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Journal ArticleDOI

Xenotransplantation and pig endogenous retroviruses.

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TLDR
The lack of PERV infection in xenograft recipients up to now is encouraging, but more basic research and controlled animal studies that mimic the pig to human xenotransplantation setting more closely are required for safety assessment.
Abstract
Xenotransplantation, in particular transplantation of pig cells, tissues and organs into human patients, may alleviate the current shortage of suitable allografts available for human transplantation. This overview addresses the physiological, immunological and virological factors considered with regard to xenotransplantation. Among the issues reviewed are the merits of using pigs as xenograft source species, the compatibility of pig and human organ physiology and the immunological hindrances with regard to the various types of rejection and attempts at abrogating rejection. Advances in the prevention of pig organ rejection by creating genetically modified pigs that are more suited to the human microenvironment are also discussed. Finally, with regard to virology, possible zoonotic infections emanating from pigs are reviewed, with special emphasis on the pig endogenous retrovirus (PERV). An in depth account of PERV studies, comprising their discovery as well as recent knowledge of the virus, is given. To date, all retrospective studies on patients with pig xenografts have shown no evidence of PERV transmission, however, many factors make us interpret these results with caution. Although the lack of PERV infection in xenograft recipients up to now is encouraging, more basic research and controlled animal studies that mimic the pig to human xenotransplantation setting more closely are required for safety assessment.

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The discovery of endogenous retroviruses

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Association of human endogenous retroviruses with multiple sclerosis and possible interactions with herpes viruses

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Evolution of carbohydrate antigens—microbial forces shaping host glycomes?

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References
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Journal ArticleDOI

Cloned pigs produced by nuclear transfer from adult somatic cells

TL;DR: The successful production of cloned piglets from a cultured adult somatic cell population using a new nuclear transfer procedure is reported and the methodology used for embryo reconstruction in each of these species is essentially similar.
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Production of α-1,3-Galactosyltransferase Knockout Pigs by Nuclear Transfer Cloning

TL;DR: The production of four live pigs in which one allele of the α-1,3-galactosyltransferase locus has been knocked out is reported, paving the way for xenotransplantation of pigs from clonal fetal fibroblast cell lines.
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Infection of human cells by an endogenous retrovirus of pigs

TL;DR: Kidney, heart and spleen tissue obtained from domestic pigs contained multiple copies of integrated PERV genomes and expressed viral RNA, which could rescue a Moloney retroviral vector and acquired resistance to lysis by human complement.
Journal ArticleDOI

A novel virus in swine is closely related to the human hepatitis E virus

TL;DR: The discovery of swine HEV not only has implications for HEV vaccine development, diagnosis, and biology, but also raises a potential public health concern for zoonosis or xenozoonosis following xenotransplantation with pig organs.
Journal ArticleDOI

Production of α1,3-Galactosyltransferase-Deficient Pigs

TL;DR: The piglets carrying a point mutation in the α1,3GT gene hold significant value, as they would allow production of α1-3Gal-deficient pigs free of antibiotic-resistance genes and thus have the potential to make a safer product for human use.
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