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Chimeric antigen receptors: unleashing a new age of anti-cancer therapy

机译:嵌合抗原受体:释放抗癌治疗的新时代

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Chimeric antigen receptors (CARs) represent a novel facet of modern day synthetic biology that exemplifies personalized medicine at work through their ability to harness and redirect a patient’s immune system to fight cancer. By combining the target-specificity of antibodies to the effector capabilities of T cells, CARs have yielded high remission rates for many late staged and relapsed/refractory (r/r) hematological malignancies, including acute lymphoblastic leukemias (ALL) and Non-Hodgkin’s lymphomas. Despite toxicities of cytokine release syndrome and neurotoxicity, recent studies have uncovered their underlying mechanisms and devised effective therapies to manage and possibly prevent them. In 2017, CAR T cell therapy became a reality for the general public despite the high costs, when Novartis’s Kymriah, became the first product to receive FDA approval for pediatric r/r B cell ALL with Gilead’s Yescarta following several months later. Although effective in hematological malignancies, CAR response has been limited in solid tumors largely attributed to the heterogeneous and immunosuppressive tumor microenvironment along tumor defense mechanisms, such as antigenic escape. Despite the current challenges of CAR T therapy, this technology is still in its infancy and its promise will continue to grow as scientists continue to develop novel approaches to enhance its efficacy. As its prevalence continues to increase, institutions and pharmaceuticals worldwide are investing in this technology in hopes of driving therapeutic innovation, while providing greater access to their respective populations through clinical trials.
机译:嵌合抗原受体(CARs)代表了现代合成生物学的一个新方面,通过其利用和调节患者免疫系统抵抗癌症的能力,可以例证个性化药物在工作中。通过结合抗体对T细胞效应子功能的靶标特异性,CARs对许多晚期和复发/难治性(r / r)血液恶性肿瘤(包括急性淋巴细胞白血病(ALL)和非霍奇金淋巴瘤)产生了高缓解率。尽管细胞因子释放综合征和神经毒性具有毒性,但最近的研究发现了其潜在机制,并设计了有效的疗法来管理和预防它们。 2017年,尽管成本高昂,但CAR T细胞疗法仍然成为普通大众的选择,几个月后,诺华的Kymriah成为第一个通过Gilead的Yescarta获得FDA批准的小儿R / r B细胞ALL的产品。尽管在血液系统恶性肿瘤中有效,但CAR反应在实体瘤中受到限制,这在很大程度上归因于沿肿瘤防御机制(如抗原逃逸)的异质性和免疫抑制性肿瘤微环境。尽管目前CAR T疗法面临挑战,但这项技术仍处于起步阶段,随着科学家继续开发提高其功效的新方法,其前景将继续增长。随着其普及率的不断提高,全世界的机构和制药公司都在对该技术进行投资,以期推动治疗创新,同时通过临床试验为他们各自的人群提供更多的机会。

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