Evidence map›Paper›PMID 38744279›Full record

ArticleCell reports. Medicine2024

Uncoupling interferons and the interferon signature explains clinical and transcriptional subsets in SLE.

Eduardo Gómez-Bañuelos, Daniel W Goldman, Victoria Andrade, Erika Darrah, Michelle Petri, Felipe Andrade

Abstract read
In one paragraph

Article in Cell reports. Medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Eduardo Gómez-BañuelosDivision of Rheumatology, The Johns Hopkins School of Medicine, Baltimore, MD 21224. Electronic address: jgomezb1@jhmi.edu.
Daniel W GoldmanDivision of Rheumatology, The Johns Hopkins School of Medicine, Baltimore, MD 21224.
Victoria AndradeDivision of Rheumatology, The Johns Hopkins School of Medicine, Baltimore, MD 21224.
Erika DarrahDivision of Rheumatology, The Johns Hopkins School of Medicine, Baltimore, MD 21224.
Michelle PetriDivision of Rheumatology, The Johns Hopkins School of Medicine, Baltimore, MD 21224.
Felipe AndradeDivision of Rheumatology, The Johns Hopkins School of Medicine, Baltimore, MD 21224. Electronic address: andrade@jhmi.edu.

Funding

Hopkins Lupus CohortR01AR069572 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI PETRI, MICHELLE A · 2016 to 2020
$3.4M
Autoimmunity to LINE-1-encoded antigens in SLE pathogenesisR21AI147598 · NIAID · JOHNS HOPKINS UNIVERSITY · PI ANDRADE, FELIPE · 2020 to 2021
$450k
Transcription factor A mitochondria in SLE pathogenesisR21AI169851 · NIAID · JOHNS HOPKINS UNIVERSITY · PI ANDRADE, FELIPE · 2022 to 2023
$450k
LINE1-ORF0 in SLE pathogenesisR21AI176766 · NIAID · JOHNS HOPKINS UNIVERSITY · PI ANDRADE, FELIPE · 2023 to 2024
$450k
NIAID NIH HHS R21 AI147598NIAID NIH HHS R21 AI169851NIAID NIH HHS R21 AI176766NIAMS NIH HHS R01 AR069572
6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE) displays a hallmark interferon (IFN) signature. Yet, clinical trials targeting type I IFN (IFN-I) have shown variable efficacy, and blocking IFN-II failed to treat SLE. Here, we show that IFN type levels in SLE vary significantly across clinical and transcriptional endotypes. Whereas skin involvement correlated with IFN-I alone, systemic features like nephritis associated with co-elevation of IFN-I, IFN-II, and IFN-III, indicating additive IFN effects in severe SLE. Notably, while high IFN-II/-III levels without IFN-I had a limited effect on disease activity, IFN-II was linked to IFN-I-independent transcriptional profiles (e.g., OXPHOS and CD8

Indexed as

InterferonsLupus Erythematosus, SystemicAdultFemaleGene Expression RegulationHumansInterferon Type IMaleMiddle AgedTranscription, GeneticTranscriptomeInterferonsInterferon Type Iinterferoninterferon signaturesystemic lupus erythematosus

Identifiers

PMID38744279
PMCPMC11148857

What OpenQuestion holds

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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.