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补体与移植:从新机制到潜在生物标志物及新型治疗策略

Complement and Transplantation: From New Mechanisms to Potential Biomarkers and Novel Treatment Strategies.

作者信息

Horwitz Julian K, Chun Nicholas H, Heeger Peter S

机构信息

Translational Transplant Research Center, Icahn School of Medicine at Mount Sinai, One Gustave L Levy Place, New York, NY 10029, USA; Department of Surgery, Icahn School of Medicine at Mount Sinai, One Gustave L Levy Place, New York, NY 10029, USA.

Translational Transplant Research Center, Icahn School of Medicine at Mount Sinai, One Gustave L Levy Place, New York, NY 10029, USA; Department of Medicine, Icahn School of Medicine at Mount Sinai, One Gustave L Levy Place, New York, NY 10029, USA.

出版信息

Clin Lab Med. 2019 Mar;39(1):31-43. doi: 10.1016/j.cll.2018.10.004. Epub 2018 Dec 20.

DOI:10.1016/j.cll.2018.10.004
PMID:30709507
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6361534/
Abstract

The complement system, traditionally considered a component of innate immunity, is now recognized as a crucial mediator of the adaptive immune response in solid organ transplantation. Preclinical and early human trials have demonstrated the importance of complement effector mechanisms in driving allograft injury during specific antigraft immune responses, including ischemia-reperfusion injury, T-cell-mediated rejection, and antibody-mediated rejection, as well as a potential role for complement-derived risk stratification biomarkers. These data support the need for further testing of complement inhibitors in solid organ transplant recipients.

摘要

补体系统传统上被认为是固有免疫的一个组成部分,现在被公认为实体器官移植中适应性免疫反应的关键调节因子。临床前和早期人体试验已经证明,在特定的抗移植免疫反应中,补体效应机制在驱动同种异体移植物损伤方面具有重要作用,包括缺血再灌注损伤、T细胞介导的排斥反应和抗体介导的排斥反应,以及补体衍生的风险分层生物标志物的潜在作用。这些数据支持在实体器官移植受者中进一步测试补体抑制剂的必要性。

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本文引用的文献

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Association Between Promoter Polymorphisms in CD46 and CD59 in Kidney Donors and Transplant Outcome.供体肾组织中 CD46 和 CD59 启动子多态性与移植结局的关系。
Front Immunol. 2018 May 14;9:972. doi: 10.3389/fimmu.2018.00972. eCollection 2018.
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A phase I/II, double-blind, placebo-controlled study assessing safety and efficacy of C1 esterase inhibitor for prevention of delayed graft function in deceased donor kidney transplant recipients.一项 I/II 期、双盲、安慰剂对照研究,评估 C1 酯酶抑制剂预防尸体供肾移植受者延迟肾功能恢复的安全性和有效性。
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CD55在控制伤口愈合中的关键作用。
J Immunol. 2024 Apr 1;212(7):1142-1149. doi: 10.4049/jimmunol.2300628.
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Complement, complosome, and complotype: A perspective.补体、补体复合物和补体型:一种观点。
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Complement-targeted therapies in kidney transplantation-insights from preclinical studies.补体靶向治疗在肾移植中的研究进展。
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Iguratimod Attenuates Macrophage Polarization and Antibody-Mediated Rejection After Renal Transplant by Regulating KLF4.艾拉莫德通过调控KLF4减轻肾移植后巨噬细胞极化和抗体介导的排斥反应。
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The Evaluation and Validation of Blood-Derived Novel Biomarkers for Precise and Rapid Diagnosis of Tuberculosis in Areas With High-TB Burden.在结核病高负担地区用于结核病精准快速诊断的血液源性新型生物标志物的评估与验证
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More than a Pore: Nonlytic Antimicrobial Functions of Complement and Bacterial Strategies for Evasion.不止一个孔:补体的非裂解性抗菌功能和细菌逃避的策略。
Microbiol Mol Biol Rev. 2021 Jan 27;85(1). doi: 10.1128/MMBR.00177-20. Print 2021 Feb 17.
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A novel injury site-natural antibody targeted complement inhibitor protects against lung transplant injury.一种新型损伤部位-天然抗体靶向补体抑制剂可预防肺移植损伤。
Am J Transplant. 2021 Jun;21(6):2067-2078. doi: 10.1111/ajt.16404. Epub 2021 Feb 26.
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Donor pretreatment with nebulized complement C3a receptor antagonist mitigates brain-death induced immunological injury post-lung transplant.
供体预处理联合雾化补体 C3a 受体拮抗剂减轻肺移植后脑死亡诱导的免疫损伤。
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