Evidence map›Paper›PMID 35881490›Full record

ArticleJCI insight2022

Treg suppression of immunity within inflamed allogeneic grafts.

Hehua Dai, Andressa Pena, Lynne Bauer, Amanda Williams, Simon C Watkins, Geoffrey Camirand

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Immunomodulation by allograft endothelial cells.Frontiers in transplantation · 2025
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Delayed graft rejection in autoimmune islet transplantation via biomaterial immunotherapy.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2023
    Article
  12. Article
  13. Review
  14. 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

6 authors at 1 institution in 1 country.

Hehua DaiThomas E. Starzl Transplantation Institute, Departments of Surgery and Immunology, and.
Andressa PenaThomas E. Starzl Transplantation Institute, Departments of Surgery and Immunology, and.
Lynne BauerThomas E. Starzl Transplantation Institute, Departments of Surgery and Immunology, and.
Amanda WilliamsThomas E. Starzl Transplantation Institute, Departments of Surgery and Immunology, and.
Simon C WatkinsCenter for Biologic Imaging, Department of Cell Biology and Physiology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Geoffrey CamirandThomas E. Starzl Transplantation Institute, Departments of Surgery and Immunology, and.
University of Pittsburgh · US

Funding

Mechanisms and promotion of immune regulation by CD4+ regulatory T cells within allograftsU01AI132758 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CAMIRAND, GEOFFREY · 2017 to 2021
$1.9M
NIAID NIH HHS U01 AI132758
6 · The paper itself

Abstract

CD4+Foxp3+ regulatory T cells (Tregs) restrain inflammation and immunity. However, the mechanisms underlying Treg suppressor function in inflamed nonlymphoid tissues remain largely unexplored. Here, we restricted immune responses to nonlymphoid tissues and used intravital microscopy to visualize Treg suppression of rejection by effector T cells (Teffs) within inflamed allogeneic islet transplants. Despite their elevated motility, Tregs preferentially contacted antigen-presenting cells (APCs) over Teffs. Interestingly, Tregs specifically targeted APCs that were extensively and simultaneously contacted by Teffs. In turn, Tregs decreased MHC-II expression on APCs and hindered Teff function. Last, we demonstrate that Treg suppressive function within inflamed allografts required ectonucleotidase CD73 activity, which generated the antiinflammatory adenosine. Consequently, CD73-/- Tregs exhibited fewer contacts with APCs within inflamed allografts compared with WT Tregs, but not in spleen. Overall, our findings demonstrate that Tregs suppress immunity within inflamed grafts through CD73 activity and suggest that Treg-APC direct contacts are central to this process.

Indexed as

Antigen-Presenting CellsT-Lymphocytes, RegulatoryAllograftsAdaptive immunityImmunologyTh1 responseToleranceTransplantation

Identifiers

PMID35881490
PMCPMC9462475
OpenAlexW4288041278

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.