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:Encephalopathy Post CAR-T Cell Therapy in Relapsed/Refractory Multiple Myeloma: Beyond ICANS.
Encephalopathy Post CAR-T Cell Therapy in Relapsed/Refractory Multiple Myeloma: Beyond ICANS.
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人类疱疹病毒6型(HHV-6)再激活是CAR-T 细胞治疗中罕见但严重的并发症,可与免疫效应细胞相关神经毒性综合征(ICANS)或细胞因子释放综合征(CRS)重叠,使诊断和管理具有挑战性。
我们描述了一名68岁复发/难治性IgA kappa多发性骨髓瘤男性患者,既往接受过多种治疗,包括CyBorD、mVRD-lite、Dara-CyBorD、VD-ACE和KPd,随后接受淋巴细胞清除性化疗和CAR-T 输注。输注后早期,他出现了2级CRS和ICANS,经托珠单抗和糖皮质激素治疗后改善,随后出现复发性脑病并伴有进行性神经功能下降。初始感染评估为阴性,但重复脑脊液(CSF)和血浆聚合酶链反应检测显示HHV-6再激活。开始使用膦甲酸抗病毒治疗,后改为更昔洛韦,并联合糖皮质激素和静脉注射免疫球蛋白。尽管重复CSF检测显示短暂的病毒清除,但神经功能持续下降,脑MRI显示与ICANS一致的发现,包括散在的白质信号异常和硬脑膜强化。尽管进行了积极管理,患者仍出现多器官衰竭并死亡。本病例说明了CAR-T 治疗期间HHV-6再激活的诊断复杂性,其与ICANS重叠的临床和影像学特征可能掩盖识别;既往治疗导致的深度免疫抑制和CAR-T 诱导的免疫失调可能易导致病毒再激活。HHV-6再激活是CAR-T 治疗后神经毒性的一个关键但未被充分认识的原因,临床医生对迟发性或非典型神经毒性患者应保持高度警惕,因为早期病毒学检测和及时抗病毒治疗可能改善这一脆弱人群的结局。
Human herpesvirus 6 (HHV-6) reactivation is a rare but serious complication of chimeric antigen receptor T-cell (CAR-T) therapy that can overlap with immune effector cell-associated neurotoxicity syndrome (ICANS) or cytokine release syndrome (CRS), making diagnosis and management challenging.
We describe a 68-year-old man with relapsed/refractory IgA kappa multiple myeloma who received multiple prior therapies, including CyBorD, mVRD-lite, Dara-CyBorD, VD-ACE, and KPd, before undergoing lymphodepleting chemotherapy and CAR-T infusion. Early after infusion he developed grade 2 CRS and ICANS that improved with tocilizumab and corticosteroids, followed by recurrent encephalopathy with progressive neurologic decline. Initial infectious evaluation was negative, but repeat cerebrospinal fluid (CSF) and plasma polymerase chain reaction testing revealed HHV-6 reactivation. Antiviral therapy with foscarnet, later switched to ganciclovir, was initiated with corticosteroids and intravenous immunoglobulin.
Although repeat CSF testing showed transient viral clearance, neurologic function continued to decline, and brain MRI demonstrated findings consistent with ICANS, including scattered white matter signal abnormalities and dural enhancement. Despite aggressive management, the patient developed multiorgan failure and died.
This case illustrates the diagnostic complexity of HHV-6 reactivation during CAR-T therapy, where overlapping clinical and radiologic features with ICANS can obscure recognition; profound immunosuppression from prior treatment and CAR-T-induced immune dysregulation likely predisposed to viral reactivation.
HHV-6 reactivation is a critical, underrecognized cause of neurotoxicity after CAR-T therapy, and clinicians should maintain a high index of suspicion in patients with delayed or atypical neurotoxicity, since early virologic testing and prompt antiviral therapy may improve outcomes in this vulnerable population.
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