4 的作用。

Differences in allergen-induced T cell activation between allergic asthma and rhinitis: Role of CD28, ICOS and CTLA-4.

机构信息

INSERM UMR915, Nantes, F-44000 France.

出版信息

Respir Res. 2011 Feb 28;12(1):25. doi: 10.1186/1465-9921-12-25.

DOI:10.1186/1465-9921-12-25
PMID:21356099
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3051906/
Abstract

BACKGROUND

Th2 cell activation and T regulatory cell (Treg) deficiency are key features of allergy. This applies for asthma and rhinitis. However with a same atopic background, some patients will develop rhinitis and asthma, whereas others will display rhinitis only. Co-receptors are pivotal in determining the type of T cell activation, but their role in allergic asthma and rhinitis has not been explored. Our objective was to assess whether allergen-induced T cell activation differs from allergic rhinitis to allergic rhinitis with asthma, and explore the role of ICOS, CD28 and CTLA-4.

METHODS

T cell co-receptor and cytokine expressions were assessed by flow cytometry in PBMC from 18 house dust mite (HDM) allergic rhinitics (R), 18 HDM allergic rhinitics and asthmatics (AR), 13 non allergic asthmatics (A) and 20 controls, with or without anti-co-receptors antibodies.

RESULTS

In asthmatics (A+AR), a constitutive decrease of CTLA-4+ and of CD4+CD25+Foxp3+ cells was found, with an increase of IFN-γ+ cells. In allergic subjects (R + AR), allergen stimulation induced CD28 together with IL-4 and IL-13, and decreased the proportion of CTLA-4+, IL-10+ and CD4+CD25+Foxp3+ cells. Anti-ICOS and anti-CD28 antibodies blocked allergen-induced IL-4 and IL-13. IL-13 production also involved CTLA-4.

CONCLUSIONS

T cell activation differs between allergic rhinitis and asthma. In asthma, a constitutive, co-receptor independent, Th1 activation and Treg deficiency is found. In allergic rhinitis, an allergen-induced Treg cell deficiency is seen, as well as an ICOS-, CD28- and CTLA-4-dependent Th2 activation. Allergic asthmatics display both characteristics.

摘要

背景

Th2 细胞激活和 T 调节细胞(Treg)缺陷是过敏的关键特征。这适用于哮喘和鼻炎。然而,在具有相同过敏背景的情况下,一些患者会发展为鼻炎和哮喘,而另一些患者则仅表现为鼻炎。共受体在确定 T 细胞激活类型方面起着至关重要的作用,但它们在过敏性哮喘和鼻炎中的作用尚未得到探索。我们的目的是评估过敏原诱导的 T 细胞激活是否与过敏性鼻炎到过敏性鼻炎伴哮喘不同,并探讨 ICOS、CD28 和 CTLA-4 的作用。

方法

通过流式细胞术评估 18 例屋尘螨(HDM)过敏鼻炎(R)、18 例 HDM 过敏鼻炎和哮喘(AR)、13 例非过敏性哮喘(A)和 20 例对照者 PBMC 中的 T 细胞共受体和细胞因子表达,有或没有抗共受体抗体。

结果

在哮喘患者(A+AR)中,发现 CTLA-4+和 CD4+CD25+Foxp3+细胞的组成性减少,同时 IFN-γ+细胞增加。在过敏患者(R+AR)中,过敏原刺激诱导 CD28 与 IL-4 和 IL-13 一起,并降低 CTLA-4+、IL-10+和 CD4+CD25+Foxp3+细胞的比例。抗 ICOS 和抗 CD28 抗体阻断了过敏原诱导的 IL-4 和 IL-13。IL-13 的产生也涉及 CTLA-4。

结论

T 细胞激活在过敏性鼻炎和哮喘之间存在差异。在哮喘中,发现一种组成型、共受体非依赖性 Th1 激活和 Treg 缺陷。在过敏性鼻炎中,发现过敏原诱导的 Treg 细胞缺陷,以及 ICOS、CD28 和 CTLA-4 依赖性 Th2 激活。过敏性哮喘患者同时表现出这两种特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbfc/3051906/17679ff1a205/1465-9921-12-25-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbfc/3051906/3b6fab0f7049/1465-9921-12-25-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbfc/3051906/c763dafe77a3/1465-9921-12-25-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbfc/3051906/17679ff1a205/1465-9921-12-25-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbfc/3051906/3b6fab0f7049/1465-9921-12-25-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbfc/3051906/c763dafe77a3/1465-9921-12-25-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbfc/3051906/17679ff1a205/1465-9921-12-25-3.jpg

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