儿童难治性重症肌无力的治疗进展
Progress in the Treatment of Refractory Myasthenia Gravis in Children
DOI: 10.12677/acm.2026.1631086, PDF,   
作者: 甘校铭, 曹 洁*:重庆医科大学附属儿童医院全科医学科,儿童少年健康与疾病国家临床医学研究中心,儿童发育疾病研究教育部重点实验室,儿童神经发育与认知障碍重庆市重点实验室,重庆
关键词: 儿童重症肌无力难治性生物制剂CAR-T细胞疗法胸腺切除术Myasthenia Gravis in Children Refractory Biological Agents CAR-T Cell Therapy Thymectomy
摘要: 重症肌无力(MG)是一种由多种抗体介导、细胞和体液免疫依赖、补体和细胞因子参与的神经–肌肉接头传递障碍的自身免疫性疾病。儿童MG在治疗上与成人有较大区别,而且目前临床仍缺乏针对儿童难治性MG统一的治疗方案。近年来,随着对MG发病机制进一步了解、新药物的研发应用、新理念的形成,给儿童难治性MG的诊疗带来了革命性的变化。本文阐述了儿童难治性MG在治疗方面的最新进展,包括新的生物制剂,如补体抑制剂、FcRn抑制剂、靶向B细胞药物等。
Abstract: Myasthenia gravis (MG) is an autoimmune disease mediated by cellular immunity, humoral immunity, complement and cytokines, which causes neuromuscular junction transmission disorders. Pediatric MG is different from adult MG in treatment. However, there is still a lack of a unified treatment plan for refractory MG in children. In recent years, the diagnosis and treatment of pediatric refractory MG have brought revolutionary changes, with the further understanding of the pathogenesis of MG, the development and application of new drugs, and the formation of new concepts. This article reviews recent advances in the treatment of pediatric refractory MG, including new biologics such as complement inhibitors, FcRn inhibitors, and B-cell targeting drugs.
文章引用:甘校铭, 曹洁. 儿童难治性重症肌无力的治疗进展[J]. 临床医学进展, 2026, 16(3): 2836-2845. https://doi.org/10.12677/acm.2026.1631086

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