Evidence map›Paper›PMID 39492991›Full record

ArticleFrontiers in cellular and infection microbiology2024

Single-stranded DNA oligonucleotides containing CpG motifs are non-stimulatory

Andrew Scott, Benjamin Farrar, Tom Young, Joann Prior, Chad Stratilo, Leonie Unterholzner, Riccardo D'Elia

Abstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Andrew ScottMicrobiology, Defence Science and Technology Laboratory, Salisbury, United Kingdom.
Benjamin FarrarMicrobiology, Defence Science and Technology Laboratory, Salisbury, United Kingdom.
Tom YoungDivision of Biomedical and Life Sciences, Faculty of Health and Medicine, Lancaster University, Lancaster, United Kingdom.
Joann PriorMicrobiology, Defence Science and Technology Laboratory, Salisbury, United Kingdom.
Chad StratiloBio Threat Defence Section, Defence Research and Development Canada, Ralston, AB, Canada.
Leonie UnterholznerDivision of Biomedical and Life Sciences, Faculty of Health and Medicine, Lancaster University, Lancaster, United Kingdom.
Riccardo D'EliaMicrobiology, Defence Science and Technology Laboratory, Salisbury, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Therapies that modulate and appropriately direct the immune response are promising candidates for the treatment of infectious diseases. One such candidate therapeutic is DZ13, a short, synthetic, single-stranded DNA molecule. This molecule has enzymatic activity and can modulate the immune response by binding to and degrading the mRNA encoding a key immuno-regulatory molecule. Originally developed and entering clinical trials as an anti-cancer agent, DZ13 has also been evaluated as a treatment for viral infections, and has been shown to provide protection against infection with influenza virus in a mouse model of infection. In this work, we evaluated whether the immuno-modulatory properties of DZ13 could provide protection against the potential biothreat pathogen

Indexed as

Burkholderia pseudomalleiDisease Models, AnimalDNA, Single-StrandedMelioidosisOligodeoxyribonucleotidesAnimalsFemaleImmunologic FactorsMiceMice, Inbred BALB CCPG-oligonucleotideDNA, Single-StrandedImmunologic FactorsOligodeoxyribonucleotidesanti-inflammatoryBurkholderia pseudomalleiCpGDNAzymemelioidosis

Identifiers

PMID39492991
PMCPMC11527787

What OpenQuestion holds

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LicenceCC BY
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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.