Schnider Jonas T, Weinstock Matthias, Plock Jan A, Solari Mario G, Venkataramanan Raman, Zheng Xin Xiao, Gorantla Vijay S
Department of Plastic and Reconstructive Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.
Clin Dev Immunol. 2013;2013:495212. doi: 10.1155/2013/495212. Epub 2013 Feb 13.
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.
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。