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:Torque Teno Virus plasma DNA load: a novel prognostic biomarker in CAR-T therapy.
Torque Teno Virus plasma DNA load: a novel prognostic biomarker in CAR-T therapy.
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Torque Teno病毒(TTV)是一种单链环状DNA病毒,已被确定为移植患者免疫能力的替代标志物。本研究调查了79例接受CAR-T 细胞治疗的复发/难治性大B细胞淋巴瘤成人患者血浆TTV DNA血症的动态变化,并评估TTV对免疫毒性、治疗应答及生存结局的影响。淋巴细胞清除治疗后,TTV DNA载量略有下降,约在第10天达到最低点,随后稳步升高,约在第90天达到峰值。免疫效应细胞相关神经毒性综合征(ICANS)发生时,TTV DNA载量低于4.05 log10拷贝/mL可识别有进展为重度ICANS风险的患者(OR=16.68,P=0.048)。
此外,从淋巴细胞清除至CAR-T 输注期间TTV DNA载量下降或保持稳定的患者,其无进展生存期优于载量上升的患者(HR=0.31,P=0.006)。这些发现提示,监测TTV可能作为免疫能力的替代指标,从而帮助预测CAR-T 疗效和毒性。此方法可能推动开发TTV指导的治疗策略,根据血浆TTV载量调整临床管理,类似于实体器官移植受者中提出的策略。
Torque Teno Virus (TTV) is a single-stranded circular DNA virus which has been identified as a surrogate marker of immune competence in transplantation. In this study we investigated the dynamics of plasma TTV DNAemia in 79 adult patients undergoing chimeric antigen receptor T-cell (CAR-T) therapy for relapsed or refractory large B-cell lymphoma, also evaluating the impact of TTV on immunotoxicities, response and survival outcomes.
After lymphodepleting therapy, TTV DNA load was found to decrease slightly until reaching nadir around day 10, after which it increased steadily until reaching maximum load around day 90. TTV DNA load < 4. 05 log10 copies/ml at immune effector cell-associated neurotoxicity syndrome (ICANS) onset identified patients at risk of progressing to severe forms of ICANS (OR 16. 68, P = 0. 048).
Finally, patients who experienced falling or stable TTV DNA load between lymphodepletion and CAR-T infusion had better progression-free survival than those with ascending TTV DNA load (HR 0. 31, P = 0. 006).
These findings suggest that TTV monitoring could serve as a surrogate marker of immune competence, enabling predictions of CAR-T efficacy and toxicity. This could pave the way for the development of TTV-guided therapeutic strategies that modulate clinical patient management based on plasma TTV load, similar to suggested strategies in solid organ transplant recipients.
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