决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:First third-generation CAR T cell application targeting CD19 for the treatment of systemic IgM AL amyloidosis with underlying marginal zone lymphoma.
我们报告一例新型病例:采用第三代 CD19 靶向 CAR-T 细胞输注治疗伴有分泌活性 B 细胞淋巴瘤的 AL 淀粉样变性,显示这是一种有效的治疗方式,可应用于继发 AL 淀粉样变性的患者。
轻链淀粉样变性(AL)是一种罕见疾病,由错误折叠的游离轻链在全身广泛沉积所致。伴免疫球蛋白M(IgM)单克隆丙种球蛋白病及边缘区淋巴瘤(MZL)等惰性B细胞淋巴瘤的患者有时可发生AL淀粉样变性。此前AL淀粉样变性CAR-T病例报告仅使用B细胞成熟抗原作为靶点,尚未采用CD19。本研究报告一名71岁男性病例,诊断为系统性AL κ型淀粉样变性及MZL,接受靶向CD19的第三代CAR-T治疗。既往治疗包括苯达莫司汀/利妥昔单抗、环磷酰胺/地塞米松,随后接受自体干细胞移植。尽管患者存在心脏和肾脏淀粉样变性表现,CAR-T治疗仍耐受良好,仅发生早期低级别治疗相关毒性。从第+30天起,患者IgM、κ轻链及κ/λ轻链差值持续下降,治疗6个月后达到深度血液学应答。总之,本病例首次展示了针对伴分泌活跃B细胞淋巴瘤的AL淀粉样变性患者实施第三代CD19 CAR-T治疗,提示该治疗方式有效且可用于继发AL淀粉样变性的患者。
Light chain amyloidosis (AL) is a rare disease caused by the generalized deposition of misfolded free light chains. Patients with immunoglobulin M gammopathy (IgM) and indolent B-cell lymphoma such as marginal zone lymphoma (MZL) may in some instances develop AL amyloidosis. So far, CAR T cells for AL amyloidosis have only been reported utilizing the B cell maturation antigen as target, while CD19 has so far not been used in AL amyloidosis.We report the case of a 71-year-old male, diagnosed with systemic AL kappa amyloidosis and MZL, receiving third-generation CAR T cell therapy targeting CD19. Prior treatment included bendamustine/rituximab and cyclophosphamide/ dexamethasone with subsequent autologous stem cell transplantation. CAR T application was well tolerated despite heart and kidney amyloid manifestations, and only early low-grade procedure-specific toxicities were observed. A continuous decrease in IgM, kappa light chains and kappa-to-lambda light chain difference was observed in the patient from day + 30 on, resulting in a deep hematological response six months after treatment.In summary, we present a novel case of CAR T cell treatment with third generation CD19 directed infusion for AL amyloidosis with an underlying secretory active B cell lymphoma, showing that this is an effective treatment modality and can be applied to patients with subsequent AL amyloidosis.
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