Evidence map›Paper›PMID 25367574›Full record

ArticleImmunity2014

miR-155 promotes T follicular helper cell accumulation during chronic, low-grade inflammation.

Ruozhen Hu, Dominique A Kagele, Thomas B Huffaker, Marah C Runtsch, Margaret Alexander, Jin Liu, Erin Bake, Wei Su, Matthew A Williams, Dinesh S Rao and 4 more

Open access · greenAbstract read
In one paragraph

Article in Immunity, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 109 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
109citing papers in PubMed, 1 pooled it
6.5field-weighted citation impact, top 2% 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

109 citing papers in PubMed, 1 synthesis or guideline pooled it, 155 citations in OpenAlex.

  1. Role of miR-155 in inflammatory autoimmune diseases: a comprehensive review.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2022
    Pooled it
  2. Review
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  11. Article
  12. Research Progress on Frailty in Elderly People.Clinical interventions in aging · 2024
    Review
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  15. Review
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  17. Article
  18. Article
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49 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 1 country.

Ruozhen HuDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, 4280 JMRB, 15 North Medical Dr. East, Salt Lake City, UT 84112, USA.
Dominique A KageleDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, 4280 JMRB, 15 North Medical Dr. East, Salt Lake City, UT 84112, USA.
Thomas B HuffakerDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, 4280 JMRB, 15 North Medical Dr. East, Salt Lake City, UT 84112, USA.
Marah C RuntschDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, 4280 JMRB, 15 North Medical Dr. East, Salt Lake City, UT 84112, USA.
Margaret AlexanderDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, 4280 JMRB, 15 North Medical Dr. East, Salt Lake City, UT 84112, USA.
Jin LiuDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, 4280 JMRB, 15 North Medical Dr. East, Salt Lake City, UT 84112, USA.
Erin BakeDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, 4280 JMRB, 15 North Medical Dr. East, Salt Lake City, UT 84112, USA.
Wei SuDepartment of Neurology, University of Washington, Seattle, WA 98195, USA.
Matthew A WilliamsDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, 4280 JMRB, 15 North Medical Dr. East, Salt Lake City, UT 84112, USA.
Dinesh S RaoDepartment of Pathology and Laboratory Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Thomas MöllerDepartment of Neurology, University of Washington, Seattle, WA 98195, USA.
Gwenn A GardenDepartment of Neurology, University of Washington, Seattle, WA 98195, USA.
June L RoundDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, 4280 JMRB, 15 North Medical Dr. East, Salt Lake City, UT 84112, USA.
Ryan M O'ConnellDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, 4280 JMRB, 15 North Medical Dr. East, Salt Lake City, UT 84112, USA. Electronic address: ryan.oconnell@path.utah.edu.
University of Utah · USUniversity of Washington · USUniversity of California, Los Angeles · US

Funding

RESEARCH TRAINING IN HEMATOLOGYT32DK007115 · NIDDK · UNIVERSITY OF UTAH · PI LEIBOLD, ELIZABETH ANN, PRCHAL, JOSEF T · 1986 to 2020
$8.4M
Characterizing tumor suppressive functions of microRNAs in B-cell neoplasiaR01CA166450 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI RAO, DINESH S · 2013 to 2017
$2.5M
Utilizing TALEN technology to regulate human microRNA'sDP2GM111099 · NIGMS · UNIVERSITY OF UTAH · PI O'CONNELL, RYAN M · 2013 to 2013
$2.2M
Role of B-cell oncogenes and microRNA-34 in B-lymphopoiesis and neoplasiaK08CA133521 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI RAO, DINESH S · 2009 to 2013
$784k
Investigate the Role of Micro-RNA 155 in Myeloid Development during InflammationR00HL102228 · NHLBI · UNIVERSITY OF UTAH · PI O'CONNELL, RYAN M · 2011 to 2013
$654k
The role of T cell intrinsic TLR signaling on host-commensal interactionsR56AI107090 · NIAID · UNIVERSITY OF UTAH · PI ROUND, JUNE LOUISE · 2013 to 2013
$350k
Exploring the mechanisms of T cell intrinsic TLR2 signaling on Treg functionK22AI095375 · NIAID · UNIVERSITY OF UTAH · PI ROUND, JUNE LOUISE · 2012 to 2013
$270k
Generation and initial charcterization of a mouse with floxed miR-155 for conditiR03NS070141 · NINDS · UNIVERSITY OF WASHINGTON · PI GARDEN, GWENN A · 2010 to 2011
$154k
NCCDPHP CDC HHS DP2GM111099-01NCI NIH HHS K08 CA133521NCI NIH HHS R01 CA166450NCI NIH HHS R01CA166450-02NHLBI NIH HHS R00 HL102228NHLBI NIH HHS R00HL102228-05NIAID NIH HHS AI107090NIAID NIH HHS K22 AI095375NIAID NIH HHS K22 AI95375NIAID NIH HHS R56 AI107090NIDDK NIH HHS 5T32DK007115-39NIDDK NIH HHS T32 DK007115NIGMS NIH HHS DP2 GM111099NINDS NIH HHS R03 NS070141NINDS NIH HHS R03NS070141
6 · The paper itself

Abstract

Chronic inflammation is a contributing factor to most life-shortening human diseases. However, the molecular and cellular mechanisms that sustain chronic inflammatory responses remain poorly understood, making it difficult to treat this deleterious condition. Using a mouse model of age-dependent inflammation that results from a deficiency in miR-146a, we demonstrate that miR-155 contributed to the progressive inflammatory disease that emerged as Mir146a(-/-) mice grew older. Upon analyzing lymphocytes from inflamed versus healthy middle-aged mice, we found elevated numbers of T follicular helper (Tfh) cells, germinal center (GC) B cells, and autoantibodies, all occurring in a miR-155-dependent manner. Further, Cd4-cre Mir155(fl/fl) mice were generated and demonstrated that miR-155 functions in T cells, in addition to its established role in B cells, to promote humoral immunity in a variety of contexts. Taken together, our study discovers that miR-146a and miR-155 counterregulate Tfh cell development that drives aberrant GC reactions during chronic inflammation.

Indexed as

Adoptive TransferAnimalsAutoantibodiesB-LymphocytesCD4 AntigensCell DifferentiationDisease Models, AnimalFos-Related Antigen-2Germinal CenterImmunity, HumoralInflammationLymphocyte ActivationMiceMice, Inbred C57BLMice, KnockoutMicroRNAsAutoantibodiesCD4 AntigensFosl2 protein, mouseFos-Related Antigen-2MicroRNAsMirn146 microRNA, mouseMirn155 microRNA, mouseRNA, Small Interfering

Identifiers

PMID25367574
PMCPMC4657560
OpenAlexW2141875386

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.