Evidence map›Paper›PMID 33046502›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2020

Adenosine-to-Inosine RNA Editing of Alu Double-Stranded (ds)RNAs Is Markedly Decreased in Multiple Sclerosis and Unedited Alu dsRNAs Are Potent Activators of Proinflammatory Transcriptional Responses.

John T Tossberg, Rachel M Heinrich, Virginia M Farley, Philip S Crooke, Thomas M Aune

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.4field-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

23 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
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  4. Review
  5. Deaminase Modulation Driving a New Era in Drug Development.International journal of molecular sciences · 2025
    Review
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  11. Global medical genetics · 2023
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

5 authors at 2 institutions in 1 country.

John T TossbergDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN 37212.
Rachel M HeinrichDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN 37212.
Virginia M FarleyDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN 37212.
Philip S CrookeDepartment of Mathematics, Vanderbilt University, Nashville, TN 37212; and.
Thomas M AuneDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN 37212; tom.aune@vumc.org.ORCID 0000-0002-4968-4306
Vanderbilt University Medical Center · USVanderbilt University · US

Funding

IFN GAMMA GENE REGULATION IN T CELLS AND NK CELLSR01AI044924 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI AUNE, THOMAS M. · 2000 to 2019
$5.8M
Alu RNAs and double-stranded RNA sensorsR21AI144193 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI AUNE, THOMAS M. · 2019 to 2020
$468k
IFN-Gamma Gene Regulation in T Cells and NK CellsR56AI044924 · NIAID · VANDERBILT UNIVERSITY · PI AUNE, THOMAS M. · 2009 to 2009
$349k
NIAID NIH HHS R01 AI044924NIAID NIH HHS R21 AI144193NIAID NIH HHS R56 AI044924
6 · The paper itself

Abstract

Sensors that detect dsRNA stimulate IFN responses as a defense against viral infection. IFN responses are also well documented in a variety of human autoimmune diseases, including relapsing-remitting multiple sclerosis (MS), in which increased IFN responses result from increased levels of double-stranded endogenous Alu RNAs. Mechanisms underlying increases in double-stranded Alu RNAs in MS are obscure. We find widespread loss of adenosine-to-inosine editing of Alu RNAs in MS. Unedited Alu RNAs are potent activators of both IFN and NF-κB responses via the dsRNA sensors, RIG-I, and TLR3. Minor editing of highly active Alu elements abrogates the ability to activate both transcriptional responses. Thus, adenosine-to-inosine editing may also represent an important defense against autoimmune diseases such as MS.

Indexed as

AdenosineAlu ElementsDatasets as TopicDEAD Box Protein 58HEK293 CellsHumansInflammationInosineInterferonsMultiple Sclerosis, Relapsing-RemittingNF-kappa BReceptors, ImmunologicRNA, Double-StrandedRNA EditingRNA-SeqSignal TransductionAdenosineDEAD Box Protein 58InosineInterferonsNF-kappa BReceptors, ImmunologicRIGI protein, humanRNA, Double-StrandedTLR3 protein, humanToll-Like Receptor 3

Identifiers

PMID33046502
PMCPMC7872017
OpenAlexW3092171245

What OpenQuestion holds

Textmetadata
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.