Evidence map›Paper›PMID 29722117›Full record

ArticleTransplant international : official journal of the European Society for Organ Transplantation2018

Upregulation of CD80 on glomerular podocytes plays an important role in development of proteinuria following pig-to-baboon xeno-renal transplantation - an experimental study.

Christopher J Rivard, Tatsu Tanabe, Miguel A Lanaspa, Hironosuke Watanabe, Shunichiro Nomura, Ana Andres-Hernando, Krystle Garth, Mitsuhiro Sekijima, Takuji Ishimoto, Yuichi Ariyoshi and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Transplant international : official journal of the European Society for Organ Transplantation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

27 citing papers in PubMed, 39 citations in OpenAlex.

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  10. De novo membranous nephropathy in a pig-to-baboon kidney xenograft: A new xenograft glomerulopathy.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2024
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  14. Clinically available immunosuppression averts rejection but not systemic inflammation after porcine islet xenotransplant in cynomolgus macaques.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2022
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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

19 authors at 3 institutions in 1 country.

Christopher J RivardDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, USA.
Tatsu TanabeColumbia Center for Translational Immunology, Columbia University Medical Center, New York, NY, USA.
Miguel A LanaspaDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, USA.
Hironosuke WatanabeColumbia Center for Translational Immunology, Columbia University Medical Center, New York, NY, USA.
Shunichiro NomuraColumbia Center for Translational Immunology, Columbia University Medical Center, New York, NY, USA.
Ana Andres-HernandoDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, USA.
Krystle GarthDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, USA.
Mitsuhiro SekijimaTBRC Laboratories, CTS, Massachusetts General Hospital, Charlestown, MA, USA.
Takuji IshimotoDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, USA.
Yuichi AriyoshiColumbia Center for Translational Immunology, Columbia University Medical Center, New York, NY, USA.
Gabriela E GarciaDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, USA.
Jigesh ShahTBRC Laboratories, CTS, Massachusetts General Hospital, Charlestown, MA, USA.
Boyd LennanColumbia Center for Translational Immunology, Columbia University Medical Center, New York, NY, USA.
Masayuki TasakiTBRC Laboratories, CTS, Massachusetts General Hospital, Charlestown, MA, USA.
Thomas PomposelliColumbia Center for Translational Immunology, Columbia University Medical Center, New York, NY, USA.
Akira ShimizuTBRC Laboratories, CTS, Massachusetts General Hospital, Charlestown, MA, USA.
David H SachsColumbia Center for Translational Immunology, Columbia University Medical Center, New York, NY, USA.
Richard J JohnsonDivision of Renal Diseases and Hypertension, University of Colorado Denver, Aurora, CO, USA.
Kazuhiko YamadaColumbia Center for Translational Immunology, Columbia University Medical Center, New York, NY, USA.ORCID 0000-0002-0510-5843
Columbia University Irving Medical Center · USUniversity of Colorado Denver · USMassachusetts General Hospital · US

Funding

XENOGRAFT TOLERANCE THROUGH MIXED CHIMERISMP01AI045897 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Megan Sykes · 2000 to 2026
$71.9M
PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Wendy M Kohrt · 1995 to 2026
$32.6M
POSTDOCTORAL TRAINING IN CARDIOVASCULAR DISEASET32HL007854 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Marwah Abdalla, Michael Argenziano · 1996 to 2026
$14.7M
Bristol-Myers SquibbNHLBI NIH HHS T32 HL007854NIAID NIH HHS P01 AI045897NIH HHS 2P01AI45897NIH HHS 6PO1AI45897
6 · The paper itself

Abstract

We have previously reported that co-transplantation of the kidney with vascularized donor thymus from α-1,3-galactosyltransferase gene knockout pigs with an anti-CD154 with rituximab-based regimen led to improved xenograft survival in baboons with donor-specific unresponsiveness. However, nephrotic syndrome emerged as a complication in which the glomeruli showed mild mesangial expansion with similarities to minimal change disease (MCD) in humans. Since MCD is associated with CD80 expression in glomeruli and elevated urinary excretion, we evaluated a potential role for CD80 in xenograft nephropathy. Study 1 confirmed high urinary CD80 excretion in nephrotic animals with renal xenografts showing CD80 expression in glomeruli. In Study 2, baboons receiving xenografts received CTLA4-Ig once a week from the second postoperative week or no CTLA4-Ig. The non-CTLA4-Ig group developed severe proteinuria with modest mesangial expansion with high urinary excretion of CD80 and documented CD80 expression in glomerular podocytes. All of the recipients in non-CTLA4-Ig groups had to be euthanized before POD 60. In contrast, CTLA4-Ig group showed a marked reduction in proteinuria and survived significantly longer, up to 193 days. These results demonstrate that anti-CD80 targeted therapy represents a promising strategy for reduction of proteinuria following renal xeno-transplantation with improved survival.

Indexed as

Gene Expression RegulationKidney TransplantationAbataceptAnimalsAnimals, Genetically ModifiedB7-1 AntigenCD40 LigandCTLA-4 AntigenGalactosyltransferasesImmunoglobulin GKidneyKidney DiseasesKidney GlomerulusNephrosisNephrosis, LipoidPapioAbataceptalpha-1,3-galactosyltransferase 1, porcineB7-1 AntigenCD40 LigandCTLA-4 AntigenGalactosyltransferasesImmunoglobulin GCD80kidney transplantationlarge animal modelproteinuriaxenograft

Identifiers

PMID29722117
PMCPMC6407427
OpenAlexW2802104185

What OpenQuestion holds

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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.