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滤泡性T细胞与IgE反应的调控

Follicular T cells and the control of IgE responses.

作者信息

Cañete Pablo F, Yu Di

机构信息

Frazer Institute, Faculty of Medicine, The University of Queensland, Brisbane, Australia; Ian Frazer Centre for Children's Immunotherapy Research, Child Health Research Centre, Faculty of Medicine, The University of Queensland, Brisbane, Australia.

出版信息

Allergol Int. 2025 Jan;74(1):13-19. doi: 10.1016/j.alit.2024.09.007. Epub 2024 Oct 24.

Abstract

Atopy is considered the epidemic of the 21st century, and while decades of research have established a direct link between Th2 cells driving pathogenic IgE-mediated allergic disease, only in the past years have T follicular helper (Tfh) cells emerged as pivotal drivers of these responses. In this review, we will examine the molecular mechanisms governing the IgE response, with a particular emphasis on the key cytokines and signaling pathways. We will discuss the exclusion of IgE-producing B cells from germinal centers and explore the recently established role of follicular T cell function and heterogeneity in driving or curtailing these immune responses. Additionally, we will assess the current state of major monoclonal antibodies and allergen immunotherapies designed to counteract Th2-driven inflammation, as well as reflect on the need to investigate how these biologics impact Tfh cell activity, differentiation, and function, as these insights could pave the way for much-needed therapeutic innovation in the treatment of allergic diseases.

摘要

特应性被认为是21世纪的流行病,虽然数十年的研究已确立了驱动致病性IgE介导的过敏性疾病的Th2细胞之间的直接联系,但直到最近几年,滤泡辅助性T(Tfh)细胞才成为这些反应的关键驱动因素。在本综述中,我们将研究调控IgE反应的分子机制,特别强调关键细胞因子和信号通路。我们将讨论产生IgE的B细胞被排除在生发中心之外的情况,并探讨滤泡T细胞功能和异质性在驱动或抑制这些免疫反应方面最近确立的作用。此外,我们将评估旨在对抗Th2驱动的炎症的主要单克隆抗体和变应原免疫疗法的现状,并思考研究这些生物制剂如何影响Tfh细胞活性、分化和功能的必要性,因为这些见解可能为过敏性疾病治疗中急需的治疗创新铺平道路。

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