Hossain Mohammad Sohrab, Roback John D, Lezhava Levan, Hillyer Christopher D, Waller Edmund K
Department of Hematology and Oncology, Division of Stem Cell and Bone Marrow Transplantation, Winship Cancer Institute, Emory Universiy School of Medicine, Atlanta, Georgia, USA.
Biol Blood Marrow Transplant. 2005 Mar;11(3):169-80. doi: 10.1016/j.bbmt.2004.12.332.
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.
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。