Department I for Internal Medicine, Center of Molecular Medicine Cologne (CMMC), University Hospital of Colgne, Cologne, Germany.
Front Immunol. 2022 Aug 10;13:934343. doi: 10.3389/fimmu.2022.934343. eCollection 2022.
CAR (Chimeric Antigen Receptor) T-cell therapy has revolutionized the field of oncology in recent years. This innovative shift in cancer treatment also provides the opportunity to improve therapies for many patients suffering from various autoimmune diseases. Recent studies have confirmed the therapeutic suppressive potential of regulatory T cells (Tregs) to modulate immune response in autoimmune diseases. However, the polyclonal character of regulatory T cells and their unknown TCR specificity impaired their therapeutic potency in clinical implementation. Genetical engineering of these immune modulating cells to express antigen-specific receptors and using them therapeutically is a logical step on the way to overcome present limitations of the Treg strategy for the treatment of autoimmune diseases. Encouraging preclinical studies successfully demonstrated immune modulating properties of CAR Tregs in various mouse models. Still, there are many concerns about targeted Treg therapies relating to CAR target selectivity, suppressive functions, phenotype stability and safety aspects. Here, we summarize recent developments in CAR design, Treg biology and future strategies and perspectives in CAR Treg immunotherapy aiming at clinical translation.
嵌合抗原受体(CAR)T 细胞疗法近年来彻底改变了肿瘤学领域。这种癌症治疗的创新转变也为许多患有各种自身免疫性疾病的患者提供了改善治疗的机会。最近的研究证实了调节性 T 细胞(Tregs)在调节自身免疫性疾病中的免疫抑制潜力。然而,调节性 T 细胞的多克隆特性及其未知的 TCR 特异性限制了它们在临床实施中的治疗效果。对这些免疫调节细胞进行基因工程改造,使其表达抗原特异性受体,并将其用于治疗,是克服目前治疗自身免疫性疾病的 Treg 策略局限性的一种合理步骤。令人鼓舞的临床前研究成功地证明了 CAR Tregs 在各种小鼠模型中的免疫调节特性。然而,针对靶向 Treg 治疗的许多关注点与 CAR 靶向选择性、抑制功能、表型稳定性和安全性方面有关。在这里,我们总结了 CAR 设计、Treg 生物学以及 CAR Treg 免疫治疗的未来策略和观点的最新进展,旨在实现临床转化。