Evidence map›Paper›PMID 24909159›Full record

ArticleNature communications2014

Differential developmental requirement and peripheral regulation for dermal Vγ4 and Vγ6T17 cells in health and inflammation.

Yihua Cai, Feng Xue, Chris Fleming, Jie Yang, Chuanlin Ding, Yunfeng Ma, Min Liu, Huang-ge Zhang, Jie Zheng, Na Xiong and 1 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Nature communications, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

93 citing papers in PubMed, 157 citations in OpenAlex.

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  12. ANKRD22 promotes resolution of psoriasiform skin inflammation by antagonizing NIK-mediated IL-23 production.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
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33 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 2 countries.

Yihua Cai1] James Graham Brown Cancer Center, Department of Medicine and Department of Microbiology and Immunology, University of Louisville, Louisville, Kentucky 40202, USA [2].
Feng Xue1] Department of Dermatology, Ruijin Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai 200025, China [2].
Chris FlemingJames Graham Brown Cancer Center, Department of Medicine and Department of Microbiology and Immunology, University of Louisville, Louisville, Kentucky 40202, USA.
Jie YangCenter for Molecular Immunology and Infectious Diseases and Department of Veterinary and Biomedical Sciences, Pennsylvania State University, University Park, Pennsylvania 16802, USA.
Chuanlin DingJames Graham Brown Cancer Center, Department of Medicine and Department of Microbiology and Immunology, University of Louisville, Louisville, Kentucky 40202, USA.
Yunfeng MaJames Graham Brown Cancer Center, Department of Medicine and Department of Microbiology and Immunology, University of Louisville, Louisville, Kentucky 40202, USA.
Min LiuJames Graham Brown Cancer Center, Department of Medicine and Department of Microbiology and Immunology, University of Louisville, Louisville, Kentucky 40202, USA.
Huang-ge ZhangJames Graham Brown Cancer Center, Department of Medicine and Department of Microbiology and Immunology, University of Louisville, Louisville, Kentucky 40202, USA.
Jie ZhengDepartment of Dermatology, Ruijin Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai 200025, China.
Na XiongCenter for Molecular Immunology and Infectious Diseases and Department of Veterinary and Biomedical Sciences, Pennsylvania State University, University Park, Pennsylvania 16802, USA.
Jun YanJames Graham Brown Cancer Center, Department of Medicine and Department of Microbiology and Immunology, University of Louisville, Louisville, Kentucky 40202, USA.
University of Louisville · USPennsylvania State University · USRuijin Hospital · CN

Funding

Mechanisms of Immune Modulation Mediated by Yeast-derived Particulate Beta-GlucanR01CA150947 · NCI · UNIVERSITY OF LOUISVILLE · PI YAN, JUN · 2009 to 2012
$1.5M
NCI NIH HHS R01 CA150947
6 · The paper itself

Abstract

Dermal IL-17-producing γδT cells have a critical role in skin inflammation. However, their development and peripheral regulation have not been fully elucidated. Here we demonstrate that dermal γδT cells develop from the embryonic thymus and undergo homeostatic proliferation after birth with diversified TCR repertoire. Vγ6T cells are bona fide resident, but precursors of dermal Vγ4T cells may require extrathymic environment for imprinting skin-homing properties. Thymic Vγ6T cells are more competitive than Vγ4 for dermal γδT cell reconstitution and TCRδ(-/-) mice reconstituted with Vγ6 develop psoriasis-like inflammation after IMQ-application. Although both IL-23 and IL-1β promote Vγ4 and Vγ6 proliferation, Vγ4 are the main source of IL-17 production that requires IL-1 signalling. Mice with deficiency of IL-1RI signalling have significantly decreased skin inflammation. These studies reveal a differential developmental requirement and peripheral regulation for dermal Vγ6 and Vγ4 γδT cells, implying a new mechanism that may be involved in skin inflammation.

Indexed as

AnimalsCell ProliferationInflammationInterleukin-1Interleukin-17MiceMice, Inbred C57BLMice, KnockoutReceptors, Antigen, T-Cell, gamma-deltaSignal TransductionSkinInterleukin-1Interleukin-17Receptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID24909159
PMCPMC4068267
OpenAlexW2161972318

What OpenQuestion holds

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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.