abo血型不相容的肾移植:从生理盐水冲洗到抗原特异性免疫吸附-克服屏障的工具。

The Korean Journal of Hematology Pub Date : 2011-09-01 Epub Date: 2011-09-30 DOI:10.5045/kjh.2011.46.3.164
Mario Schiffer, Jan T Kielstein
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引用次数: 10

摘要

1951年4月23日,一位30岁的女性在波士顿接受了首例ABO血型不相容肾移植手术。当时,人们普遍认为强烈冲洗移植物以清除血液足以克服与血型不相容相关的任何免疫问题。然而,当上述患者和另一位ABOi移植受者在一个月内死亡时,Humes及其同事得出了同样的结论:“我们不认为存在血液不相容的肾移植是明智的。”在随后的几十年里,我们了解到代表abo血型抗原的寡糖表面抗原不仅在红细胞上表达,而且在包括血管内皮在内的各种组织的细胞上表达。器官需求和可获得性之间日益扩大的差距促使人们努力克服ABO障碍。在经历了20世纪70年代早期令人失望的结果之后,日本在20世纪80年代成为这一努力的领导者。所有方案都基于两种策略:用体外技术去除预先形成的抗体和抑制正在产生的抗体。随着脾切除术、新的免疫抑制药物(如利妥昔单抗,一种抗CD20的单克隆抗体)和抗原特异性免疫吸附等体外方法的出现,ABOi肾移植的成功成为可能。本文综述了ABOi移植的潜在病理生理学和不同的可行方案。此外,我们简要地探讨了潜在的短期和长期问题,特别是感染并发症和恶性肿瘤的发生率,这可能与高强度免疫抑制治疗有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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ABO-incompatible renal transplantation: From saline flushes to antigen-specific immunoadsorption-Tools to overcome the barrier.

On April 23, 1951, a 30-year-old woman received the first intentional ABOi (ABO incompatible) renal transplantation in Boston. At that time, it was commonly believed that intensely rinsing the graft to remove blood would be sufficient to overcome any immunological problems associated with blood type incompatibility. However, when the abovementioned patient and another ABOi transplant recipient died within a month, Humes and colleagues arrived at the same conclusion: "We do not feel that renal transplantation in the presence of blood incompatibility is wise." In the decades that followed, we learned that the oligosaccharide surface antigens representing the ABO-blood group antigens are expressed not only on erythrocytes but also on cells from various tissues, including the vascular endothelium. The growing gap between organ demand and availability has sparked efforts to overcome the ABO barrier. After its disappointing results in the early 1970s, Japan became the leader of this endeavor in the 1980s. All protocols are based on 2 strategies: removal of preformed antibodies with extracorporeal techniques and inhibition of ongoing antibody production. Successful ABOi renal transplantation became possible with the advent of splenectomy, new immunosuppressive drugs (e.g., rituximab, a monoclonal antibody against CD20), and extracorporeal methods such as antigen-specific immunoadsorption. This review summarizes the underlying pathophysiology of ABOi transplantation and the different protocols available. Further, we briefly touch potential short- and long-term problems, particularly the incidence of infectious complications and malignancies, that can arise with high-intensity immunosuppressive therapy.

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