CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Advancing CAR T cell therapy through the use of multidimensional omics data.
Advancing CAR T cell therapy through the use of multidimensional omics data.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
尽管嵌合抗原受体(CAR)T细胞疗法治疗某些血液系统恶性肿瘤取得显著成功,但仍面临诸多挑战,包括优化CAR设计和细胞产品、提高缓解率、延长缓解持久性、降低毒性,以及拓展这种治疗方式在其他癌症类型中的应用。基因组学、表观基因组学、转录组学、T细胞受体库分析、蛋白质组学、代谢组学和/或微生物组学等多维组学数据,为解析CAR-T 细胞复杂且动态的多因素表型、过程和反应提供了独特机会,也有助于发现新的肿瘤靶点和耐药通路。本综述总结用于推动CAR-T 细胞疗法机制理解的多维细胞和分子分析技术,并讨论多组学数据的当前应用及潜在策略,以鉴定最佳靶抗原和其他可利用的分子特征,从而增强CAR-T 细胞疗法抗肿瘤活性并降低毒性。充分利用多组学数据将为CAR-T 细胞疗法生物学带来新认识,进一步加速开发疗效和安全性更佳的产品,并帮助临床医生更好地预测和监测患者反应。
Despite the notable success of chimeric antigen receptor (CAR) T cell therapies in the treatment of certain haematological malignancies, challenges remain in optimizing CAR designs and cell products, improving response rates, extending the durability of remissions, reducing toxicity and broadening the utility of this therapeutic modality to other cancer types.
Data from multidimensional omics analyses, including genomics, epigenomics, transcriptomics, T cell receptor-repertoire profiling, proteomics, metabolomics and/or microbiomics, provide unique opportunities to dissect the complex and dynamic multifactorial phenotypes, processes and responses of CAR T cells as well as to discover novel tumour targets and pathways of resistance.
In this Review, we summarize the multidimensional cellular and molecular profiling technologies that have been used to advance our mechanistic understanding of CAR T cell therapies.
In addition, we discuss current applications and potential strategies leveraging multi-omics data to identify optimal target antigens and other molecular features that could be exploited to enhance the antitumour activity and minimize the toxicity of CAR T cell therapy. Indeed, fully utilizing multi-omics data will provide new insights into the biology of CAR T cell therapy, further accelerate the development of products with improved efficacy and safety profiles, and enable clinicians to better predict and monitor patient responses.
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