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10
Graft-implanted, enzyme responsive, tacrolimus-eluting hydrogel enables long-term survival of orthotopic porcine limb vascularized composite allografts: A proof of concept study.移植物植入、酶响应、他克莫司洗脱水凝胶使原位猪肢体血管化复合同种异体移植物长期存活:概念验证研究。
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本文引用的文献

1
Immunological issues in clinical composite tissue allotransplantation: where do we stand today?临床复合组织同种异体移植中的免疫学问题:我们今天处于什么位置?
Transplantation. 2012 May 15;93(9):855-9. doi: 10.1097/TP.0b013e31824728b8.
2
Face transplantation: outcomes, concerns, controversies, and future directions.面部移植:结果、关注点、争议及未来方向。
J Craniofac Surg. 2012 Jan;23(1):254-9. doi: 10.1097/SCS.0b013e318241b920.
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Facial angiofibromas treated with topical rapamycin: an excellent choice with fast response.外用雷帕霉素治疗面部血管纤维瘤:快速起效的极佳选择。
Dermatol Online J. 2012 Jan 15;18(1):15.
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Pimecrolimus 1% cream for the treatment of seborrheic dermatitis: a systematic review of randomized controlled trials.吡美莫司乳膏治疗脂溢性皮炎:随机对照试验的系统评价。
Expert Rev Clin Pharmacol. 2012 Jan;5(1):91-7. doi: 10.1586/ecp.11.68.
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An update on facial transplantation cases performed between 2005 and 2010.2005 年至 2010 年期间进行的面部移植案例更新。
Plast Reconstr Surg. 2011 Dec;128(6):707e-720e. doi: 10.1097/PRS.0b013e318230c77b.
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Favoring the risk-benefit balance for upper extremity transplantation--the Pittsburgh Protocol.支持上肢移植的风险效益平衡——匹兹堡方案
Hand Clin. 2011 Nov;27(4):511-20, ix-x. doi: 10.1016/j.hcl.2011.08.008.
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Pimecrolimus 1% cream for oral erosive lichen planus: a 6-week randomized, double-blind, vehicle-controlled study with a 6-week open-label extension to assess efficacy and safety.他克莫司乳膏 1%治疗口腔糜烂性扁平苔藓:6 周随机、双盲、安慰剂对照研究,6 周开放性扩展研究以评估疗效和安全性。
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The skin is the body's largest organ.
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Molecular markers and targeted therapy of skin rejection in composite tissue allotransplantation.复合组织同种异体移植中皮肤排斥的分子标志物和靶向治疗。
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血管化复合组织移植中的位点特异性免疫抑制:前景与潜力

Site-specific immunosuppression in vascularized composite allotransplantation: prospects and potential.

作者信息

Schnider Jonas T, Weinstock Matthias, Plock Jan A, Solari Mario G, Venkataramanan Raman, Zheng Xin Xiao, Gorantla Vijay S

机构信息

Department of Plastic and Reconstructive Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.

出版信息

Clin Dev Immunol. 2013;2013:495212. doi: 10.1155/2013/495212. Epub 2013 Feb 13.

DOI:10.1155/2013/495212
PMID:23476677
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3586464/
Abstract

Skin is the most immunogenic component of a vascularized composite allograft (VCA) and is the primary trigger and target of rejection. The skin is directly accessible for visual monitoring of acute rejection (AR) and for directed biopsy, timely therapeutic intervention, and management of AR. Logically, antirejection drugs, biologics, or other agents delivered locally to the VCA may reduce the need for systemic immunosuppression with its adverse effects. Topical FK 506 (tacrolimus) and steroids have been used in clinical VCA as an adjunct to systemic therapy with unclear beneficial effects. However, there are no commercially available topical formulations for other widely used systemic immunosuppressive drugs such as mycophenolic acid, sirolimus, and everolimus. Investigating the site-specific therapeutic effects and efficacy of systemically active agents may enable optimizing the dosing, frequency, and duration of overall immunosuppression in VCA with minimization or elimination of long-term drug-related toxicity.

摘要

皮肤是血管化复合组织异体移植(VCA)中免疫原性最强的成分,是排斥反应的主要触发因素和靶点。皮肤便于直接进行急性排斥反应(AR)的视觉监测以及定向活检、及时的治疗干预和AR的管理。从逻辑上讲,局部递送至VCA的抗排斥药物、生物制剂或其他药物可能会减少全身性免疫抑制及其不良反应的需求。局部用FK 506(他克莫司)和类固醇已在临床VCA中用作全身治疗的辅助药物,但其有益效果尚不清楚。然而,对于其他广泛使用的全身性免疫抑制药物,如霉酚酸、西罗莫司和依维莫司,尚无市售的局部制剂。研究全身活性药物的位点特异性治疗效果和疗效,可能有助于优化VCA中整体免疫抑制的剂量、频率和持续时间,同时将长期药物相关毒性降至最低或消除。