Evidence map›Paper›PMID 34346769›Full record

ArticleJournal of virology2021

T Cell-Intrinsic Interferon Regulatory Factor 1 Expression Suppresses Differentiation of CD4

C N Jondle, K E Johnson, W P Mboko, V L Tarakanova

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
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

4 authors at 1 institution in 1 country.

C N JondleDepartment of Microbiology and Immunology, Medical College of Wisconsingrid.30760.32, Milwaukee, Wisconsin, USA.
K E JohnsonDepartment of Microbiology and Immunology, Medical College of Wisconsingrid.30760.32, Milwaukee, Wisconsin, USA.
W P MbokoDepartment of Microbiology and Immunology, Medical College of Wisconsingrid.30760.32, Milwaukee, Wisconsin, USA.
V L TarakanovaDepartment of Microbiology and Immunology, Medical College of Wisconsingrid.30760.32, Milwaukee, Wisconsin, USA.ORCID 0000-0002-9499-088X
Medical College of Wisconsin · US

Funding

IRF-1: a brake to limit gammaherpesvirus infection and pathogenesisR01CA203923 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI TARAKANOVA, VERA L. · 2017 to 2021
$2.0M
Not just acute: IRF-7 has two site-specific functions against chronic gammaherpesvirus infectionF31CA243364 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI JOHNSON, KAITLIN E · 2019 to 2020
$45k
American Cancer Society (ACS) 134165-PF-19-176-01-MPCHHS | NIH | National Cancer Institute (NCI) CA203923HHS | NIH | National Cancer Institute (NCI) CA243364NCI NIH HHS F31 CA243364NCI NIH HHS R01 CA203923
6 · The paper itself

Abstract

Gammaherpesviruses are ubiquitous pathogens that establish lifelong infection and are associated with B cell lymphomas. To establish chronic infection, these viruses usurp B cell differentiation and drive a robust germinal center response to expand the latent viral reservoir and gain access to memory B cells. Germinal center B cells, while important for the establishment of latent infection, are also thought to be the target of viral transformation. The host and viral factors that impact the gammaherpesvirus-driven germinal center response are not clearly defined. We show that the global expression of the antiviral and tumor suppressor interferon regulatory factor 1 (IRF-1) selectively attenuates the murine gammaherpesvirus 68 (MHV68)-driven germinal center response and restricts the expansion of the latent viral reservoir. In this study, we found that T cell-intrinsic IRF-1 expression recapitulates some aspects of the antiviral state imposed by IRF-1 during chronic MHV68 infection, including the attenuation of the germinal center response and viral latency in the spleen. We also discovered that global and T cell-intrinsic IRF-1 deficiency leads to an unhindered rise of interleukin-17A (IL-17A)-expressing and follicular helper T cell populations, two CD4

Indexed as

AnimalsB-LymphocytesCD4-Positive T-LymphocytesCell DifferentiationFemaleGammaherpesvirinaeGerminal CenterHerpesviridae InfectionsHost-Pathogen InteractionsInterferon Regulatory Factor-1Interleukin-17Lymphocyte ActivationMaleMiceMice, Inbred C57BLMice, KnockoutInterferon Regulatory Factor-1Interleukin-17chronic infectiongammaherpesvirusgerminal centerIL-17AIRF-1T cellT follicular helper

Identifiers

PMID34346769
PMCPMC8475519
OpenAlexW3188440024

What OpenQuestion holds

Textmetadata
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.