Suppr超能文献

基于嵌合自身抗体受体和/或肽-主要组织相容性复合体的嵌合抗原受体疗法,用于在过敏和自身免疫性疾病等超敏反应性疾病中靶向清除抗原特异性B细胞或T细胞。

Chimeric Autoantibody Receptor- and/or Peptide-MHC-Based CAR Therapies for Targeted Elimination of Antigen-Specific B or T Cells in Hypersensitivity Disorders Such as Allergies and Autoimmune Diseases.

作者信息

Protić-Rosić Isidora, Sehgal Al Nasar Ahmed, Wrighton Sebastian, Heller Birgit, Pickl Winfried F

机构信息

Center for Pathophysiology, Infectiology and Immunology, Institute of Immunology, Medical University of Vienna, 1090 Vienna, Austria.

Faculty of Chemistry, University of Belgrade, 11000 Belgrade, Serbia.

出版信息

Cells. 2025 May 21;14(10):753. doi: 10.3390/cells14100753.

Abstract

Hypersensitivity reactions are dysregulated and potentially devastating immune responses, characterized by a tendency to become chronic. They target either self-proteins or harmless foreign proteins and are driven by both T and B cells. Although numerous symptomatic treatment options for hypersensitivity reactions have been established over recent decades, only a few antigen-specific, causal approaches capable of specifically targeting the pathogenic autoreactive T and/or B cells have been developed. Among these are cell-based treatment modalities involving chimeric antigen receptor (CAR)- or chimeric autoantibody-receptor (CAAR)-expressing cells. These therapies utilize B- or T-cell antigens, presented as B-cell epitopes or peptide-major histocompatibility complexes (pMHCs) to serve as bait. The latter are coupled to potent activation domains derived from the TCR/CD3 complex itself, such as the zeta or CD3 chains, as well as domains from bona fide co-stimulatory molecules (e.g., CD28, 4-1BB). Recent in vitro and in vivo studies have demonstrated the therapeutic potential of these ATMP-based strategies in eliminating autoreactive lymphocytes and alleviating hypersensitivity reactions. This systematic review provides a comprehensive overview of the current status of antigen-specific CAR and CAAR T-cell therapies, highlighting novel directions as well as the ongoing challenges within this promising research field.

摘要

超敏反应是失调且可能具有破坏性的免疫反应,其特点是易于发展为慢性反应。它们针对自身蛋白或无害的外来蛋白,由T细胞和B细胞共同驱动。尽管近几十年来已经确立了许多针对超敏反应的对症治疗方案,但仅开发出了少数几种能够特异性靶向致病性自身反应性T细胞和/或B细胞的抗原特异性、病因性治疗方法。其中包括基于细胞的治疗方式,涉及表达嵌合抗原受体(CAR)或嵌合自身抗体受体(CAAR)的细胞。这些疗法利用作为B细胞表位或肽-主要组织相容性复合体(pMHC)呈现的B细胞或T细胞抗原作为诱饵。后者与源自TCR/CD3复合体本身的强效激活结构域(如ζ链或CD3链)以及来自真正共刺激分子(如CD28、4-1BB)的结构域偶联。最近的体外和体内研究已经证明了这些基于先进治疗用药品(ATMP)的策略在消除自身反应性淋巴细胞和减轻超敏反应方面的治疗潜力。本系统综述全面概述了抗原特异性CAR和CAAR T细胞疗法的现状,突出了这一有前景的研究领域内的新方向以及持续存在的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d424/12110022/a21d45ec7ff9/cells-14-00753-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验