过敏和耐受诱导中的T细胞亚群。

IF 4.5 3区 医学 Q2 IMMUNOLOGY
Ina Suhrkamp, Alexander Scheffold, Guido Heine
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引用次数: 0

摘要

抗原特异性T淋巴细胞是对无害抗原的耐受性和免疫病理的中心调节因子,也是抗原特异性免疫治疗的关键靶点。近年来,通过多参数流式细胞术或单细胞测序直接表征过敏原特异性T细胞的技术得到了改进,从而使人们对耐受性和过敏性T细胞的理解取得了进展。这解开了表型和功能不同的群体,如2a型辅助T细胞(Th2a)、滤泡性Th细胞(Tfh)、调节性T细胞(Treg)、1型调节性T淋巴细胞(Tr1)和滤泡性T调节细胞。在这里,我们将讨论不同Th细胞亚群在健康状态下、过敏的致敏和发展过程中以及过敏原免疫疗法(AIT)诱导耐受中的作用。迄今为止,AIT作为过敏的唯一因果治疗方法的机制尚不完全清楚。在AIT过程中直接离体分析过敏原特异性T细胞支持特异性Th2(a)细胞缺失的概念,而不是作为潜在机制的过敏原特异性Tr1或Treg细胞的扩增。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

T-cell subsets in allergy and tolerance induction

T-cell subsets in allergy and tolerance induction

Antigen-specific T lymphocytes are the central regulators of tolerance versus immune pathology against otherwise innocuous antigens and key targets of antigen-specific immune therapy. Recent advances in the understanding of T cells in tolerance and allergy resulted from improved technologies to directly characterize allergen-specific T cells by multiparameter flow cytometry or single-cell sequencing. This unravelled phenotypically and functionally distinct populations, such as Type 2a T helper cells (Th2a), follicular Th cells (Tfh), regulatory T cells (Treg), Type 1 regulatory T cells (Tr1), and follicular T regulatory cells. Here we will discuss the role of the different Th-cell subsets in the healthy state, during sensitization and development of allergy, and in tolerance induction by allergen immunotherapy (AIT). To date, the mechanisms of AIT as the only causal treatment of allergy are not completely understood. The analyses of allergen-specific T cells directly ex vivo during AIT support the concept of specific-Th2(a) cell deletion rather than an expansion of allergen-specific Tr1 or Treg cells as underlying mechanism.

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来源期刊
CiteScore
8.30
自引率
3.70%
发文量
224
审稿时长
2 months
期刊介绍: The European Journal of Immunology (EJI) is an official journal of EFIS. Established in 1971, EJI continues to serve the needs of the global immunology community covering basic, translational and clinical research, ranging from adaptive and innate immunity through to vaccines and immunotherapy, cancer, autoimmunity, allergy and more. Mechanistic insights and thought-provoking immunological findings are of interest, as are studies using the latest omics technologies. We offer fast track review for competitive situations, including recently scooped papers, format free submission, transparent and fair peer review and more as detailed in our policies.
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