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移植物抗宿主病的小鼠模型:进展与局限性。

Mouse models of graft-versus-host disease: advances and limitations.

机构信息

Division of Oncology, Siteman Cancer Center, Washington University School of Medicine, St Louis, MO 63110, USA.

出版信息

Dis Model Mech. 2011 May;4(3):318-33. doi: 10.1242/dmm.006668.

Abstract

The limiting factor for successful hematopoietic stem cell transplantation (HSCT) is graft-versus-host disease (GvHD), a post-transplant disorder that results from immune-mediated attack of recipient tissue by donor T cells contained in the transplant. Mouse models of GvHD have provided important insights into the pathophysiology of this disease, which have helped to improve the success rate of HSCT in humans. The kinetics with which GvHD develops distinguishes acute from chronic GvHD, and it is clear from studies of mouse models of GvHD (and studies of human HSCT) that the pathophysiology of these two forms is also distinct. Mouse models also further the basic understanding of the immunological responses involved in GvHD pathology, such as antigen recognition and presentation, the involvement of the thymus and immune reconstitution after transplantation. In this Perspective, we provide an overview of currently available mouse models of acute and chronic GvHD, highlighting their benefits and limitations, and discuss research and clinical opportunities for the future.

摘要

造血干细胞移植(HSCT)成功的限制因素是移植物抗宿主病(GvHD),这是一种移植后疾病,由移植中供体 T 细胞介导的免疫攻击受体组织引起。GvHD 的小鼠模型为该疾病的病理生理学提供了重要的见解,这有助于提高人类 HSCT 的成功率。GvHD 发展的动力学将其区分为急性和慢性 GvHD,从 GvHD 的小鼠模型研究(和人类 HSCT 研究)中可以清楚地看出,这两种形式的病理生理学也不同。小鼠模型还进一步加深了对 GvHD 病理涉及的免疫反应的基本理解,例如抗原识别和呈递、胸腺的参与以及移植后的免疫重建。在本观点中,我们概述了目前可用的急性和慢性 GvHD 小鼠模型,强调了它们的优点和局限性,并讨论了未来的研究和临床机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea72/3097454/c51d1ba4f737/DMM006668F1.jpg

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