Literature DB >> 10961298

Productive infection of primary human endothelial cells by pig endogenous retrovirus (PERV).

U Martin1, M E Winkler, M Id, H Radeke, L Arseniev, Y Takeuchi, A R Simon, C Patience, A Haverich, G Steinhoff.   

Abstract

The potential risk of viral transmission in the setting of xenotransplantation has gained major attention. Different porcine cell types have been shown to release retroviral particles, which are infectious for human cell lines in vitro. However, there are only a few data on whether PERV (pig endogenous retrovirus) is able to infect primary human cells. In this study we have analyzed endothelial cells, vascular fibroblasts, mesangial cells, mononuclear cells, hematopoetic stem cells and bone marrow stromal cells for PERV transmission. We now provide evidence for primary human endothelial cells, vascular fibroblasts, and mesangial cells to be susceptible to PERV transmission. PERV infection was productive in endothelial cells and mesangial cells. Our data confirm and extend former reports concerning the PERV infection of human cells. The PERV infection of different primary human cells represents further significant evidence for a viral risk during xenotransplantation. In this context, special attention should be directed towards productive infection of human endothelial cells: in the setting of xenotransplantation this cell type will have close contact with porcine cells and PERV particles.

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Year:  2000        PMID: 10961298     DOI: 10.1034/j.1399-3089.2000.00052.x

Source DB:  PubMed          Journal:  Xenotransplantation        ISSN: 0908-665X            Impact factor:   3.907


  31 in total

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Journal:  J Virol       Date:  2001-12       Impact factor: 5.103

5.  Infection of nonhuman primate cells by pig endogenous retrovirus.

Authors:  J H Blusch; C Patience; Y Takeuchi; C Templin; C Roos; K Von Der Helm; G Steinhoff; U Martin
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6.  Treatment of fulminant hepatic failure in rats using a bioartificial liver device containing porcine hepatocytes producing interleukin-1 receptor antagonist.

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7.  Absence of replication of porcine endogenous retrovirus and porcine lymphotropic herpesvirus type 1 with prolonged pig cell microchimerism after pig-to-baboon xenotransplantation.

Authors:  Nicolas C Issa; Robert A Wilkinson; Adam Griesemer; David K C Cooper; Kazuhiko Yamada; David H Sachs; Jay A Fishman
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8.  Mice transgenic for a human porcine endogenous retrovirus receptor are susceptible to productive viral infection.

Authors:  Y Martina; K T Marcucci; S Cherqui; A Szabo; T Drysdale; U Srinivisan; C A Wilson; C Patience; D R Salomon
Journal:  J Virol       Date:  2006-04       Impact factor: 5.103

9.  Functional hierarchy of two L domains in porcine endogenous retrovirus (PERV) that influence release and infectivity.

Authors:  Katherine T Marcucci; Yuri Martina; Frank Harrison; Carolyn A Wilson; Daniel R Salomon
Journal:  Virology       Date:  2008-03-19       Impact factor: 3.616

10.  Identification of receptors for pig endogenous retrovirus.

Authors:  Thomas A Ericsson; Yasuhiro Takeuchi; Christian Templin; Gary Quinn; Shelli F Farhadian; James C Wood; Beth A Oldmixon; Kristen M Suling; Jennifer K Ishii; Yoshinori Kitagawa; Takayuki Miyazawa; Daniel R Salomon; Robin A Weiss; Clive Patience
Journal:  Proc Natl Acad Sci U S A       Date:  2003-05-09       Impact factor: 11.205

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