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Generation and administration of HA-1-specific T-cell lines for the treatment of patients with relapsed leukemia after allogeneic stem cell transplantation: a pilot study

机译:异基因干细胞移植后治疗复发性白血病患者HA-1特异性T细胞系的产生和给药:一项初步研究

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摘要

Since HA-1-specific T cells have been shown to make a significant contribution to the clinical responses in patients with relapsed leukemia, we investigated the feasibility of adoptive transfer of in vitro induced HA-1-specific CD8 positive T cells to patients with relapsed leukemia after allogeneic stem cell transplantation. The in vitro generation of clinical grade HA-1-specific T-cell lines from HA-1 negative donors was seen to be feasible and 3 patients were treated with HA-1-specific T-cell lines. No toxicity after infusion was observed. Although in one patient, during a period of stable disease, HA-1-specific T cells could be detected in the peripheral blood and bone marrow, these patients had no clear clinical response.
机译:由于已证明HA-1特异性T细胞对复发性白血病患者的临床反应具有重要作用,因此我们研究了将体外诱导的HA-1特异性CD8阳性T细胞过继转移到复发性白血病患者中的可行性。同种异体干细胞移植后发生白血病。从HA-1阴性供体体外产生临床等级的HA-1特异性T细胞系被认为是可行的,并用HA-1特异性T细胞系治疗了3例患者。输注后未观察到毒性。尽管在一名患者中,在疾病稳定期间,可以在外周血和骨髓中检测到HA-1特异性T细胞,但这些患者并没有明确的临床反应。

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