Evidence map›Paper›PMID 30134172›Full record

ArticleCell reports2018

Distinct Graft-Specific TCR Avidity Profiles during Acute Rejection and Tolerance.

Michelle L Miller, Christine M McIntosh, Jason B Williams, Ying Wang, Maile K Hollinger, Noel J Isaad, James J Moon, Thomas F Gajewski, Anita S Chong, Maria-Luisa Alegre

Abstract read
In one paragraph

Article in Cell reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Low-affinity CD8American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2024
    Article
  2. Article
  3. Article
  4. Oral alloantigen exposure promotes donor-specific tolerance in a mouse model of minor-mismatched skin transplantation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2022
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Resilience of T cell-intrinsic dysfunction in transplantation tolerance.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  13. Outstanding questions in transplantation: B cells, alloantibodies, and humoral rejection.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2019
    Review
  14. Article
  15. Article
  16. Tolerating Factor VIII: Recent Progress.Frontiers in immunology · 2019
    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

10 authors.

Michelle L MillerDepartment of Medicine, Section of Rheumatology, The University of Chicago, Chicago, IL 60637, USA.
Christine M McIntoshDepartment of Medicine, Section of Rheumatology, The University of Chicago, Chicago, IL 60637, USA.
Jason B WilliamsDepartment of Pathology, The University of Chicago, Chicago, IL 60637, USA.
Ying WangDepartment of Medicine, Section of Rheumatology, The University of Chicago, Chicago, IL 60637, USA.
Maile K HollingerDepartment of Medicine, Section of Rheumatology, The University of Chicago, Chicago, IL 60637, USA.
Noel J IsaadDepartment of Medicine, Section of Rheumatology, The University of Chicago, Chicago, IL 60637, USA.
James J MoonCenter for Immunology and Inflammatory Diseases and Division of Pulmonary and Critical Care Medicine, Massachusetts General Hospital, Charlestown, MA 02129, USA; Harvard Medical School, Charlestown, MA 02129, USA.
Thomas F GajewskiDepartment of Pathology, The University of Chicago, Chicago, IL 60637, USA.
Anita S ChongDepartment of Surgery, Section of Transplantation, The University of Chicago, Chicago, IL 60637, USA.
Maria-Luisa AlegreDepartment of Medicine, Section of Rheumatology, The University of Chicago, Chicago, IL 60637, USA. Electronic address: malegre@midway.uchicago.edu.

Funding

Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG · 1991 to 2026
$35.3M
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
INTERDISCIPLINARY TRAINING PROGRAM IN IMMUNOLOGYT32AI007090 · NIAID · UNIVERSITY OF CHICAGO · PI Peter Aidan Savage · 1985 to 2026
$11.7M
University of Chicago Initiative for Maximizing Student Development (IMSD) - Renewal 01R25GM109439 · NIGMS · UNIVERSITY OF CHICAGO · PI SCHWARTZ, NANCY B · 2014 to 2023
$5.7M
CARDIOVASCULAR PATHOPHYSIOLOGY &BIOCHEMISTRY TRAININGT32HL007237 · NHLBI · UNIVERSITY OF CHICAGO · PI GETZ, GODFREY SHALOM · 1985 to 2011
$5.0M
Self Antigen Specific CD4 Positive T cellsR01AI107020 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI MOON, JAMES J · 2014 to 2018
$2.1M
American Heart Association-American Stroke Association 13PRE14550022NHLBI NIH HHS T32 HL007237NIAID NIH HHS P01 AI097113NIAID NIH HHS R01 AI107020NIAID NIH HHS T32 AI007090NICHD NIH HHS T32 HD007009NIDDK NIH HHS P30 DK043351NIGMS NIH HHS R25 GM109439
6 · The paper itself

Abstract

Mechanisms implicated in robust transplantation tolerance at the cellular level can be broadly categorized into those that inhibit alloreactive T cells intrinsically (clonal deletion and dysfunction) or extrinsically through regulation. Here, we investigated whether additional population-level mechanisms control T cells by examining whether therapeutically induced peripheral transplantation tolerance could influence T cell populations' avidity for alloantigens. Whereas T cells with high avidity preferentially accumulated during acute rejection of allografts, the alloreactive T cells in tolerant recipients retained a low-avidity profile, comparable to naive mice despite evidence of activation. These contrasting avidity profiles upon productive versus tolerogenic stimulation were durable and persisted upon alloantigen re-encounter in the absence of any immunosuppression. Thus, peripheral transplantation tolerance involves control of alloreactive T cells at the population level, in addition to the individual cell level. Controlling expansion or eliminating high-affinity, donor-specific T cells long term may be desirable to achieve robust transplantation tolerance in the clinic.

Indexed as

AnimalsGraft RejectionHumansImmune ToleranceMiceTransplantation ToleranceaffinityaviditycostimulationmousepMHC multimerT cellsTCRtolerancetransplantation

Identifiers

PMID30134172
PMCPMC6142813

What Socratic 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 Socratic graph.