Evidence map›Paper›PMID 33533717›Full record

ArticleeLife2021

Gut Helicobacter presentation by multiple dendritic cell subsets enables context-specific regulatory T cell generation.

Emilie V Russler-Germain, Jaeu Yi, Shannon Young, Katherine Nutsch, Harikesh S Wong, Teresa L Ai, Jiani N Chai, Vivek Durai, Daniel H Kaplan, Ronald N Germain and 2 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

27 citing papers in PubMed, 35 citations in OpenAlex.

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  17. The emerging family of RORγtNature reviews. Immunology · 2024
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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 3 institutions in 1 country.

Emilie V Russler-GermainDepartment of Internal Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, United States.ORCID 0000-0002-2036-6697
Jaeu YiDepartment of Internal Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, United States.
Shannon YoungDepartment of Internal Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, United States.
Katherine NutschDepartment of Internal Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, United States.
Harikesh S WongLymphocyte Biology Section, Laboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, United States.
Teresa L AiDepartment of Internal Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, United States.
Jiani N ChaiDepartment of Internal Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, United States.ORCID 0000-0003-2560-8218
Vivek DuraiDepartment of Pathology, Division of Immunobiology, Washington University School of Medicine, St. Louis, United States.
Daniel H KaplanDepartment of Dermatology, Department of Immunology, Pittsburgh Center for Pain Research, University of Pittsburgh, Pittsburgh, United States.
Ronald N GermainLymphocyte Biology Section, Laboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, United States.ORCID 0000-0003-1495-9143
Kenneth M MurphyDepartment of Pathology, Division of Immunobiology, Washington University School of Medicine, St. Louis, United States.
Chyi-Song HsiehDepartment of Internal Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, United States.
Washington University in St. Louis · USNational Institutes of Health · USUniversity of Pittsburgh · US

Funding

NATIONAL RESEARCH SERVICE AWARD-MEDICAL SCIENTISTT32GM007200 · NIGMS · WASHINGTON UNIVERSITY · PI YOKOYAMA, WAYNE M. · 1985 to 2024
$59.8M
Functional Biology Of T CellsZIAAI000758 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI GERMAIN, RONALD N · 2009 to 2025
$15.4M
UNIQUE ROLES OF ANTIGEN PRESENTING CELLS ON T CELL TOLERANCE AND AUTOIMMUNITYR01AI079187 · NIAID · WASHINGTON UNIVERSITY · PI HSIEH, CHYI S · 2008 to 2021
$5.8M
The Role of Route of Entry by Bacterial Antigens on Colonic T Cell ResponsesR01AI136515 · NIAID · WASHINGTON UNIVERSITY · PI HSIEH, CHYI S, NEWBERRY, RODNEY D · 2018 to 2022
$2.8M
The Role of CD101 in T Cell Tolerance in the GutF30DK111071 · NIDDK · WASHINGTON UNIVERSITY · PI RUSSLER-GERMAIN, EMILIE VERONICA · 2016 to 2018
$110k
NIAID NIH HHS R01 AI079187NIAID NIH HHS R01 AI136515NIDDK NIH HHS F30 DK111071NIH HHS F30 DK111071NIH HHS T32 GM007200
6 · The paper itself

Abstract

Generation of tolerogenic peripheral regulatory T (pTreg) cells is commonly thought to involve CD103

Indexed as

AnimalsCell DifferentiationCell MovementColonDendritic CellsHelicobacterLymph NodesMiceMice, KnockoutMice, TransgenicT-Lymphocytes, Regulatorycolondendritic cellHelicobacterimmunologyinflammationmicrobiotamouseregulatory t celltolerance

Identifiers

PMID33533717
PMCPMC7877908
OpenAlexW3128553104

What OpenQuestion holds

Textmetadata
LicenceCC0
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.