首页> 外文期刊>Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation >Induction of lethal graft-versus-host disease by anti-CD137 monoclonal antibody in mice prone to chronic graft-versus-host disease.
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Induction of lethal graft-versus-host disease by anti-CD137 monoclonal antibody in mice prone to chronic graft-versus-host disease.

机译:抗CD137单克隆抗体在易患慢性移植物抗宿主病的小鼠中诱导致死性移植物抗宿主病。

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Chronic graft-versus-host disease (cGVHD) is an increasingly frequent complication of allogeneic stem cell transplantation. We previously showed that anti-CD137 monoclonal antibody (mAb) can cure advanced cGVHD by inducing activation-induced cell death of donor T cells. In this study, we examined whether administration of anti-CD137 mAb can prevent the development of cGVHD after bone marrow transplantation (BMT) in mice conditioned with total body irradiation (TBI). We used the B10.D2-->Balb/c (H-2(d)) minor histocompatibility antigen-mismatched model, which reflects clinical and pathological symptoms of human cGVHD. A single injection of anti-CD137 mAb was administered immediately after BMT. In contrast to the results obtained from the curing model of cGVHD, anti-CD137 given simultaneously with BMT resulted in lethal GVHD. Histopathologic evaluation revealed inflammation and damage of target organs from acute GVHD (aGVHD) in anti-CD137-treated mice. Anti-CD137-induced lethal aGVHD required host cells,as well as irradiation and mature donor T cells. Apparently, anti-CD137 mAb rapidly induced activation of donor T cells and sustained their activation status under the inflammatory condition triggered by irradiation. When given on day 12 after irradiation and BMT, anti-CD137 mAb could still exacerbate GVHD, but when given on day 30, it could not. Our data demonstrate that anti-CD137 mAb can amplify inflammation induced by host preconditioning, subsequently resulting in lethal aGVHD; thus, alleviating irradiation-induced toxicity is critical to allow the use of anti-CD137 mAb as GVHD prophylaxis.
机译:慢性移植物抗宿主病(cGVHD)是同种异体干细胞移植中越来越常见的并发症。我们以前显示抗CD137单克隆抗体(mAb)可以通过诱导供体T细胞活化诱导的细胞死亡来治愈晚期cGVHD。在这项研究中,我们检查了抗CD137 mAb的使用是否可以预防全身照射(TBI)的小鼠骨髓移植(BMT)后cGVHD的发展。我们使用了B10.D2-> Balb / c(H-2(d))次要组织相容性抗原不匹配模型,该模型反映了人类cGVHD的临床和病理症状。 BMT之后立即单次注射抗CD137 mAb。与从cGVHD治愈模型获得的结果相反,与BMT同时给予的抗CD137导致致命的GVHD。组织病理学评估显示,抗CD137处理的小鼠急性GVHD(aGVHD)引起炎症和靶器官损伤。抗CD137诱导的致死性aGVHD需要宿主细胞,以及辐射和成熟的供体T细胞。显然,抗CD137 mAb迅速诱导了供体T细胞的活化,并在辐射触发的炎症条件下维持了它们的活化状态。在放疗和BMT后第12天给予抗CD137 mAb仍可加重GVHD,但在第30天给予抗CD137 mAb则不能。我们的数据表明,抗CD137 mAb可以放大宿主预处理引起的炎症,从而导致致命的aGVHD。因此,减轻辐射诱导的毒性对于允许使用抗CD137 mAb作为预防GVHD至关重要。

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