Evidence map›Paper›PMID 39057915›Full record

ArticleInfection and immunity2024

ER-transiting bacterial toxins amplify STING innate immune responses and elicit ER stress.

Catherine Schlenker, Katharina Richard, Sofia Skobelkina, R Paige Mathena, Darren J Perkins

Abstract read
In one paragraph

Article in Infection and immunity, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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

5 authors.

Catherine SchlenkerProgram in Oncology University of Maryland, Baltimore (UMB), School of Medicine , Baltimore, Maryland, USA.
Katharina RichardDepartment of Microbiology and Immunology, School of Medicine , Baltimore, Maryland, USA.
Sofia SkobelkinaProgram in Oncology University of Maryland, Baltimore (UMB), School of Medicine , Baltimore, Maryland, USA.
R Paige MathenaDepartment of Microbiology and Immunology, School of Medicine , Baltimore, Maryland, USA.
Darren J PerkinsProgram in Oncology University of Maryland, Baltimore (UMB), School of Medicine , Baltimore, Maryland, USA.ORCID 0000-0003-1368-6366

Funding

PGE2 Receptor Regulation of TLR4/TRIF Responses to Bacterial InfectionR21AI151352 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI PERKINS, DARREN · 2020 to 2021
$425k
PGE2 Receptor Suppression of cGAS/STING Responses in anti-tumor immunityR21AI152051 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI PERKINS, DARREN · 2020 to 2021
$425k
American Cancer Society (ACS) IRG-18-160-16.HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) R21AI152051,R21AI151352NIAID NIH HHS R21 AI151352NIAID NIH HHS R21 AI152051The State of Maryland | Maryland Department of Health (DHMH) CH-649-CRF
6 · The paper itself

Abstract

The cGAS/STING sensor system drives innate immune responses to intracellular microbial double-stranded DNA (dsDNA) and bacterial cyclic nucleotide second messengers (e.g., c-di-AMP). STING-dependent cell-intrinsic responses can increase resistance to microbial infection and speed pathogen clearance. Correspondingly, STING activation and signaling are known to be targeted for suppression by effectors from several bacterial pathogens. Whether STING responses are also positively regulated through sensing of specific bacterial effectors is less clear. We find that STING activation through dsDNA, by its canonical ligand 2'-3' cGAMP, or the small molecule DMXAA is potentiated following intracellular delivery of the AB

Indexed as

Bacterial ToxinsEndoplasmic Reticulum StressImmunity, InnateMembrane ProteinsAnimalsEndoplasmic ReticulumHumansMacrophagesMiceMice, Inbred C57BLSignal TransductionSTING ProteinBacterial ToxinsMembrane ProteinsSting1 protein, mouseSTING ProteinADP ribosylationcGAScholera toxinendoplasmic reticulumGPCRpertussis toxinSTINGtype I interferon

Identifiers

PMID39057915
PMCPMC11321001

What OpenQuestion holds

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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.