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Nonhuman primate infections after organ transplantation

机译:器官移植后的非人类灵长类动物感染

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Nonhuman primates, primarily rhesus macaques (Macaca mulatta), cynomolgus macaques (Macaca fascicularis), and baboons (Papio spp.), have been used extensively in research models of solid organ transplantation, mainly because the nonhuman primate (NHP) immune system closely resembles that of the human. Nonhuman primates are also frequently the model of choice for preclinical testing of new immunosuppressive strategies. But the management of post-transplant nonhuman primates is complex, because it often involves multiple immunosuppressive agents, many of which are new and have unknown effects. Additionally, the resulting immunosuppression carries a risk of infectious complications, which are challenging to diagnose. Last, because of the natural tendency of animals to hide signs of weakness, infectious complications may not be obvious until the animal becomes severely ill. For these reasons the diagnosis of infectious complications is difficult among post-transplant NHPs. Because most nonhuman primate studies in organ transplantation are quite small, there are only a few published reports concerning infections after transplantation in nonhuman primates. Based on our survey of these reports, the incidence of infection in NHP transplant models is 14%. The majority of reports suggest that many of these infections are due to reactivation of viruses endemic to the primate species, such as cytomegalovirus (CMV), polyomavirus, and Epstein-Barr virus (EBV)-related infections. In this review, we address the epidemiology, pathogenesis, role of prophylaxis, clinical presentation, and treatment of infectious complications after solid organ transplantation in nonhuman primates.
机译:非人类灵长类动物,主要是恒河猴(Macaca mulatta),食蟹猕猴(Macaca fascicularis)和狒狒(Papio spp。),已广泛用于实体器官移植的研究模型中,这主要是因为非人类灵长类动物(NHP)免疫系统非常相似人类的。非人类的灵长类动物通常也是新的免疫抑制策略的临床前测试的选择模型。但是移植后非人类灵长类动物的管理很复杂,因为它经常涉及多种免疫抑制剂,其中许多是新的并且具有未知的作用。另外,所产生的免疫抑制具有感染并发症的风险,这对诊断具有挑战性。最后,由于动物自然会隐藏无力的迹象,因此直到动物患上重病之前,感染性并发症才变得明显。由于这些原因,在移植后的NHP中很难诊断出感染性并发症。由于大多数非人类灵长类动物在器官移植中的研究都很少,因此,关于非人类灵长类动物移植后感染的报道很少。根据我们对这些报告的调查,NHP移植模型中的感染发生率为14%。大多数报告表明,其中许多感染是由于重新激活了灵长类物种特有的病毒,例如巨细胞病毒(CMV),多瘤病毒和爱泼斯坦-巴尔病毒(EBV)相关的感染。在这篇综述中,我们探讨了非人类灵长类动物实体器官移植后的流行病学,发病机制,预防作用,临床表现和感染并发症的治疗。

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