Literature DB >> 11349732

Lack of cross-species transmission of porcine endogenous retrovirus infection to nonhuman primate recipients of porcine cells, tissues, or organs.

W M Switzer1, R E Michler, V Shanmugam, A Matthews, A I Hussain, A Wright, P Sandstrom, L E Chapman, C Weber, S Safley, R R Denny, A Navarro, V Evans, A J Norin, P Kwiatkowski, W Heneine.   

Abstract

BACKGROUND: Nonhuman primates (NHPs) have been widely used in different porcine xenograft procedures inevitably resulting in exposure to porcine endogenous retrovirus (PERV). Surveillance for PERV infection in these NHPs may provide information on the risks of cross-species transmission of PERV, particularly for recipients of vascularized organ xenografts for whom data from human clinical trials is unavailable.
METHODS: We tested 21 Old World and 2 New World primates exposed to a variety of porcine xenografts for evidence of PERV infection. These NHPs included six baboon recipients of pig hearts, six bonnet macaque recipients of transgenic pig skin grafts, and nine rhesus macaque and two capuchin recipients of encapsulated pig islet cells. Serologic screening for PERV antibody was done by a validated Western blot assay, and molecular detection of PERV sequences in peripheral blood mononuclear cells (PBMCs) and plasma was performed using sensitive polymerase chain reaction and reverse transcriptase-polymerase chain reaction assays, respectively. Spleen and lymph node tissues available from six bonnet macaques and three rhesus macaques were also tested for PERV sequences.
RESULTS: All plasma samples were negative for PERV RNA suggesting the absence of viremia in these xenografted animals. Similarly, PERV sequences were not detectable in any PBMC and tissue samples, arguing for the lack of latent infection of these compartments. In addition, all plasma samples were negative for PERV antibodies.
CONCLUSION: These data suggest the absence of PERV infection in all 23 NHPs despite exposure to vascularized porcine organs or tissue xenografts and the use of immunosuppressive therapies in some animals. These findings suggest that PERV is not easily transmitted to these NHP species through these types of xenografts.

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Year:  2001        PMID: 11349732     DOI: 10.1097/00007890-200104150-00022

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  13 in total

1.  Long-term safety from transmission of porcine endogenous retrovirus after pig-to-non-human primate corneal transplantation.

Authors:  Hyuk Jin Choi; Jiyeon Kim; Jae Young Kim; Hyun Ju Lee; Won Ryang Wee; Mee Kum Kim; Eung Soo Hwang
Journal:  Xenotransplantation       Date:  2017-05-14       Impact factor: 3.907

2.  Porcine endogenous retrovirus infects but does not replicate in nonhuman primate primary cells and cell lines.

Authors:  Armin Ritzhaupt; Luc J W Van Der Laan; Daniel R Salomon; Carolyn A Wilson
Journal:  J Virol       Date:  2002-11       Impact factor: 5.103

3.  Monitoring for presence of potentially xenotic viruses in recipients of pig islet xenotransplantation.

Authors:  O Garkavenko; M C Croxson; M Irgang; A Karlas; J Denner; R B Elliott
Journal:  J Clin Microbiol       Date:  2004-11       Impact factor: 5.948

Review 4.  Infection barriers to successful xenotransplantation focusing on porcine endogenous retroviruses.

Authors:  Joachim Denner; Ralf R Tönjes
Journal:  Clin Microbiol Rev       Date:  2012-04       Impact factor: 26.132

5.  Mouse retrovirus mediates porcine endogenous retrovirus transmission into human cells in long-term human-porcine chimeric mice.

Authors:  Yong-Guang Yang; James C Wood; Ping Lan; Robert A Wilkinson; Megan Sykes; Jay A Fishman; Clive Patience
Journal:  J Clin Invest       Date:  2004-09       Impact factor: 14.808

6.  Susceptibility of porcine endogenous retrovirus to anti-retroviral inhibitors.

Authors:  Takele Argaw; Winston Colon-Moran; Carolyn Wilson
Journal:  Xenotransplantation       Date:  2016-03-29       Impact factor: 3.907

7.  Suboptimal porcine endogenous retrovirus infection in non-human primate cells: implication for preclinical xenotransplantation.

Authors:  Giada Mattiuzzo; Yasuhiro Takeuchi
Journal:  PLoS One       Date:  2010-10-06       Impact factor: 3.240

Review 8.  Current progress of genetically engineered pig models for biomedical research.

Authors:  Gökhan Gün; Wilfried A Kues
Journal:  Biores Open Access       Date:  2014-12-01

9.  Novel simian foamy virus infections from multiple monkey species in women from the Democratic Republic of Congo.

Authors:  William M Switzer; Shaohua Tang; Steve Ahuka-Mundeke; Anupama Shankar; Debra L Hanson; HaoQiang Zheng; Ahidjo Ayouba; Nathan D Wolfe; Matthew LeBreton; Cyrille F Djoko; Ubald Tamoufe; Amandine Esteban; Walid Heneine; Martine Peeters; Linda L Wright; Jean Jacques Muyembe-Tamfum; Emile Okitolonda Wemakoy; Prime Mulembakani; Nicole A Hoff; Anne W Rimoin
Journal:  Retrovirology       Date:  2012-12-05       Impact factor: 4.602

Review 10.  Tissue engineering and cell based therapies, from the bench to the clinic: the potential to replace, repair and regenerate.

Authors:  William L Fodor
Journal:  Reprod Biol Endocrinol       Date:  2003-11-13       Impact factor: 5.211

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