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首页> 外文期刊>Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation >Cytomegalovirus-specific cytotoxic t lymphocytes can be efficiently expanded from granulocyte colony-stimulating factor-mobilized hemopoietic progenitor cell products ex vivo and safely transferred to stem cell transplantation recipients to facilitate immune reconstitution
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Cytomegalovirus-specific cytotoxic t lymphocytes can be efficiently expanded from granulocyte colony-stimulating factor-mobilized hemopoietic progenitor cell products ex vivo and safely transferred to stem cell transplantation recipients to facilitate immune reconstitution

机译:巨细胞病毒特异的细胞毒性t淋巴细胞可以从粒细胞集落刺激因子动员的造血祖细胞产物中有效地离体扩增,并安全地转移到干细胞移植受者中,以促进免疫重建

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摘要

Uncontrolled cytomegalovirus (CMV) reactivation after allogeneic hematopoietic stem cell transplantation causes significant morbidity and mortality. Adoptive transfer of CMV-specific cytotoxic T lymphocytes (CTLs) is a promising therapy to treat reactivation and prevent viral disease. In this article, we describe the generation of clinical-grade CMV-specific CTLs directly from granulocyte colony-stimulating factor-mobilized hemopoietic progenitor cell (G-HPC) products collected for transplantation. This method requires less than 2.5% of a typical G-HPC product to reproducibly expand CMV-specific CTLs ex vivo. Comparison of 11 CMV CTL lines generated from G-HPC products with 52 CMV CTL lines generated from nonmobilized peripheral blood revealed similar expansion kinetics and phenotype. G-HPC-derived CTLs produced IFN-γ after reexposure to CMVpp65 antigen and exhibited CMV-directed cytotoxicity but no alloreactivity against transplantation recipient-derived cells. Seven patients received CMV-specific CTL lines expanded from G-HPC products in a prophylactic adoptive immunotherapy phase I/II clinical trial. Use of G-HPC products will facilitate integration of CTL generation into established quality systems of transplantation centers and more rapid inclusion of T cell therapies into routine clinical care.
机译:异基因造血干细胞移植后不受控制的巨细胞病毒(CMV)的重新激活会导致明显的发病率和死亡率。 CMV特异性细胞毒性T淋巴细胞(CTL)的过继转移是治疗再激活和预防病毒性疾病的有前途的疗法。在本文中,我们描述了直接从收集用于移植的粒细胞集落刺激因子动员的造血祖细胞(G-HPC)产品中直接生成临床级CMV特异性CTL的过程。此方法需要不到典型G-HPC产品的2.5%才能可复制地扩增离体的CMV特异性CTL。从G-HPC产品生成的11个CMV CTL谱系与从未动员的外周血生成的52个CMV CTL谱系进行比较,发现相似的扩增动力学和表型。 G-HPC衍生的CTL在再暴露于CMVpp65抗原后产生IFN-γ,并表现出CMV定向的细胞毒性,但对移植受体衍生的细胞没有同种反应性。在预防性过继免疫疗法I / II期临床试验中,有7名患者接受了从G-HPC产品扩展而来的CMV特异性CTL品系。使用G-HPC产品将有助于将CTL生成整合到已建立的移植中心质量体系中,并将T细胞疗法更快地纳入常规临床护理中。

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