Evidence map›Paper›PMID 36322627›Full record

Trial reportScience translational medicine2022

Selective decrease of donor-reactive T

Qizhi Tang, Joey Leung, Yani Peng, Alberto Sanchez-Fueyo, Juan-Jose Lozano, Alice Lam, Karim Lee, John R Greenland, Marc Hellerstein, Mark Fitch and 12 more

Open access · greenAbstract readClinical Trial, Phase IIClinical Trial, Phase I
In one paragraph

Trial report in Science translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

57 citing papers in PubMed, 67 citations in OpenAlex.

  1. Trial
  2. Pharmacokinetics, lineage identity, and trafficking of ex vivo expanded polyclonal regulatory T cells in a prospective randomized clinical trial of kidney transplant recipients with allograft inflammation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2026
    Trial
  3. Selective impact on regulatory T cells with sustained functional phenotypes by the interleukin-2 mutein VIS171 in a nonhuman primate model.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2026
    Article
  4. Article
  5. Decoding TNF receptor superfamily control of CD4Cell communication and signaling : CCS · 2026
    Review
  6. Review
  7. Article
  8. The Role of CD4Cells · 2026
    Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Lactic acid improves Treg manufacturing andMolecular therapy. Methods & clinical development · 2025
    Article
  15. Why regulatory T cells love lactic acid.Molecular therapy. Methods & clinical development · 2025
    Article
  16. Review
  17. Article
  18. Article
  19. HLA-A2 CAR/IL-2-CISC engineered Treg display robustMolecular therapy. Methods & clinical development · 2025
    Article
  20. 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

22 authors at 9 institutions in 3 countries.

Qizhi TangDepartment of Surgery, University of California, San Francisco, San Francisco, CA 94143, USA.ORCID 0000-0001-7313-3574
Joey LeungDepartment of Surgery, University of California, San Francisco, San Francisco, CA 94143, USA.ORCID 0000-0002-2528-9555
Yani PengDepartment of Surgery, University of California, San Francisco, San Francisco, CA 94143, USA.ORCID 0000-0002-3711-7160
Alberto Sanchez-FueyoInstitute of Liver Studies, School of Immunology and Microbial Sciences, King's College London University, London WC2R 2LS, UK.
Juan-Jose LozanoBioinformatic Platform, Biomedical Research Center in Hepatic and Digestive Diseases, Instituto de Salud Carlos III, 28029 Madrid, Spain.
Alice LamDepartment of Surgery, University of California, San Francisco, San Francisco, CA 94143, USA.
Karim LeeDepartment of Surgery, University of California, San Francisco, San Francisco, CA 94143, USA.
John R GreenlandDepartment of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA.ORCID 0000-0003-1422-8367
Marc HellersteinNutrition Sciences and Toxicology, University of California, Berkeley, Berkeley, CA 94720, USA.ORCID 0000-0002-2327-0834
Mark FitchNutrition Sciences and Toxicology, University of California, Berkeley, Berkeley, CA 94720, USA.ORCID 0000-0001-9058-4529
Kelvin W LiNutrition Sciences and Toxicology, University of California, Berkeley, Berkeley, CA 94720, USA.ORCID 0000-0002-1771-1998
Jonathan H EsenstenGladstone-UCSF Institute of Genomic Immunology, San Francisco, CA 94158, USA.
Amy L PutnamDiabetes Center, University of California, San Francisco, San Francisco, CA 94143, USA.
Angela LaresDiabetes Center, University of California, San Francisco, San Francisco, CA 94143, USA.ORCID 0000-0001-8796-4627
Vinh NguyenDepartment of Surgery, University of California, San Francisco, San Francisco, CA 94143, USA.
Weihong LiuDiabetes Center, University of California, San Francisco, San Francisco, CA 94143, USA.
Nancy D BridgesNational Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20852, USA.ORCID 0000-0002-1140-5201
Jonah OdimNational Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20852, USA.ORCID 0000-0003-3465-8647
Anthony J DemetrisThomas E. Starzl Transplantation Institute and Department of Pathology, University of Pittsburgh, Pittsburgh, PA 15213, USA.ORCID 0000-0002-9582-3733
Josh LevitskyDepartment of Medicine, Northwestern University, Chicago, IL 60611, USA.ORCID 0000-0001-7527-6093
Timucin TanerDepartments of Surgery and Immunology, Mayo Clinic, Rochester, MN 55905, USA.
Sandy FengDepartment of Surgery, University of California, San Francisco, San Francisco, CA 94143, USA.ORCID 0000-0002-2601-4350
University of California, San Francisco · USUniversity of California, Berkeley · USGladstone Institutes · USNational Institute of Allergy and Infectious Diseases · USInstituto de Salud Carlos III · ESKing's College London · GBMayo Clinic · USNorthwestern University · USUniversity of Pittsburgh · US

Funding

Research BaseP30DK063720 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VAISSE, CHRISTIAN · 2003 to 2019
$21.8M
Polyclonal Tregs to Promote Tolerance in Pediatric Liver Transplant RecipientsU01AI104347 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FENG, SANDY · 2013 to 2017
$4.8M
NIAID NIH HHS U01 AI104347NIDDK NIH HHS P30 DK063720
6 · The paper itself

Abstract

Promoting immune tolerance to transplanted organs can minimize the amount of immunosuppressive drugs that patients need to take, reducing lifetime risks of mortality and morbidity. Regulatory T cells (T

Indexed as

Liver TransplantationTransplantation ToleranceGraft RejectionHumansLiving DonorsT-Lymphocytes, Regulatory

Identifiers

PMID36322627
PMCPMC11016119
OpenAlexW4307930376

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.