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:The role of neurologists in the era of cancer immunotherapy: Focus on CAR T-cell therapy and immune checkpoint inhibitors.
The role of neurologists in the era of cancer immunotherapy: Focus on CAR T-cell therapy and immune checkpoint inhibitors.
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癌症免疫治疗代表了一种新型抗癌策略,直接作用于免疫系统,促进其向癌细胞活化,从而增强其天然抗癌能力。在当前使用或正在研究的各种治疗中,嵌合抗原受体(CAR)T细胞疗法和免疫检查点抑制剂(ICIs)始终证明其疗效。这些创新正在逐步改善癌症治疗的标准,然而它们受到新型神经系统不良事件的阻碍,使神经科医生在多学科肿瘤团队中发挥关键作用。事实上,高达77%接受CAR-T 细胞治疗的患者可能出现神经毒性,通常表现为以额叶功能障碍为主的大脑病。这种神经毒性与细胞因子释放综合征相关,后者是由CAR-T 细胞触发的全身性高炎症状态。另一方面,在接受ICIs治疗后,不受约束的T细胞可能通过抗原导向的自身免疫导致中枢和周围神经系统疾病。
值得注意的是,CAR-T 细胞治疗相关神经毒性与细胞因子风暴的神经系统表现(例如COVID-19相关大脑病)之间,以及ICIs相关神经系统不良事件的一个亚组与副肿瘤性神经系统综合征之间,已被强调存在生物学和临床相似性。
因此,这些癌症免疫治疗相关的神经系统综合征可能提供一个前所未有的、或许是暂时的机会,以阐明广泛神经系统综合征的潜在致病机制,并推动我们在神经免疫学方面的知识。
Cancer immunotherapy represents a novel anticancer strategy that acts directly on the immune system, promoting its activation toward cancer cells to enhance its natural ability to fight cancer. Among various treatments currently used or investigated, chimeric antigen receptors (CAR) T-cell therapy and immune checkpoint inhibitors (ICIs) have consistently proven their efficacy. These innovations are progressively improving the standard of care in cancer treatment, yet they are hampered by novel neurological adverse events, attributing to neurologists a key role in the multidisciplinary oncological team.
Indeed, neurotoxicity may develop in up to 77% of patients who received CAR T-cell therapy and usually presents with encephalopathy characterized by a predominant frontal lobe dysfunction. This neurotoxicity is related to cytokine release syndrome, a systemic hyperinflammatory condition triggered by CAR T-cells. On the other hand, following treatment with ICIs, unrestrained T-cells may lead to central and peripheral neurological disorders by antigen-directed autoimmunity.
Notably, biological and clinical similarities have been underlined between neurotoxicity related to CAR T-cell therapy and neurological manifestations of cytokine storms (e. g. COVID-19-related encephalopathy), as well as between a subgroup of ICI-related neurological adverse events and paraneoplastic neurological syndromes.
Therefore, these cancer immunotherapy-related neurological syndromes may provide an unprecedented, perhaps transitory, opportunity to shed light on the underlying pathogenic mechanisms of a wide spectrum of neurological syndromes and to push forward our knowledge in neuroimmunology.
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