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:Human herpesvirus 6 (HHV-6) encephalitis secondary to chimeric antigen receptor (CAR)-T cell therapy.
Human herpesvirus 6 (HHV-6) encephalitis secondary to chimeric antigen receptor (CAR)-T cell therapy.
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继发于 CAR-T 细胞治疗的 HHV-6 脑炎可能容易与 ICANS 混淆。
嵌合抗原受体(CAR)T细胞治疗继发的人疱疹病毒(HHV)-6脑炎在临床实践中相对少见,需要与免疫效应细胞相关神经毒性综合征(ICANS)鉴别。
我们回顾性报告一例CAR-T 治疗继发HHV-6脑炎病例。
一名来自中国的弥漫大B细胞淋巴瘤男性患者接受CAR-T 治疗后,第8天出现全身性皮疹;治疗后第14天出现认知改变、记忆丧失和定向障碍。起初怀疑为ICANS。第18天进行腰椎穿刺。脑脊液(CSF)分析显示蛋白水平轻度升高,宏基因组二代测序(mNGS)检出大量HHV-6B序列。脑部MRI显示双侧海马异常。最终患者确诊HHV-6脑炎,并接受更昔洛韦和地塞米松治疗。治疗一周后,复查CSF显示HHV-6B序列减少。患者出院时记忆和定向力均有改善。
CAR-T 治疗继发HHV-6脑炎易与ICANS混淆。及时积极开展诊断检查(如CSF mNGS和颅脑影像学检查),并迅速启动抗病毒治疗,对于改善患者结局至关重要。
Human herpesvirus (HHV)-6 encephalitis secondary to chimeric antigen receptor (CAR)-T cell therapyis relatively rare in clinical practice and needs to be differentiated from immune effector cell-associatedneurotoxicity syndrome (ICANS).
We retrospectively reported a case of HHV-6 encephalitis secondary to CAR-T cell therapy.
A male patient from China with diffuse large B-cell lymphoma underwent chimeric CAR-T cell therapy anddeveloped a generalized rash on the 8 th day, followed by cognitive changes, memory loss, and disorientation onthe 14 th day after CAR-T cell therapy. Initially, ICANS was suspected. A lumbar puncture was performed on the 18 th day. The cerebrospinal fluid (CSF) analysis revealed slightly elevated protein levels and a high presence of HHV-6B sequences by mNGS. Brain MRI showed bilateral hippocampal abnormalities. The patient was ultimatelydiagnosed with HHV-6 encephalitis and treated with ganciclovir and dexamethasone. After one week of treatment,follow-up CSF analysis showed a reduction in HHV-6B sequences. The patient was discharged with improvedmemory and orientation.
HHV-6 encephalitis secondary to CAR-T cell therapy may be easily confused with ICANS. Timely andaggressive diagnostic procedures, such as mNGS of CSF and cranial imaging, along with prompt antiviral therapy,are crucial for improving patient outcomes.
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