Evidence map›Paper›PMID 29624743›Full record

ArticleXenotransplantation2018

Absence of interaction between porcine endogenous retrovirus and porcine cytomegalovirus in pig-to-baboon renal xenotransplantation in vivo.

Jay A Fishman, David H Sachs, Kazuhiko Yamada, Robert A Wilkinson

Abstract read
In one paragraph

Article in Xenotransplantation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Infection in xenotransplantation: opportunities and challenges.Current opinion in organ transplantation · 2019
    Review
  7. Review
  8. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Jay A FishmanInfectious Disease Division and MGH Transplant Center, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.ORCID 0000-0002-2671-3311
David H SachsColumbia Center for Translational Immunology, Departments of Medicine and Surgery, Columbia University, New York, NY, USA.
Kazuhiko YamadaColumbia Center for Translational Immunology, Departments of Medicine and Surgery, Columbia University, New York, NY, USA.ORCID 0000-0002-0510-5843
Robert A WilkinsonInfectious Disease Division and MGH Transplant Center, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Columbia University Irving Medical Center · USHarvard University · US

Funding

XENOGRAFT TOLERANCE THROUGH MIXED CHIMERISMP01AI045897 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Megan Sykes · 2000 to 2026
$71.9M
TOLERANCE TO VASCULARIZED ALLOGRAFTS IN MINISWINER01AI031046 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI SACHS, DAVID H · 1991 to 2005
$3.3M
RES FACIL CONST: XENOTRANSPLANTATION, LUNG ALLOGRAFT REJECTION IN SWINEC06RR020135 · NCRR · MASSACHUSETTS GENERAL HOSPITAL · PI SLAVIN, PETER L · 2004 to 2004
$2.7M
MGH Swine Facility Grant C06 RR020135-01National Institute of Allergy and Infectious Diseases 2P01AI45897NCRR NIH HHS C06 RR020135NIAID NIH HHS P01 AI045897NIAID NIH HHS R01 AI031046
6 · The paper itself

Abstract

backgroundStudies of xenotransplantation from swine have identified porcine viruses as potential barriers to clinical trials. The biology of these viruses has not been extensively investigated in the in vivo xeno-environment. Enhancement of viral gene expression by viral and cellular factors acting in trans has been demonstrated for certain viruses, including bidirectional interactions between human herpesviruses and endogenous (HERV) and exogenous (HIV) retroviruses. Both porcine cytomegalovirus (PCMV) and porcine endogenous retrovirus (PERV) infections have been identified in xenografts from swine. PERV receptors exist on human cells with productive infection in vitro in permissive human target cell lines. PCMV is largely species-specific with infection restricted to the xenograft in pig-to-baboon transplants. It is unknown whether coinfection by PCMV affects the replication of PERV within xenograft tissues which might have implications for the risk of retroviral infection in the human host.

methodsA series of 11 functioning, life-supporting pig-to-baboon kidney xenografts from PERV-positive miniature swine were studied with and without PCMV co-infection. Frozen biopsy samples were analyzed using quantitative, real-time PCR with internal controls.

resultsPERV replication was not altered in the presence of PCMV coinfection (P = .70). The absence of variation with coinfection was confirmed when PERV quantitation was expressed relative to simultaneous cellular GAPDH levels with or without PCMV coinfection (P = .59).

conclusionsPCMV coinfection does not alter the replication of PERV in life-supporting renal xenotransplantation in vivo in baboons.

Indexed as

Transplantation, HeterologousAnimalsCytomegalovirusDNA, ViralEndogenous RetrovirusesHeterograftsHumansKidneyPapioPapio hamadryasRetroviridae InfectionsSwineDNA, Viralinfectionporcine cytomegalovirusporcine endogenous retrovirussafetyxenotransplantation

Identifiers

PMID29624743
PMCPMC6158079
OpenAlexW2795773064

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.