Evidence map›Paper›PMID 31182480›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2019

Early Notch Signals Induce a Pathogenic Molecular Signature during Priming of Alloantigen-Specific Conventional CD4

Jooho Chung, Vedran Radojcic, Eric Perkey, Timothy J Parnell, Yashar Niknafs, Xi Jin, Ann Friedman, Nathalie Labrecque, Bruce R Blazar, Todd V Brennan and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 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
1.1field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Dll1Nature communications · 2021
    Article
  9. Review
  10. GCNT1-MediatedJournal of immunology (Baltimore, Md. : 1950) · 2020
    Article
  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

12 authors at 5 institutions in 2 countries.

Jooho ChungGraduate Program in Cellular and Molecular Biology, University of Michigan, Ann Arbor, MI 48109.
Vedran RadojcicDivision of Hematology-Oncology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109.ORCID 0000-0002-9699-1157
Eric PerkeyGraduate Program in Cellular and Molecular Biology, University of Michigan, Ann Arbor, MI 48109.
Timothy J ParnellHuntsman Cancer Institute Bioinformatic Analysis Shared Resource, University of Utah, Salt Lake City, UT 84112.ORCID 0000-0002-3632-3691
Yashar NiknafsGraduate Program in Cellular and Molecular Biology, University of Michigan, Ann Arbor, MI 48109.
Xi JinDivision of Hematology-Oncology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109.
Ann FriedmanLife Sciences Institute, University of Michigan, Ann Arbor, MI 48109.
Nathalie LabrecqueCentre de Recherche Hôpital Maisonneuve-Rosemont, Université de Montréal, Montreal, Quebec H1T 2M4, Canada.ORCID 0000-0001-7563-1542
Bruce R BlazarDivision of Blood and Marrow Transplantation, Department of Pediatrics, University of Minnesota, Minneapolis, MN 55455.ORCID 0000-0002-9608-9841
Todd V BrennanComprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, CA 90048.ORCID 0000-0001-5940-5262
Christian W SiebelGenentech, South San Francisco, CA 94080; and.
Ivan MaillardLife Sciences Institute, University of Michigan, Ann Arbor, MI 48109; imaillar@pennmedicine.upenn.edu.ORCID 0000-0003-1312-6748
University of Michigan · USUniversity of Utah · USCedars-Sinai Medical Center · USHôpital Maisonneuve-Rosemont · CAUniversity of Minnesota · US

Funding

MICHIGAN MEDICAL SCIENTIST TRAINING PROGRAMT32GM007863 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI COLLINS, KATHLEEN L. · 1985 to 2024
$38.3M
Project 3: Humoral Targets and B Cell Biology in Chronic Graft-vs.-Host DiseaseP01CA142106 · NCI · DANA-FARBER CANCER INST · PI CUTLER, COREY S · 2009 to 2019
$17.5M
CELLULAR AND MOLECULAR BIOLOGY AT MICHIGANT32GM007315 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PUTHENVEEDU, MANOJKUMAR A · 1985 to 2021
$12.8M
Enhancing Treg Therapeutic Efficacy in GVHDR01HL118979 · NHLBI · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R, HIPPEN, KELI L · 2014 to 2025
$6.7M
Notch Signaling in AlloimmunityR01AI091627 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI PEAR, WARREN S · 2011 to 2025
$6.0M
T-CELL TARGETING FOR GVHDR01HL056067 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R · 1995 to 2022
$5.4M
In Vivo Prevention of Murine GVHDR37AI034495 · NIAID · UNIVERSITY OF MINNESOTA · PI Bruce R Blazar · 2017 to 2026
$5.4M
T CELL TARGETING FOR GVHDR37HL056067 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R. · 1998 to 2007
$3.2M
The role of secondary lymphoid organ fibroblastic cells in alloimmunityF30AI136315 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PERKEY, ERIC THOMAS · 2018 to 2021
$166k
NCI NIH HHS P01 CA142106NHLBI NIH HHS R01 HL056067NHLBI NIH HHS R01 HL118979NHLBI NIH HHS R37 HL056067NIAID NIH HHS F30 AI136315NIAID NIH HHS R01 AI091627NIAID NIH HHS R37 AI034495NIGMS NIH HHS T32 GM007315NIGMS NIH HHS T32 GM007863
6 · The paper itself

Abstract

Graft-versus-host disease (GVHD) is the most serious complication of allogeneic hematopoietic cell transplantation. Notch signals delivered during the first 48 h after transplantation drive proinflammatory cytokine production in conventional T cells (Tconv) and inhibit the expansion of regulatory T cells (Tregs). Short-term Notch inhibition induces long-term GVHD protection. However, it remains unknown whether Notch blockade blunts GVHD through its effects on Tconv, Tregs, or both and what early Notch-regulated molecular events occur in alloantigen-specific T cells. To address these questions, we engineered T cell grafts to achieve selective Notch blockade in Tconv versus Tregs and evaluated their capacity to trigger GVHD in mice. Notch blockade in Tconv was essential for GVHD protection as GVHD severity was similar in the recipients of wild-type Tconv combined with Notch-deprived versus wild-type Tregs. To identify the impact of Notch signaling on the earliest steps of T cell activation in vivo, we established a new acute GVHD model mediated by clonal alloantigen-specific 4C CD4

Indexed as

AnimalsBone Marrow TransplantationCD4-Positive T-LymphocytesGraft vs Host DiseaseHematopoietic Stem Cell TransplantationIsoantigensLymphocyte ActivationMiceMice, Inbred BALB CMice, Inbred C57BLMice, TransgenicReceptors, NotchSignal TransductionT-Lymphocytes, RegulatoryTransplantation, HomologousIsoantigensReceptors, Notch

Identifiers

PMID31182480
PMCPMC6615974
OpenAlexW2950920543

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.