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经氨甲蝶呤处理的供体T细胞在异基因骨髓移植后具有多克隆抗原特异性长期功能且无移植物抗宿主病。

Amotosalen-treated donor T cells have polyclonal antigen-specific long-term function without graft-versus-host disease after allogeneic bone marrow transplantation.

作者信息

Hossain Mohammad Sohrab, Roback John D, Lezhava Levan, Hillyer Christopher D, Waller Edmund K

机构信息

Department of Hematology and Oncology, Division of Stem Cell and Bone Marrow Transplantation, Winship Cancer Institute, Emory Universiy School of Medicine, Atlanta, Georgia, USA.

出版信息

Biol Blood Marrow Transplant. 2005 Mar;11(3):169-80. doi: 10.1016/j.bbmt.2004.12.332.

Abstract

We have previously shown that amotosalen HCl (S-59 psoralen)-treated donor splenocytes, which have limited proliferative capacity in vitro, can protect major histocompatibility complex-mismatched bone marrow transplant (BMT) recipients from lethal murine cytomegalovirus infection without causing graft-versus-host disease. In this study, we further investigated the effects of amotosalen-treated donor T cells on immune reconstitution after allogeneic BMT. We were surprised to find that amotosalen-treated donor T cells persisted long-term in vivo, comprising 6% to 10% on average of the T-cell compartment of transplant recipients at 4 months after transplantation. Donor T cells derived from amotosalen-treated splenocytes were predominantly polyclonal CD44 hi/int CD8 + memory T cells and were functionally active, synthesizing interferon gamma in response to stimulation with murine cytomegalovirus antigen. Amotosalen-treated donor T cells, reisolated from BMT recipients' spleens >/=4 months after transplantation, proliferated in vitro, thus indicating repair of amotosalen-mediated DNA cross-links. Compared with infusion of untreated donor splenocytes, amotosalen-treated cells enhanced thymopoiesis by bone marrow-derived stem cells in BMT recipients. However, amotosalen treatment abrogated the thymopoietic activity of lymphoid progenitor cells among the donor splenocytes. Thus, infusion of amotosalen-treated donor T cells produced rapid immune reconstitution after major histocompatibility complex-mismatched BMT by transferring long-lived polyclonal memory T cells with antiviral activity and also by enhancing bone marrow-derived thymopoiesis. This is a novel approach to adoptive immunotherapy in allogeneic BMT.

摘要

我们之前已经表明,盐酸氨莫司汀(S-59补骨脂素)处理的供体脾细胞在体外增殖能力有限,但可保护主要组织相容性复合体不匹配的骨髓移植(BMT)受者免受致命的鼠巨细胞病毒感染,且不会引发移植物抗宿主病。在本研究中,我们进一步研究了氨莫司汀处理的供体T细胞对异基因BMT后免疫重建的影响。我们惊讶地发现,氨莫司汀处理的供体T细胞在体内长期存在,移植后4个月时平均占移植受者T细胞区室的6%至10%。源自氨莫司汀处理的脾细胞的供体T细胞主要是多克隆CD44高/中CD8 +记忆T细胞,并且功能活跃,在受到鼠巨细胞病毒抗原刺激时可合成γ干扰素。从移植后≥4个月的BMT受者脾脏中重新分离出的氨莫司汀处理的供体T细胞在体外增殖,这表明氨莫司汀介导的DNA交联得到修复。与输注未处理的供体脾细胞相比,氨莫司汀处理的细胞增强了BMT受者中骨髓来源干细胞的胸腺生成。然而,氨莫司汀处理消除了供体脾细胞中淋巴祖细胞的胸腺生成活性。因此,输注氨莫司汀处理的供体T细胞通过转移具有抗病毒活性的长寿多克隆记忆T细胞以及增强骨髓来源的胸腺生成,在主要组织相容性复合体不匹配的BMT后产生了快速的免疫重建。这是异基因BMT中过继性免疫治疗的一种新方法。

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