心脏移植后的现代免疫抑制剂

MaraviÄ-StojkoviÄ Vera, S. Branislav, PeriÄ Miodrag
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引用次数: 3

摘要

本文的目的是深入了解心脏移植中免疫抑制的当前趋势。目前可用的药物类别:类固醇,抗代谢物,多克隆和单克隆抗体,钙调磷酸酶抑制剂,增殖信号抑制剂已被密切描述。这些药物要么用于预防,要么作为维持免疫抑制方案的一部分。诱导疗法将免疫抑制作为诱导移植物耐受的关键。器官移植受体免疫抑制的骨干:环孢素A和他克莫司联合辅助免疫抑制剂已被广泛应用于维持治疗。我们还提到了正在开发的免疫抑制剂:淋巴细胞调节疗法、耐受性诱导药物、基因治疗的可能性和异种移植作为克服器官短缺的选择。心脏移植后使用免疫抑制药物来降低供体器官排斥的风险。重点是防止移植物排斥,因为宿主免疫系统会攻击可能导致伤害和危及生命的外来抗原。排斥的可能性是永远存在的,这不可避免地要求使用免疫抑制药物,并增加了不必要的副作用的风险。术后并发症包括超急性、急性或慢性排斥反应,以及移植后淋巴增生性疾病,以及对各种感染的永久性易感性。不幸的是,由于侵袭性免疫抑制,一些受者发生肾功能衰竭或恶性疾病。免疫抑制剂不仅作用机制不同,而且副作用也不同。这提供了一个将药物与协同作用结合起来的机会,并有机会成功地定制心脏移植后的抗排斥治疗。
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Modern immunosuppressive agents after heart transplantation
The purpose of this article is to give an insight into current trends of immunosuppression in heart transplantation. Presently available classes of drugs: steroids, antimetabolites, polyclonal and monoclonal antibodies, calcineurin inhibitors, proliferation signal inhibitors have been described closely. These drugs are in use either in a prophylactic manner or as the part of the maintenance immunosuppressive regimen. Induction therapy provides immune suppression as key point to induce graft tolerance. The backbone of immunosuppression in organ transplant recipient: cyclosporine A and tacrolimus have been widely used as maintenance therapy in combination with adjunctive immunosuppressant. We also mentioned the immunosuppressive agents in development: lymphocyte modulation therapy, tolerance induction drugs, gene therapy possibilities and xenotransplantation as option to overcome the organ shortage. After heart transplantation immunosuppressive medications are used to reduce the risk of donor`s organ rejection. The focus is to prevent graft rejection, since host immune system is programmed to attack foreign antigens which could cause injuries and lifethreatening conditions. The possibility of rejection is everlasting, which inevitably demands the use of immunosuppressive drugs and raise the risk of unwanted side effects. Post-operative complications include hyper acute, acute or chronic rejection, as well as post-transplant lymphoprolipherative disorders, and permanent susceptibility to various infections. Unfortunately, some recipients developed the renal failure or malignant diseases due to the aggressive immunosuppression. Immunosuppressant agents differ not only in mechanism of action but also in undesirable side effects. This offers an opportunity to combine drugs with synergistic actions and chance to successfully tailor anti-rejection therapy after heart transplantation.
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