首页> 外文期刊>Transplantation Proceedings >Antileukemic Effect of Interleukin-7-Transduced Bone Marrow Stromal Cells in Mice Following Allogeneic T-Cell-Depleted Bone Marrow Transplantation.
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Antileukemic Effect of Interleukin-7-Transduced Bone Marrow Stromal Cells in Mice Following Allogeneic T-Cell-Depleted Bone Marrow Transplantation.

机译:同种异体T细胞贫血的骨髓移植后,白介素7转导的骨髓基质细胞对小鼠的抗白血病作用。

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Impaired immune reconstitution following allogeneic bone marrow transplantation (BMT) remains a major obstacle to its clinical application. In this study, interleukin (IL)-7-transduced bone marrow stromal cells (MSC-IL7, 1 x 10(6)/mouse) were transfused into lethally irradiated C57BL/6 recipient mice. By day 40 after transplantation, the recipient mice were challenged with the lymphoma cell line EL4. MSC-IL7 cotransplantation protected recipient mice from leukemic mortality (MST >120 days after BMT vs mean survival time (MST) 70 days in the PBS group) It enhance the PFC count and DTH responses of recipients after transplantation. In conclusion, MSC mediated IL-7 gene therapy and may be a more feasible strategy to restore immune function following allo-TCD-BMT.
机译:同种异体骨髓移植(BMT)后免疫重建受损仍然是其临床应用的主要障碍。在这项研究中,将白介素(IL)-7转导的骨髓基质细胞(MSC-IL7,1 x 10(6)/小鼠)输注经致死剂量照射的C57BL / 6受体小鼠。移植后第40天,用淋巴瘤细胞株EL4攻击受体小鼠。 MSC-IL7共移植可保护受体小鼠免于白血病死亡(BMT后MST> 120天,而PBS组为70天平均存活时间(MST)),可提高移植后受体的PFC计数和DTH反应。总之,MSC介导的IL-7基因治疗可能是在allo-TCD-BMT后恢复免疫功能的更可行策略。

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