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异基因细胞毒性T细胞疗法治疗EBV阳性移植后淋巴细胞增殖性疾病:一项2期多中心临床试验的结果

Allogeneic cytotoxic T-cell therapy for EBV-positive posttransplantation lymphoproliferative disease: results of a phase 2 multicenter clinical trial.

作者信息

Haque Tanzina, Wilkie Gwen M, Jones Marie M, Higgins Craig D, Urquhart Gillian, Wingate Phoebe, Burns David, McAulay Karen, Turner Marc, Bellamy Christopher, Amlot Peter L, Kelly Deirdre, MacGilchrist Alastair, Gandhi Maher K, Swerdlow Anthony J, Crawford Dorothy H

机构信息

Clinical and Molecular Virology Laboratory, University of Edinburgh, Edinburgh, United Kingdom.

出版信息

Blood. 2007 Aug 15;110(4):1123-31. doi: 10.1182/blood-2006-12-063008. Epub 2007 Apr 27.

DOI:10.1182/blood-2006-12-063008
PMID:17468341
Abstract

We present the results of a multicenter clinical trial using Epstein-Barr virus (EBV)-specific cytotoxic T lymphocytes (CTLs) generated from EBV-seropositive blood donors to treat patients with EBV-positive posttransplantation lymphoproliferative disease (PTLD) on the basis of the best HLA match and specific in vitro cytotoxicity. Thirty-three PTLD patients who had failed on conventional therapy were enrolled. No adverse effects of CTL infusions were observed and the response rate (complete or partial) in 33 patients was 64% at 5 weeks and 52% at 6 months. Fourteen patients achieved a complete remission, 3 showed a partial response, and 16 had no response at 6 months (5 died before completing treatment). At 5 weeks, there was a significant trend toward better responses with higher numbers of CD4(+) cells in infused CTL lines (P = .001) that were maintained at 6 months (P = .001). Patients receiving CTLs with closer HLA matching responded better at 6 months (P = .048). Female patients responded better than male patients, but the differences were not statistically significant. Our results show that allogeneic CTLs are a safe and rapid therapy for PTLD, bypassing the need to grow CTLs for individual patients. The response rate in this poor prognosis patient group is encouraging.

摘要

我们展示了一项多中心临床试验的结果,该试验使用从EB病毒(EBV)血清反应阳性献血者中产生的EBV特异性细胞毒性T淋巴细胞(CTL),基于最佳的HLA匹配和特定的体外细胞毒性来治疗EBV阳性移植后淋巴细胞增生性疾病(PTLD)患者。33例传统治疗失败的PTLD患者入组。未观察到CTL输注的不良反应,33例患者在5周时的缓解率(完全或部分缓解)为64%,6个月时为52%。14例患者达到完全缓解,3例显示部分缓解,16例在6个月时无反应(5例在完成治疗前死亡)。在5周时,输注的CTL系中CD4(+)细胞数量越多,缓解趋势越明显(P = .001),这种趋势在6个月时仍持续(P = .001)。HLA匹配更接近的患者接受CTL治疗在6个月时反应更好(P = .048)。女性患者的反应优于男性患者,但差异无统计学意义。我们的结果表明,同种异体CTL是一种安全、快速的PTLD治疗方法,无需为个体患者培养CTL。该预后不良患者组的缓解率令人鼓舞。

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