Evidence map›Paper›PMID 28550121›Full record

ArticleJournal of leukocyte biology2017

BCL6 represses antiviral resistance in follicular T helper cells.

Tohti Amet, Young Min Son, Li Jiang, In Su Cheon, Su Huang, Samir K Gupta, Alexander L Dent, Luis J Montaner, Qigui Yu, Jie Sun

Open access · bronzeAbstract read
In one paragraph

Article in Journal of leukocyte biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 25 citations in OpenAlex.

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  13. TFrontiers in immunology · 2020
    Article
  14. Review
  15. Article
  16. CD4AIDS research and human retroviruses · 2018
    Review
  17. Article
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  19. Review
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

10 authors at 4 institutions in 1 country.

Tohti AmetDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Young Min SonDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Li JiangDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
In Su CheonDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Su HuangDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Samir K GuptaDepartment of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Alexander L DentDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Luis J MontanerWistar Institute, Philadelphia, Pennsylvania, USA; and.
Qigui YuDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Jie SunDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, USA; sun.jie@mayo.edu.
Indiana University – Purdue University Indianapolis · USIndiana University School of MedicineMayo Clinic · USThe Wistar Institute · US

Funding

First-in-human study of two anti-SARS CoV-2 antibodies in health volunteersUM1AI126620 · NIAID · WISTAR INSTITUTE · PI MONTANER, LUIS J, RILEY, JAMES L. · 2016 to 2021
$24.5M
Towards Eradication: Reducing Proviral HIV DNA with Interferon-α ImmunotherapyU01AI110434 · NIAID · WISTAR INSTITUTE · PI MONTANER, LUIS J · 2014 to 2017
$7.2M
Molecular regulation of protective CD8 immunity against influenza infectionR01AI112844 · NIAID · UNIVERSITY OF VIRGINIA · PI SUN, JIE · 2015 to 2024
$4.5M
Early Innate/IgA Anti-HIV/SIV Response in Exposed UninfectedR01AI094603 · NIAID · WISTAR INSTITUTE · PI KRAISELBURD, EDMUNDO NELSON, MONTANER, LUIS J · 2011 to 2015
$3.8M
Regulation of pulmonary anti-viral immunity in normal and obese hostsR01HL126647 · NHLBI · MAYO CLINIC ROCHESTER · PI SUN, JIE · 2015 to 2019
$1.9M
Targeting latently infected Tfh cells to achieving a functional cure of HIV-1R01AI117835 · NIAID · INDIANA UNIVERSITY INDIANAPOLIS · PI YU, QIGUI A. · 2015 to 2019
$1.9M
Simultaneously boosting both humoral and cellular immunity following vaccinationR01AG047156 · NIA · MAYO CLINIC ROCHESTER · PI SUN, JIE · 2015 to 2019
$1.6M
Specific killing of latently HIV-1-infected cells after provirus reactivationR33AI104268 · NIAID · INDIANA UNIVERSITY INDIANAPOLIS · PI YU, QIGUI A. · 2015 to 2017
$1.2M
Targeting macrophage Bcl6 to enhance innate resistance to influenzaR21AI119612 · NIAID · MAYO CLINIC ROCHESTER · PI SUN, JIE · 2015 to 2016
$446k
NHLBI NIH HHS R01 HL126647NIAID NIH HHS R01 AI094603NIAID NIH HHS R01 AI112844NIAID NIH HHS R01 AI117835NIAID NIH HHS R21 AI119612NIAID NIH HHS R33 AI104268NIAID NIH HHS U01 AI110434NIAID NIH HHS UM1 AI126620NIA NIH HHS R01 AG047156
6 · The paper itself

Abstract

Follicular Th (Tfh) cells are a distinct subset of Th cells that help B cells produce class-switched antibodies. Studies have demonstrated that Tfh cells are highly prone to HIV infection and replication. However, the molecular mechanisms underlying this phenomenon are largely unclear. Here, we show that murine and human Tfh cells have diminished constitutive expression of IFN-stimulated genes (ISGs) inclusive of antiviral resistance factor MX dynamin-like GTPase 2 (MX2) and IFN-induced transmembrane 3 (IFITM3) compared with non-Tfh cells. A lower antiviral resistance in Tfh was consistent with a higher susceptibility to retroviral infections. Mechanistically, we found that BCL6, a master regulator of Tfh cell development, binds to ISG loci and inhibits the expression of MX2 and IFITM3 in Tfh cells. We demonstrate further that inhibition of the BCL6 BR-C, ttk, and bab (BTB) domain function increases the expression of ISGs and suppresses HIV infection and replication in Tfh cells. Our data reveal a regulatory role of BCL6 in inhibiting antiviral resistance factors in Tfh cells, thereby promoting the susceptibility Tfh cells to viral infections. Our results indicate that the modulation of BCL6 function in Tfh cells could be a potential strategy to enhance Tfh cell resistance to retroviral infections and potentially decrease cellular reservoirs of HIV infection.

Indexed as

AnimalsBlotting, WesternCell LineChromatin ImmunoprecipitationDisease ResistanceFlow CytometryHIV-1HIV InfectionsHumansMiceMice, Inbred C57BLProto-Oncogene Proteins c-bcl-6Real-Time Polymerase Chain ReactionT-Lymphocytes, Helper-InducerBCL6 protein, humanBcl6 protein, mouseProto-Oncogene Proteins c-bcl-6HIV infectionIFITM3MX2Tfh cell

Identifiers

PMID28550121
PMCPMC5505751
OpenAlexW2618163258

What OpenQuestion holds

Textmetadata
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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.