Evidence map›Paper›PMID 30760917›Full record

ArticleCellular & molecular immunology2019

The pursuit of transplantation tolerance: new mechanistic insights.

Pawan K Gupta, Christine M McIntosh, Anita S Chong, Maria-Luisa Alegre

Abstract read
In one paragraph

Article in Cellular & molecular immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Reduced Satb1 expression predisposes CD4Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  6. Article
  7. CD3e-immunotoxin spares CD62LFrontiers in immunology · 2022
    Article
  8. Article
  9. Article
  10. Review
  11. 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.

Pawan K GuptaDepartment of Medicine, The University of Chicago, Chicago, IL, 60637, USA.
Christine M McIntoshDepartment of Medicine, The University of Chicago, Chicago, IL, 60637, USA.
Anita S ChongDepartment of Surgery, The University of Chicago, Chicago, IL, 60637, USA.
Maria-Luisa AlegreDepartment of Medicine, The University of Chicago, Chicago, IL, 60637, USA. malegre@midway.uchicago.edu.

Funding

ULTRASTRUCTURE AND CYTOMORPHOLOGY COREP30DK042086 · NIDDK · UNIVERSITY OF CHICAGO · PI CHANG, EUGENE B · 1990 to 2025
$29.8M
T cell mechanisms that distinguish robust tolerance from metastable allograft acceptance and failed tolerance (Project 2)P01AI097113 · NIAID · UNIVERSITY OF CHICAGO · PI Maria-Luisa Alegre, Anita S Chong · 2012 to 2026
$23.8M
Ruth L. Kirschstein National Research Service Award (NRSA) Institutional Research Training Grant (Parent T32)T32HD007009 · NICHD · UNIVERSITY OF CHICAGO · PI NANCY B SCHWARTZ · 1985 to 2026
$13.0M
Deconstructing B cell transplantation toleranceR01AI142747 · NIAID · UNIVERSITY OF CHICAGO · PI CHONG, ANITA S · 2019 to 2022
$2.2M
NIAID NIH HHS P01 AI097113NIAID NIH HHS R01 AI142747NICHD NIH HHS T32 HD007009NIDDK NIH HHS P30 DK042086
6 · The paper itself

Abstract

Donor-specific transplantation tolerance that enables weaning from immunosuppressive drugs but retains immune competence to non-graft antigens has been a lasting pursuit since the discovery of neonatal tolerance. More recently, efforts have been devoted not only to understanding how transplantation tolerance can be induced but also the mechanisms necessary to maintain it as well as how inflammatory exposure challenges its durability. This review focuses on recent advances regarding key peripheral mechanisms of T cell tolerance, with the underlying hypothesis that a combination of several of these mechanisms may afford a more robust and durable tolerance and that a better understanding of these individual pathways may permit longitudinal tracking of tolerance following clinical transplantation to serve as biomarkers. This review may enable a personalized assessment of the degree of tolerance in individual patients and the opportunity to strengthen the robustness of peripheral tolerance.

Indexed as

Transplantation ToleranceAnimalsB-Lymphocytes, RegulatoryGraft RejectionHumansImmunosuppression TherapyIsoantigensT-Lymphocytes, RegulatoryIsoantigensT cell dysfunctionTCR aviditytoleranceTreg

Identifiers

PMID30760917
PMCPMC6461908

What Socratic holds

Textmetadata
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 Socratic graph.