Evidence map›Paper›PMID 34752418›Full record

ArticleJCI insight2021

Overexpression of PD-1 on T cells promotes tolerance in cardiac transplantation via ICOS-dependent mechanisms.

Thiago J Borges, Naoka Murakami, Isadora T Lape, Rodrigo B Gassen, Kaifeng Liu, Songjie Cai, Joe Daccache, Kassem Safa, Tetsunosuke Shimizu, Shunsuke Ohori and 7 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.6field-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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Programmed death-ligand 1 on ex vivo-expanded toll-like-receptor-Bregs prevents allograft rejection by Breg viability promotion, CD4American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2026
    Article
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  8. Article
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  12. Immune Checkpoint Inhibitor Therapy for Kidney Transplant Recipients - A Review of Potential Complications and Management Strategies.Transplant international : official journal of the European Society for Organ Transplantation · 2024
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Myocardial-Treg Crosstalk: How to Tame a Wolf.Frontiers in immunology · 2022
    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

17 authors at 4 institutions in 1 country.

Thiago J BorgesCenter for Transplantation Sciences, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Naoka MurakamiTransplantation Research Center, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Isadora T LapeCenter for Transplantation Sciences, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Rodrigo B GassenCenter for Transplantation Sciences, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Kaifeng LiuCenter for Transplantation Sciences, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Songjie CaiTransplantation Research Center, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Joe DaccacheTransplantation Research Center, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Kassem SafaDivision of Nephrology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Tetsunosuke ShimizuTransplantation Research Center, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Shunsuke OhoriTransplantation Research Center, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Alison M PatersonDepartment of Immunology, Blavatnik Institute, Harvard Medical School, Boston, Massachusetts, USA.
Paolo CravediRenal Division, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Jamil AzziTransplantation Research Center, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Peter T SageTransplantation Research Center, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Arlene H SharpeDepartment of Immunology, Blavatnik Institute, Harvard Medical School, Boston, Massachusetts, USA.
Xian C LiImmunobiology and Transplant Science Center, Houston Methodist Hospital, Houston, Texas, USA.
Leonardo V RiellaCenter for Transplantation Sciences, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Brigham and Women's Hospital · USHarvard University · USIcahn School of Medicine at Mount Sinai · USMethodist Hospital · US

Funding

Transgenic/KnockoutP01AI056299 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI SHARPE, ARLENE H. · 2003 to 2023
$42.5M
TRAINING PROGRAM IN ACADEMIC NEPHROLOGYT32DK007527 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI BONVENTRE, JOSEPH VINCENT · 1986 to 2021
$8.8M
Role of Siglec-E in Regulating AlloimmunityR01AI143887 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI RIELLA, LEONARDO V. · 2019 to 2023
$2.1M
Protection of kidney from autoimmunity by modulating co-stimlatory signalingK08DK120868 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI MURAKAMI, NAOKA · 2019 to 2023
$886k
NIAID NIH HHS P01 AI056299NIAID NIH HHS R01 AI143887NIDDK NIH HHS K08 DK120868NIDDK NIH HHS T32 DK007527
6 · The paper itself

Abstract

The programmed death 1/programmed death ligand 1 (PD-1/PD-L1) pathway is a potent inhibitory pathway involved in immune regulation and is a potential therapeutic target in transplantation. In this study, we show that overexpression of PD-1 on T cells (PD-1 Tg) promotes allograft tolerance in a fully MHC-mismatched cardiac transplant model when combined with costimulation blockade with CTLA-4-Ig. PD-1 overexpression on T cells also protected against chronic rejection in a single MHC II-mismatched cardiac transplant model, whereas the overexpression still allowed the generation of an effective immune response against an influenza A virus. Notably, Tregs from PD-1 Tg mice were required for tolerance induction and presented greater ICOS expression than those from WT mice. The survival benefit of PD-1 Tg recipients required ICOS signaling and donor PD-L1 expression. These results indicate that modulation of PD-1 expression, in combination with a costimulation blockade, is a promising therapeutic target to promote transplant tolerance.

Indexed as

AnimalsDisease Models, AnimalHeart TransplantationHumansInducible T-Cell Co-Stimulator ProteinMiceProgrammed Cell Death 1 ReceptorSurvival AnalysisT-LymphocytesInducible T-Cell Co-Stimulator ProteinPDCD1 protein, humanProgrammed Cell Death 1 ReceptorCostimulationImmunologyT cellsToleranceTransplantation

Identifiers

PMID34752418
PMCPMC8783692
OpenAlexW3213481785

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.