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评估生成白血病反应性细胞毒性T淋巴细胞系用于治疗异基因干细胞移植后复发白血病患者的I/II期可行性研究。

Phase I/II feasibility study evaluating the generation of leukemia-reactive cytotoxic T lymphocyte lines for treatment of patients with relapsed leukemia after allogeneic stem cell transplantation.

作者信息

Marijt Erik, Wafelman Amon, van der Hoorn Menno, van Bergen Cornelis, Bongaerts Rian, van Luxemburg-Heijs Simone, van den Muijsenberg Joost, Wolbers Judith Olde, van der Werff Nicole, Willemze Roel, Falkenburg Frederik

机构信息

Department of Hematology, Leiden University Medical Center, PO Box 9600, 2300 RC Leiden, The Netherlands.

出版信息

Haematologica. 2007 Jan;92(1):72-80. doi: 10.3324/haematol.10433.

Abstract

BACKGROUND AND OBJECTIVES

Graft-versus-host-disease may be avoided and the likelihood of a graft-versus-leukemia reaction increased by infusion of in vitro generated, leukemia-reactive, cytotoxic T lymphocyte (CTL) lines as treatment for patients with relapsed leukemia after allogeneic stem cell transplantation, instead of donor lymphocyte infusion. The aim of this study phase I/II study was to assess the feasibility of large-scale in vitro generation of leukemia-reactive CTL for clinical use.

DESIGN AND METHODS

Using a modified limiting dilution culture system donor T cells were stimulated with HLA-identical leukemic antigen presenting cells. Feasibility experiments demonstrated that in 16 of 27 donor-recipient pairs tested a CTL line could be generated. Twelve of these 16 patients developed a relapse and for 11 of these 12 patients a CTL line was generated under Good Manufacturing Practice conditions.

RESULTS

The CTL lines showed moderate to high cytotoxic activity against original recipient leukemic cells in vitro. Eight patients with a relapse received from one to seven CTL lines. One patient entered a complete remission after CTL infusion only, one entered a complete remission after combined CTL infusion and donor lymphocyte infusion, two patients had temporarily stable disease, and in four patients no response was observed.

INTERPRETATION AND CONCLUSIONS

Although the current procedure to generate these CTL lines is feasible, the strategy is logistically complex and time-consuming, and needs further improvement. Key words: cellular immunotherapy, CTL, leukemia, allogeneic stem cell transplantation.

摘要

背景与目的

通过输注体外产生的、白血病反应性细胞毒性T淋巴细胞(CTL)系,而非供体淋巴细胞输注,作为异基因干细胞移植后复发白血病患者的治疗手段,可避免移植物抗宿主病并提高移植物抗白血病反应的可能性。本I/II期研究的目的是评估大规模体外产生用于临床的白血病反应性CTL的可行性。

设计与方法

使用改良的有限稀释培养系统,用HLA相同的白血病抗原呈递细胞刺激供体T细胞。可行性实验表明,在测试的27对供体-受体对中,有16对能够产生CTL系。这16例患者中有12例复发,其中11例在药品生产质量管理规范条件下产生了CTL系。

结果

CTL系在体外对原受体白血病细胞表现出中度至高细胞毒性活性。8例复发患者接受了1至7个CTL系治疗。1例患者仅在输注CTL后进入完全缓解期,1例在联合输注CTL和供体淋巴细胞后进入完全缓解期,2例患者病情暂时稳定,4例患者无反应。

解读与结论

尽管目前产生这些CTL系的方法是可行的,但该策略在后勤方面复杂且耗时,需要进一步改进。关键词:细胞免疫疗法、CTL、白血病、异基因干细胞移植。

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