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在接受或不接受 SIT 的变应性哮喘儿童中诱导 CD4+CD25+Foxp3+IL-10+T 细胞。

Induction of CD4+CD25+Foxp3+IL-10+ T cells in HDM-allergic asthmatic children with or without SIT.

机构信息

Asthma Center, Beijing Children's Hospital, Capital Medical University, 56 South Lishi Road, Beijing, PR China.

出版信息

Int Arch Allergy Immunol. 2010;153(1):19-26. doi: 10.1159/000301575. Epub 2010 Mar 30.

DOI:10.1159/000301575
PMID:20357481
Abstract

BACKGROUND

Regulatory T cells and immunosuppressive cytokines, such as IL-10 and TGF-beta(1), may have a role in clinically effective allergen-specific immunotherapy. IL-10-secreting regulatory T cells have emerged as potential mediators of immune tolerance in numerous murine models of immunopathology. The aim of this study was to evaluate the frequency and function of regulatory T cells in the response to house dust mite (HDM) immunotherapy.

METHODS

PBMCs were isolated from 27 HDM-allergic asthmatic children who underwent immunotherapy for 1.5-2 years (SIT group) and from 27 matched treated asthmatic children allergic to HDM (asthma group). After 48 h of in vitro stimulation with HDM extracts, regulatory T cells were measured by flow cytometry. Production of IL-4, IFN-gamma and TGF-beta(1 )in supernatants from allergen-stimulated cultures and the PBMC proliferations were measured by ELISA. Sera were tested for allergen-specific IgE using the ImmunoCAP 100 assay.

RESULTS

Patients undergoing immunotherapy produced significantly more IL-10 and showed a significant reduction in proliferation induced by HDM extract compared with the asthma group. In cultures stimulated with HDM extract, the amounts of IL-4 and TGF-beta were lower and the amounts of IFN-gamma were higher in the SIT group compared with the asthma group.

CONCLUSION

There is a functional, but quantitative, insufficiency of Treg cells in allergic asthmatic children, which was reversed in SIT-treated children. SIT can up-regulate the function of CD4(+)CD25(+)Foxp3(+) Treg cells.

摘要

背景

调节性 T 细胞和免疫抑制细胞因子,如 IL-10 和 TGF-β(1),可能在临床上有效的过敏原特异性免疫治疗中发挥作用。在许多免疫病理学的鼠模型中,IL-10 分泌的调节性 T 细胞已成为免疫耐受的潜在介质。本研究旨在评估调节性 T 细胞在屋尘螨(HDM)免疫治疗反应中的频率和功能。

方法

从 27 名接受 1.5-2 年免疫治疗的 HDM 过敏哮喘儿童(SIT 组)和 27 名接受 HDM 治疗的过敏哮喘儿童(哮喘组)中分离 PBMC。用 HDM 提取物体外刺激 48 小时后,通过流式细胞术测量调节性 T 细胞。通过 ELISA 测量过敏原刺激培养物上清液中 IL-4、IFN-γ和 TGF-β(1)的产生以及 PBMC 增殖。使用 ImmunoCAP 100 测定法检测血清中的过敏原特异性 IgE。

结果

与哮喘组相比,接受免疫治疗的患者产生了更多的 IL-10,并且对 HDM 提取物诱导的增殖有明显的抑制作用。与哮喘组相比,在 HDM 提取物刺激的培养物中,SIT 组的 IL-4 和 TGF-β 量较低,IFN-γ量较高。

结论

在过敏性哮喘儿童中存在功能但数量不足的 Treg 细胞,在 SIT 治疗的儿童中得到逆转。SIT 可以上调 CD4(+)CD25(+)Foxp3(+)Treg 细胞的功能。

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