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:Treatment of Progressive Multifocal Leukoencephalopathy with Third-Party Allogeneic BK Virus T Cells.
Treatment of Progressive Multifocal Leukoencephalopathy with Third-Party Allogeneic BK Virus T Cells.
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这些数据表明,第三方 BK-VST 输注是安全的且可能有效,为这种原本致命的疾病提供了一种可扩展的免疫治疗方法支持。(ClinicalTrials.gov NCT02479698)。
进行性多灶性白质脑病(PML)是由JC多瘤病毒(JCV)引起的一种致死性脱髓鞘疾病,影响免疫抑制个体,目前尚无获批疗法。在此,我们评估第三方、即用型、部分HLA匹配的BK病毒特异性T细胞(BK-VST)在PML患者中的安全性和疗效。
我们开展了一项单中心2期研究,37例患者接受了HLA最匹配的BK-VST,剂量为2.0 x 105 T细胞/kg,未达到完全缓解的受试者允许额外输注。23例患者的基础诊断为血液系统恶性肿瘤。每例患者接受中位2剂(范围,1-12;IQR 2)。总体缓解(OR)定义为病毒学清除且神经系统稳定或改善。
在12个月的随访期间,21例患者(56.8%)达到OR,其中16例(43.2%)达到完全缓解。缓解迅速(中位23天)且持久,尽管HLA匹配有限,但未观察到缓解丧失。1年总生存率为61.1%(95% CI,41.9-77.4)。首次输注后达到OR的患者1年生存率较未缓解者显著改善(93.3% vs 0%;p<0.001)。较高的供者IL-2和IFN-γ产生T细胞频率以及更好的HLA匹配与临床获益相关。
Progressive multifocal leukoencephalopathy (PML) is a fatal demyelinating disease caused by JC polyomavirus (JCV) that affects immunosuppressed individuals and has no approved therapy. Here we evaluate the safety and efficacy of third-party, off-the-shelf, partially HLA-matched BK virus-specific T cells (BK-VST) in patients with PML.
We conducted a single-center phase 2 study where 37 patients received most closely HLA-matched BK-VST at 2.0 x 105 T cells/kg, with additional infusions permitted for subjects who did not achieve a complete response. Twenty-three patients had an underlying diagnosis of hematologic malignancy. Each patient received a median of 2 doses (range, 1-12; IQR 2). Overall response (OR) was defined as virologic clearance with neurologic stabilization or improvement.
During 12 months of follow-up, 21 patients (56.8%) achieved an OR, including 16 (43.2%) with a complete response. Responses were rapid (median 23 days) and durable, with no loss of response observed despite limited HLA matching. The 1-year overall survival was 61.1% (95% CI, 41.9-77.4). Patients achieving an OR after the first infusion had markedly improved 1-year survival compared with non-responders (93.3% vs 0%; p<0.001). Higher donor IL-2 and IFN-γ-producing T-cell frequencies and greater HLA matching correlated with clinical benefit.
These data demonstrate that third-party BK-VST infusions are safe and potentially effective, supporting a scalable immunotherapeutic approach for this otherwise fatal disease. (ClinicalTrials.gov NCT02479698).
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