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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Neurological Adverse Effects of Immune Checkpoint Inhibitors and Chimeric Antigen Receptor T-Cell Therapy.
Neurological Adverse Effects of Immune Checkpoint Inhibitors and Chimeric Antigen Receptor T-Cell Therapy.
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免疫检查点抑制剂(ICPIs)和嵌合抗原受体(CAR)T细胞是近期获批的新型疗法,靶向治疗多种恶性肿瘤。这两种治疗均调节免疫系统,并可导致多种免疫相关不良事件(irAEs),包括多内分泌腺病、胃肠道及神经系统并发症。本文献综述聚焦于这些疗法的神经系统副作用,因其较为罕见且会改变治疗进程。神经系统并发症涉及周围和中枢神经系统,包括多发性神经病、肌炎、重症肌无力、脱髓鞘性多神经根病、脊髓炎和脑炎。若早期识别,神经系统并发症可通过类固醇有效治疗,以降低短期和长期并发症的潜在风险。因此,需要早期识别和治疗irAEs,以优化与ICPI和CAR-T 细胞疗法相关的结局。
Immune checkpoint inhibitors (ICPIs) and chimeric antigen receptor (CAR) T-cell constitute recently approved novel therapies targeted to treat a wide number of malignancies. Both the treatments modulate the immune system and can cause a number of immune-related adverse events (irAEs), including polyendocrinopathies, gastrointestinal and neurological complications.
This literature review focuses on the neurological side effects of these therapies as these are uncommon and alter the course of the treatment. Neurological complications involve the peripheral and central nervous system, including polyneuropathy, myositis, myasthenia gravis, demyelinating polyradiculopathy, myelitis, and encephalitis. If early recognized, the neurological complications can be treated effectively with steroids to reduce the potential of short-term and long-term complications.
Therefore, early identification and treatment of irAEs are needed to optimize the outcomes associated with ICPI and CAR T-cell therapies.
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