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首页> 外文期刊>Comparative Medicine >Physiologic Aspects of Pig Kidney Transplantation in Nonhuman Primates
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Physiologic Aspects of Pig Kidney Transplantation in Nonhuman Primates

机译:非人印象猪肾移植的生理方面

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Xenotransplantation can provide a solution to the current shortage of human organs for patients with terminal renal failure. The increasing availability of genetically engineered pigs, effective immunosuppressive therapy, and antiinflammatory therapy help to protect pig tissues from the primate immune response and can correct molecular incompatibilities. Life-supporting pig kidney xenografts have survived in NHP for more than 6 mo in the absence of markers of consumptive coagulopathy. However, few reports have focused on the physiologic aspects of life-supporting pig kidney xenografts. We have reviewed the literature regarding pig kidney xenotransplantation in NHP. The available data indicate (1) normal serum creatinine, (2) normal serum electrolytes, except for a trend toward increased calcium levels and a transient rise in phosphate followed by a fall to slightly subnormal values, (3) minimal or modest proteinuria without hypoalbuminemia (suggesting that previous reports of proteinuria likely were due to a low-grade immune response rather than physiologic incompatibilities), (4) possible discrepancies between pig erythropoietin and the primate erythropoietin receptor, and (5) significant early increase in kidney graft size, which might result from persistent effects of pig growth hormone. Further study is required regarding identification and investigation of physiologic incompatibilities. However, current evidence suggests that, in the absence of an immune response, a transplanted pig kidney likely would satisfactorily support a human patient.
机译:异种持续物可以为终末肾功能衰竭患者提供目前人体器官短缺的解决方案。遗传工程猪的可用性越来越多,有效的免疫抑制治疗和抗炎治疗有助于保护猪组织免受灵长类动物免疫应答,可以纠正分子不相容。在没有消毒凝血病的标记的情况下,寿命支持的猪肾异种移植物在NHP避免了超过6月。然而,很少有报道集中在生命支持的猪肾异种移植物的生理方面。我们已经审查了关于NHP猪肾蛋白化的文献。可用数据表明(1)正常血清肌酐,(2)正常血清电解质,除了增加钙水平的趋势,磷酸盐瞬态升高,然后落到略微亚核值,(3)没有低聚抑制症的最小或适度的蛋白尿(暗示蛋白尿的先前报告可能是由于低级别的免疫反应而不是生理的不兼容性),(4)猪促红细胞生成素和灵长类动物促红细胞生成素受体之间可能的差异,以及(5)肾移植大小的显着提高可能是由于猪生长激素的持续影响。需要进一步研究,关于身份证明和对生理学不相容性的调查。然而,目前的证据表明,在没有免疫应答的情况下,移植的猪肾可能会令人满意地支持人类患者。

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