Protić-Rosić Isidora, Sehgal Al Nasar Ahmed, Wrighton Sebastian, Heller Birgit, Pickl Winfried F
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.
Cells. 2025 May 21;14(10):753. doi: 10.3390/cells14100753.
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.
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。