{"title":"治疗自身免疫性疾病的 CAR T 疗法的未来。","authors":"Ann-Christin Pecher, Luca Hensen, Claudia Lengerke, Jörg Henes","doi":"10.1007/s40291-024-00730-0","DOIUrl":null,"url":null,"abstract":"<p><p>The concept of chimeric antigen receptor (CAR) T cell therapy emerged from cancer immunotherapy and has been rapidly adapted and developed for the treatment of autoimmune, especially B-cell-driven, diseases since the first publication of an article featuring a patient with systemic lupus erythematosus in 2021. Phase II studies are about to start, but up to now, only case reports and small series have been published. In contrast to hemato-oncological diseases, where an aggressive response to malignant cells and long-lasting persistence of CAR T cells has been aimed at and observed in many patients, this is not the case with autoimmune diseases but might not be necessary to control disease. Future studies will focus on the optimal target but also on the optimal level of immunogenicity. The latter can be influenced by numerous modulations that affect not only cytokine release but also regulation. In addition, there are potential applications in regulatory cells such as CAR regulatory T cells (Treg). The question of toxicity reduction must also be addressed, as long-term complications such as the potential development of malignant diseases, infections, or cytopenia must be considered even more critically in the area of autoimmune diseases than is the case for patients with oncologic diseases. Alternative antibody-based therapies using the same target (e.g., CD3/CD19 bispecific targeting antibodies) have not been used in these patients and might also be considered in the future. In conclusion, CAR T cell therapy represents a promising therapeutic approach for autoimmune diseases, offering a targeted strategy to modulate immune responses and restore immune tolerance.</p>","PeriodicalId":49797,"journal":{"name":"Molecular Diagnosis & Therapy","volume":" ","pages":"593-600"},"PeriodicalIF":4.1000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11349844/pdf/","citationCount":"0","resultStr":"{\"title\":\"The Future of CAR T Therapeutics to Treat Autoimmune Disorders.\",\"authors\":\"Ann-Christin Pecher, Luca Hensen, Claudia Lengerke, Jörg Henes\",\"doi\":\"10.1007/s40291-024-00730-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The concept of chimeric antigen receptor (CAR) T cell therapy emerged from cancer immunotherapy and has been rapidly adapted and developed for the treatment of autoimmune, especially B-cell-driven, diseases since the first publication of an article featuring a patient with systemic lupus erythematosus in 2021. Phase II studies are about to start, but up to now, only case reports and small series have been published. In contrast to hemato-oncological diseases, where an aggressive response to malignant cells and long-lasting persistence of CAR T cells has been aimed at and observed in many patients, this is not the case with autoimmune diseases but might not be necessary to control disease. Future studies will focus on the optimal target but also on the optimal level of immunogenicity. The latter can be influenced by numerous modulations that affect not only cytokine release but also regulation. In addition, there are potential applications in regulatory cells such as CAR regulatory T cells (Treg). The question of toxicity reduction must also be addressed, as long-term complications such as the potential development of malignant diseases, infections, or cytopenia must be considered even more critically in the area of autoimmune diseases than is the case for patients with oncologic diseases. Alternative antibody-based therapies using the same target (e.g., CD3/CD19 bispecific targeting antibodies) have not been used in these patients and might also be considered in the future. 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引用次数: 0
摘要
嵌合抗原受体(CAR)T 细胞疗法的概念源于癌症免疫疗法,自 2021 年首次发表以一名系统性红斑狼疮患者为主角的文章以来,该疗法在治疗自身免疫性疾病(尤其是 B 细胞驱动的疾病)方面得到了迅速的调整和发展。二期研究即将开始,但到目前为止,只发表了病例报告和小型系列研究。与血液肿瘤疾病不同的是,CAR T 细胞的目标是对恶性细胞做出积极反应,并在许多患者身上观察到持久的持续性。未来的研究不仅要关注最佳靶点,还要关注免疫原性的最佳水平。后者会受到多种调节因素的影响,不仅会影响细胞因子的释放,还会影响调节。此外,CAR 调节性 T 细胞(Treg)等调节性细胞也有潜在的应用前景。减少毒性的问题也必须得到解决,因为在自身免疫性疾病领域,必须比肿瘤疾病患者更严格地考虑长期并发症,如潜在的恶性疾病、感染或细胞减少症。使用相同靶点的其他抗体疗法(如 CD3/CD19 双特异性靶向抗体)尚未在这些患者中使用过,将来可能也会考虑使用。总之,CAR T 细胞疗法是治疗自身免疫性疾病的一种很有前景的方法,它提供了一种调节免疫反应和恢复免疫耐受的靶向策略。
The Future of CAR T Therapeutics to Treat Autoimmune Disorders.
The concept of chimeric antigen receptor (CAR) T cell therapy emerged from cancer immunotherapy and has been rapidly adapted and developed for the treatment of autoimmune, especially B-cell-driven, diseases since the first publication of an article featuring a patient with systemic lupus erythematosus in 2021. Phase II studies are about to start, but up to now, only case reports and small series have been published. In contrast to hemato-oncological diseases, where an aggressive response to malignant cells and long-lasting persistence of CAR T cells has been aimed at and observed in many patients, this is not the case with autoimmune diseases but might not be necessary to control disease. Future studies will focus on the optimal target but also on the optimal level of immunogenicity. The latter can be influenced by numerous modulations that affect not only cytokine release but also regulation. In addition, there are potential applications in regulatory cells such as CAR regulatory T cells (Treg). The question of toxicity reduction must also be addressed, as long-term complications such as the potential development of malignant diseases, infections, or cytopenia must be considered even more critically in the area of autoimmune diseases than is the case for patients with oncologic diseases. Alternative antibody-based therapies using the same target (e.g., CD3/CD19 bispecific targeting antibodies) have not been used in these patients and might also be considered in the future. In conclusion, CAR T cell therapy represents a promising therapeutic approach for autoimmune diseases, offering a targeted strategy to modulate immune responses and restore immune tolerance.
期刊介绍:
Molecular Diagnosis & Therapy welcomes current opinion articles on emerging or contentious issues, comprehensive narrative reviews, systematic reviews (as outlined by the PRISMA statement), original research articles (including short communications) and letters to the editor. All manuscripts are subject to peer review by international experts.