Evidence map›Paper›PMID 28011639›Full record

ArticleThe Journal of biological chemistry2017

Loss of Functionally Redundant p38 Isoforms in T Cells Enhances Regulatory T Cell Induction.

Morisada Hayakawa, Hiroko Hayakawa, Tsvetana Petrova, Patcharee Ritprajak, Ruhcha V Sutavani, Guillermina Yanek Jiménez-Andrade, Yasuyo Sano, Min-Kyung Choo, John Seavitt, Ram K C Venigalla and 4 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

20 citing papers in PubMed, 36 citations in OpenAlex.

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  18. Pleiotropic Effects of IL-33 on CD4Frontiers in immunology · 2019
    Review
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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

14 authors at 6 institutions in 4 countries.

Morisada HayakawaFrom the Cutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, Charlestown, Massachusetts 02129; the Department of Biochemistry, Jichi Medical University, Shimotsuke, Tochigi 329-0498, Japan.
Hiroko HayakawaFrom the Cutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, Charlestown, Massachusetts 02129; the Department of Biochemistry, Jichi Medical University, Shimotsuke, Tochigi 329-0498, Japan.
Tsvetana Petrovathe Division of Cell Signalling and Immunology, School of Life Sciences, Wellcome Trust Building, Dundee DD1 5EH, United Kingdom.
Patcharee RitprajakFrom the Cutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, Charlestown, Massachusetts 02129; the Department of Microbiology and Immunology and Research Unit of Oral Microbiology, Faculty of Dentistry, Chulalongkorn University, Bangkok 10330, Thailand.
Ruhcha V Sutavanithe Division of Cell Signalling and Immunology, School of Life Sciences, Wellcome Trust Building, Dundee DD1 5EH, United Kingdom.
Guillermina Yanek Jiménez-AndradeFrom the Cutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, Charlestown, Massachusetts 02129.
Yasuyo SanoFrom the Cutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, Charlestown, Massachusetts 02129.
Min-Kyung ChooFrom the Cutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, Charlestown, Massachusetts 02129.
John SeavittFrom the Cutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, Charlestown, Massachusetts 02129.
Ram K C VenigallaMRC Protein Phosphorylation Unit, School of Life Sciences, Sir James Black Centre, University of Dundee, Dundee DD1 5EH, United Kingdom.
Kinya Otsuthe Cardiovascular Division, King's College London, London SE5 9NU, United Kingdom.
Katia GeorgopoulosFrom the Cutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, Charlestown, Massachusetts 02129.
J Simon C Arthurthe Division of Cell Signalling and Immunology, School of Life Sciences, Wellcome Trust Building, Dundee DD1 5EH, United Kingdom.
Jin Mo ParkFrom the Cutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, Charlestown, Massachusetts 02129. Electronic address: jmpark@cbrc2.mgh.harvard.edu.
Massachusetts General Hospital · USWellcome Trust · GBChulalongkorn University · THHarvard University · USKing's College London · GBMRC Protein Phosphorylation and Ubiquitylation Unit · GB

Funding

Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Ramnik J Xavier · 1991 to 2026
$35.3M
DERMATOLOGY TRAINING GRANTT32AR007098 · NIAMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI THOMAS S. KUPPER · 1986 to 2026
$8.1M
Regulatory targets of p38 MAP kinase in inflammationR01AI074957 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI PARK, JIN MO · 2009 to 2013
$1.9M
Medical Research CouncilNIAID NIH HHS R01 AI074957NIAMS NIH HHS T32 AR007098NIDDK NIH HHS P30 DK043351
6 · The paper itself

Abstract

The evolutionarily conserved protein kinase p38 mediates innate resistance to environmental stress and microbial infection. Four p38 isoforms exist in mammals and may have been co-opted for new roles in adaptive immunity. Murine T cells deficient in p38α, the ubiquitously expressed p38 isoform, showed no readily apparent cell-autonomous defects while expressing elevated amounts of another isoform, p38β. Mice with T cells simultaneously lacking p38α and p38β displayed lymphoid atrophy and elevated Foxp3

Indexed as

AnimalsForkhead Transcription FactorsMAP Kinase Signaling SystemMiceMice, KnockoutMitogen-Activated Protein Kinase 11Mitogen-Activated Protein Kinase 14Receptors, Antigen, T-CellT-Lymphocytes, RegulatoryTOR Serine-Threonine KinasesForkhead Transcription FactorsFoxp3 protein, mouseMitogen-Activated Protein Kinase 11Mitogen-Activated Protein Kinase 14mTOR protein, mouseReceptors, Antigen, T-CellTOR Serine-Threonine Kinasesimmunologymousep38signal transductionT-cell

Identifiers

PMID28011639
PMCPMC5290950
OpenAlexW2566919111

What Socratic 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 Socratic graph.