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Infection barriers to successful xenotransplantation focusing on porcine endogenous retroviruses.针对猪内源性逆转录病毒的成功异种移植的感染屏障。
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2
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Cardiac Xenotransplantation: a New Frontier for Advanced Heart Failure.心脏异种移植:晚期心力衰竭的新前沿。
Curr Treat Options Cardiovasc Med. 2023 Mar;25(3):65-78. doi: 10.1007/s11936-023-00977-6. Epub 2023 Feb 8.

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Extracorporeal ("ex vivo") connection of pig kidneys to humans. I. Clinical data and studies of platelet destruction.猪肾脏的体外(“离体”)连接到人体。I. 血小板破坏的临床数据和研究。
Xenotransplantation. 1996 Nov;3(4):328-39. doi: 10.1111/j.1399-3089.1996.tb00155.x.
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Clinical xenotransplantation: the next medical revolution?临床异种移植:下一场医学革命?
Lancet. 2012 Feb 18;379(9816):672-83. doi: 10.1016/S0140-6736(11)61091-X. Epub 2011 Oct 20.
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Influenza A viruses: new research developments.甲型流感病毒:新的研究进展。
Nat Rev Microbiol. 2011 Jul 11;9(8):590-603. doi: 10.1038/nrmicro2613.
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National, regional, and global trends in fasting plasma glucose and diabetes prevalence since 1980: systematic analysis of health examination surveys and epidemiological studies with 370 country-years and 2·7 million participants.1980 年以来,空腹血糖和糖尿病患病率的国家、地区和全球趋势:对 370 个国家和地区年以及 270 万参与者的健康检查调查和流行病学研究的系统分析。
Lancet. 2011 Jul 2;378(9785):31-40. doi: 10.1016/S0140-6736(11)60679-X. Epub 2011 Jun 24.
5
The left half of the XMRV retrovirus is present in an endogenous retrovirus of NIH/3T3 Swiss mouse cells.XMRV 逆转录病毒的左半部分存在于 NIH/3T3 瑞士鼠细胞的内源性逆转录病毒中。
J Virol. 2011 Sep;85(17):9247-8. doi: 10.1128/JVI.05137-11. Epub 2011 Jun 22.
6
Infectious risk in xenotransplantation--what post-transplant screening for the human recipient?异种移植中的感染风险——人类受者在移植后需要进行哪些筛查?
Xenotransplantation. 2011 May-Jun;18(3):151-7. doi: 10.1111/j.1399-3089.2011.00636.x.
7
Recombinant origin of the retrovirus XMRV.逆转录病毒 XMRV 的重组起源。
Science. 2011 Jul 1;333(6038):97-101. doi: 10.1126/science.1205292. Epub 2011 May 31.
8
Initial in vitro investigation of the human immune response to corneal cells from genetically engineered pigs.初步的体外研究人类对基因工程猪角膜细胞的免疫反应。
Invest Ophthalmol Vis Sci. 2011 Jul 15;52(8):5278-86. doi: 10.1167/iovs.10-6947.
9
Multiplex high resolution melting assay for estimation of Porcine Endogenous Retrovirus (PERV) relative gene dosage in pigs and detection of PERV infection in xenograft recipients.用于估计猪内源性逆转录病毒(PERV)相对基因剂量和检测异种移植受者中 PERV 感染的多重高分辨率熔解分析。
J Virol Methods. 2011 Jul;175(1):95-100. doi: 10.1016/j.jviromet.2011.04.026. Epub 2011 Apr 28.
10
Absence of XMRV retrovirus and other murine leukemia virus-related viruses in patients with chronic fatigue syndrome.慢性疲劳综合征患者中不存在 XMRV 逆转录病毒和其他与鼠类白血病病毒相关的病毒。
J Virol. 2011 Jul;85(14):7195-202. doi: 10.1128/JVI.00693-11. Epub 2011 May 4.

针对猪内源性逆转录病毒的成功异种移植的感染屏障。

Infection barriers to successful xenotransplantation focusing on porcine endogenous retroviruses.

机构信息

Robert Koch Institut, Berlin, Germany.

出版信息

Clin Microbiol Rev. 2012 Apr;25(2):318-43. doi: 10.1128/CMR.05011-11.

DOI:10.1128/CMR.05011-11
PMID:22491774
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3346299/
Abstract

Xenotransplantation may be a solution to overcome the shortage of organs for the treatment of patients with organ failure, but it may be associated with the transmission of porcine microorganisms and the development of xenozoonoses. Whereas most microorganisms may be eliminated by pathogen-free breeding of the donor animals, porcine endogenous retroviruses (PERVs) cannot be eliminated, since these are integrated into the genomes of all pigs. Human-tropic PERV-A and -B are present in all pigs and are able to infect human cells. Infection of ecotropic PERV-C is limited to pig cells. PERVs may adapt to host cells by varying the number of LTR-binding transcription factor binding sites. Like all retroviruses, they may induce tumors and/or immunodeficiencies. To date, all experimental, preclinical, and clinical xenotransplantations using pig cells, tissues, and organs have not shown transmission of PERV. Highly sensitive and specific methods have been developed to analyze the PERV status of donor pigs and to monitor recipients for PERV infection. Strategies have been developed to prevent PERV transmission, including selection of PERV-C-negative, low-producer pigs, generation of an effective vaccine, selection of effective antiretrovirals, and generation of animals transgenic for a PERV-specific short hairpin RNA inhibiting PERV expression by RNA interference.

摘要

异种移植可能是解决器官短缺问题、治疗器官衰竭患者的一种方法,但它可能会导致猪微生物的传播和人畜共患病的发生。虽然大多数微生物可以通过对供体动物进行无病原体繁殖来消除,但猪内源性逆转录病毒(PERV)是无法消除的,因为这些病毒已经整合到所有猪的基因组中。所有猪都存在能够感染人类细胞的人嗜性 PERV-A 和 -B,而 ecotropic PERV-C 的感染仅限于猪细胞。PERV 可以通过改变 LTR 结合转录因子结合位点的数量来适应宿主细胞。与所有逆转录病毒一样,它们可能会诱导肿瘤和/或免疫缺陷。迄今为止,所有使用猪细胞、组织和器官的实验、临床前和临床异种移植均未显示 PERV 的传播。已经开发出高度敏感和特异性的方法来分析供体猪的 PERV 状态,并监测受者的 PERV 感染情况。已经制定了预防 PERV 传播的策略,包括选择 PERV-C 阴性、低产生猪、生成有效的疫苗、选择有效的抗逆转录病毒药物,以及生成针对 PERV 特异性短发夹 RNA 的转基因动物,通过 RNA 干扰抑制 PERV 表达。