Evidence map›Paper›PMID 30013024›Full record

ArticleNature communications2018

Differential cell-intrinsic regulations of germinal center B and T cells by miR-146a and miR-146b.

Sunglim Cho, Hyang-Mi Lee, I-Shing Yu, Youn Soo Choi, Hsi-Yuan Huang, Somaye Sadat Hashemifar, Ling-Li Lin, Mei-Chi Chen, Nikita D Afanasiev, Aly Azeem Khan and 4 more

Abstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
–field-weighted citation impact
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

48 citing papers in PubMed.

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  13. SilencingBiomolecules · 2023
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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.

Sunglim ChoDivision of Biological Sciences, University of California, La Jolla, San Diego, CA, 92093, USA.ORCID http://orcid.org/0000-0003-3109-0216
Hyang-Mi LeeDivision of Biological Sciences, University of California, La Jolla, San Diego, CA, 92093, USA.
I-Shing YuLaboratory Animal Center, College of Medicine, National Taiwan University, Taipei, 100, Taiwan.ORCID http://orcid.org/0000-0002-2369-5816
Youn Soo ChoiDivision of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla, CA, 92037, USA.
Hsi-Yuan HuangDepartment of Laboratory Medicine, China Medical University Hospital, China Medical University, Taichung, Taiwan.
Somaye Sadat HashemifarToyota Technological Institute, Chicago, IL, 60637, USA.
Ling-Li LinDivision of Biological Sciences, University of California, La Jolla, San Diego, CA, 92093, USA.
Mei-Chi ChenDivision of Biological Sciences, University of California, La Jolla, San Diego, CA, 92093, USA.
Nikita D AfanasievDivision of Biological Sciences, University of California, La Jolla, San Diego, CA, 92093, USA.
Aly Azeem KhanToyota Technological Institute, Chicago, IL, 60637, USA.
Shu-Wha LinDepartment of Clinical Laboratory Sciences and Medical Biotechnology, College of Medicine, National Taiwan University, Taipei, 100, Taiwan.
Alexander Y RudenskyHoward Hughes Medical Institute and Immunology Program, Ludwig Center at Memorial Sloan-Kettering Cancer Center, Memorial Sloan-Kettering Cancer Center, New York, NY, 10065, USA.
Shane CrottyDivision of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla, CA, 92037, USA.ORCID http://orcid.org/0000-0002-6484-6262
Li-Fan LuDivision of Biological Sciences, University of California, La Jolla, San Diego, CA, 92093, USA. lifanlu@ucsd.edu.ORCID http://orcid.org/0000-0002-9727-0036

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Role of microRNAs in regulatory T cell-mediated immunological tolerance and T celR01AI108651 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LU, LI-FAN · 2014 to 2024
$4.0M
Function of microRNAs in controlling regulatory T cell biologyR00AI089935 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LU, LI-FAN · 2012 to 2013
$493k
The role of SOCS1 repression by miR-155 in regulating immune responsivenessR21AI103646 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LU, LI-FAN · 2013 to 2014
$426k
Role of miR-146a at the interface between T and B cell immunityR21AI123782 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LU, LI-FAN · 2016 to 2017
$420k
Function of microRNAs in controlling regulatory T cell biologyK99AI089935 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI LU, LI-FAN · 2011 to 2011
$94k
NCI NIH HHS P30 CA008748NIAID NIH HHS K99 AI089935NIAID NIH HHS R00 AI089935NIAID NIH HHS R01 AI108651NIAID NIH HHS R21 AI103646NIAID NIH HHS R21 AI123782U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AI089935U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AI103646U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AI108651U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AI123782
6 · The paper itself

Abstract

Reciprocal interactions between B and follicular T helper (Tfh) cells orchestrate the germinal center (GC) reaction, a hallmark of humoral immunity. Abnormal GC responses could lead to the production of pathogenic autoantibodies and the development of autoimmunity. Here we show that miR-146a controls GC responses by targeting multiple CD40 signaling pathway components in B cells; by contrast, loss of miR-146a in T cells does not alter humoral responses. However, specific deletion of both miR-146a and its paralog, miR-146b, in T cells increases Tfh cell numbers and enhanced GC reactions. Thus, our data reveal differential cell-intrinsic regulations of GC B and Tfh cells by miR-146a and miR-146b. Together, members of the miR-146 family serve as crucial molecular brakes to coordinately control GC reactions to generate protective humoral responses without eliciting unwanted autoimmunity.

Indexed as

AnimalsAutoantibodiesAutoimmunityB-LymphocytesBone Marrow CellsCD40 AntigensCell DifferentiationGene Expression RegulationGerminal CenterImmunity, HumoralInterleukin-4MiceMice, TransgenicMicroRNAsPrimary Cell CultureProtein IsoformsAutoantibodiesCD40 AntigensInterleukin-4MicroRNAsMirn146 microRNA, mouseProtein Isoforms

Identifiers

PMID30013024
PMCPMC6048122

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Registered trials

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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.