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肽段选择的 T 细胞移植后对 EBV-PTLD 的有效和长期控制。

Effective and long-term control of EBV PTLD after transfer of peptide-selected T cells.

机构信息

Clinical Cooperation Group Molecular Oncology, Helmholtz Zentrum München and Ludwig-Maximilians-Universität, Munich, Germany.

出版信息

Blood. 2010 Apr 8;115(14):2960-70. doi: 10.1182/blood-2009-08-236356. Epub 2010 Jan 26.

Abstract

Posttransplantation lymphoproliferative disease (PTLD) associated with Epstein-Barr virus (EBV) is a life-threatening complication after allogeneic hematopoietic stem cell transplantation. PTLD is efficiently prevented by adoptive transfer of EBV-specific T cells from the donor. To make EBV-specific T cells available in urgent clinical situations, we developed a rapid protocol for their isolation by overnight stimulation of donor blood cells with peptides derived from 11 EBV antigens, interferon-gamma surface capture, and immunomagnetic separation. Six patients with PTLD received 1 transfusion of EBV-specific T cells. No response was seen in 3 patients who had late-stage disease with multiorgan dysfunction at the time of T-cell transfer. In 3 patients who received T cells at an earlier stage of disease, we observed complete and stable remission of PTLD. Two patients have remained free from EBV-associated disease for more than 2 years. CD8(+) T cells specific for EBV early antigens rapidly expanded after T-cell transfer, temporarily constituted greater than 20% of all peripheral blood lymphocytes, and were maintained throughout the observation period. Thus, a rapid and sustained reconstitution of a protective EBV-specific T-cell memory occurred after the infusion of small numbers of directly isolated EBV-specific T cells.

摘要

移植后淋巴组织增生性疾病(PTLD)与 EBV 相关,是异基因造血干细胞移植后的一种危及生命的并发症。通过从供体中过继转移 EBV 特异性 T 细胞,可以有效地预防 PTLD。为了在紧急临床情况下获得 EBV 特异性 T 细胞,我们开发了一种快速方案,通过 overnight 刺激供体血细胞与来自 11 种 EBV 抗原的肽、干扰素-γ表面捕获和免疫磁分离来分离 EBV 特异性 T 细胞。6 名患有 PTLD 的患者接受了 1 次 EBV 特异性 T 细胞输注。在 T 细胞转移时患有多器官功能障碍的晚期疾病的 3 名患者中未观察到反应。在 3 名在疾病早期接受 T 细胞的患者中,我们观察到 PTLD 完全和稳定缓解。2 名患者已超过 2 年没有 EBV 相关疾病。T 细胞转移后,针对 EBV 早期抗原的 CD8(+) T 细胞迅速扩增,暂时构成外周血淋巴细胞的 20%以上,并在整个观察期间维持。因此,输注少量直接分离的 EBV 特异性 T 细胞后,会迅速而持续地重建保护性 EBV 特异性 T 细胞记忆。

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