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共刺激通路干预作为移植物抗宿主病的治疗方法。

Intervention with costimulatory pathways as a therapeutic approach for graft-versus-host disease.

机构信息

School of Biological Sciences, University of Ulsan, Ulsan 680-749, Korea.

出版信息

Exp Mol Med. 2010 Oct 31;42(10):675-83. doi: 10.3858/emm.2010.42.10.071.


DOI:10.3858/emm.2010.42.10.071
PMID:20820112
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2966741/
Abstract

Graft-versus-host disease (GVHD) is mediated by mature donor T cells contained in the hematopoietic stem cell graft. During the development of GVHD, signaling through a variety of costimulatory receptors plays an important role in allogeneic T cell responses. Even though delivery of costimulatory signals is a prerequisite for full activation of donor T cells in the phase of their interactions with host APCs, their involvement with GVHD might occur over multiple stages. Like many other aspects of GVHD, promise of therapeutic interventions with costimulatory pathways has been gleaned from preclinical models. In this review, I summarize some of the advances in roles of costimulatory molecules in GVHD pathophysiology and discuss preclinical approaches that warrant further exploration in the clinic, focusing on novel strategies to delete pathogenic T cells.

摘要

移植物抗宿主病(GVHD)是由造血干细胞移植中成熟的供体细胞 T 细胞介导的。在 GVHD 的发展过程中,各种共刺激受体的信号转导在同种异体 T 细胞反应中起着重要作用。尽管共刺激信号的传递是供体细胞 T 细胞在与宿主 APC 相互作用阶段完全激活的前提条件,但它们在 GVHD 中的参与可能发生在多个阶段。像 GVHD 的许多其他方面一样,通过临床前模型获得了针对共刺激途径的治疗干预的承诺。在这篇综述中,我总结了共刺激分子在 GVHD 病理生理学中的一些作用,并讨论了值得在临床上进一步探索的临床前方法,重点是删除致病性 T 细胞的新策略。

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引用本文的文献

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Activation of the Nuclear Erythroid 2-Related Factor 2 Antioxidant Responsive Element (Nrf2-ARE) Signaling Pathway Alleviates Acute Graft-Versus-Host Disease by Reducing Oxidative Stress and Inhibiting Infiltration of Inflammatory Cells in an Allogeneic Stem Cell Transplantation Mouse Model.

Med Sci Monit. 2018-8-27

[2]
Host-Derived CD70 Suppresses Murine Graft-versus-Host Disease by Limiting Donor T Cell Expansion and Effector Function.

J Immunol. 2017-7-1

[3]
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Viruses. 2016-3-22

[4]
Acute graft-versus-host disease: are we close to bringing the bench to the bedside?

Best Pract Res Clin Haematol. 2013-10-16

[5]
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Stem Cells Transl Med. 2012-12-19

[6]
Anti-CD137 mAb Deletes Both Donor CD4 and CD8 T Cells in Acute Graft-versus-host Disease.

Immune Netw. 2011-12-31

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[1]
4-1BB ligand as an effective multifunctional immunomodulator and antigen delivery vehicle for the development of therapeutic cancer vaccines.

Cancer Res. 2010-4-20

[2]
Advances in lupus stemming from the parent-into-F1 model.

Trends Immunol. 2010-3-31

[3]
Dendritic cells and Stat3 are essential for CD137-induced CD8 T cell activation-induced cell death.

J Immunol. 2010-3-29

[4]
The safety and side effects of monoclonal antibodies.

Nat Rev Drug Discov. 2010-3-22

[5]
CD137-CD137 Ligand Interactions in Inflammation.

Immune Netw. 2009-6-30

[6]
CD137 agonist antibody prevents cancer recurrence: contribution of CD137 on both hematopoietic and nonhematopoietic cells.

Blood. 2010-1-12

[7]
Costimulatory pathways in transplantation: challenges and new developments.

Immunol Rev. 2009-5

[8]
Mechanisms of costimulation.

Immunol Rev. 2009-5

[9]
The role of TNF superfamily members in T-cell function and diseases.

Nat Rev Immunol. 2009-4

[10]
4-1BB functions as a survival factor in dendritic cells.

J Immunol. 2009-4-1

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