Evidence map›Paper›PMID 30692590›Full record

ArticleScientific reports2019

Both anti-inflammatory and antiviral properties of novel drug candidate ABX464 are mediated by modulation of RNA splicing.

Audrey Vautrin, Laurent Manchon, Aude Garcel, Noëlie Campos, Laure Lapasset, Abdelhamid Mahdi Laaref, Roman Bruno, Marie Gislard, Emeric Dubois, Didier Scherrer and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

39 citing papers in PubMed, 62 citations in OpenAlex.

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  20. miRNA Molecules-Late Breaking Treatment for Inflammatory Bowel Diseases?International journal of molecular sciences · 2023
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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

12 authors at 3 institutions in 1 country.

Audrey VautrinABIVAX, 1919 route de Mende, 34293, Montpellier Cedex 5, Montpellier, France.
Laurent ManchonIGMM, CNRS, Univ. Montpellier, Montpellier, France.
Aude GarcelABIVAX, 1919 route de Mende, 34293, Montpellier Cedex 5, Montpellier, France.
Noëlie CamposABIVAX, 1919 route de Mende, 34293, Montpellier Cedex 5, Montpellier, France.
Laure LapassetABIVAX, 1919 route de Mende, 34293, Montpellier Cedex 5, Montpellier, France.
Abdelhamid Mahdi LaarefIGMM, CNRS, Univ. Montpellier, Montpellier, France.
Roman BrunoACOBIOM, 1682 Rue de la Valsière, 34184, Montpellier Cedex 4, Montpellier, France.
Marie GislardMGX, Univ Montpellier, CNRS, INSERM, Montpellier, France.
Emeric DuboisMGX, Univ Montpellier, CNRS, INSERM, Montpellier, France.ORCID 0000-0002-6052-4178
Didier ScherrerABIVAX, 1919 route de Mende, 34293, Montpellier Cedex 5, Montpellier, France.
J Hartmut EhrlichABIVAX, 1919 route de Mende, 34293, Montpellier Cedex 5, Montpellier, France.
Jamal TaziIGMM, CNRS, Univ. Montpellier, Montpellier, France. jamal.tazi@igmm.cnrs.fr.
Abivax (France) · FRCentre National de la Recherche Scientifique · FRAcobiom (France) · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ABX464 is a first-in-class, clinical-stage, small molecule for oral administration that has shown strong anti-inflammatory effects in the DSS-model for inflammatory bowel disease (IBD) and also prevents replication of the HIV virus. ABX464 which binds to cap binding complex (CBC) has demonstrated safety and efficacy in a phase 2a proof-of-concept clinical trial in patients with Ulcerative colitis. Previously, with limited technologies, it was not possible to quantify the effect of ABX464 on viral and cellular RNA biogenesis. Here, using RNA CaptureSeq and deep sequencing, we report that ABX464 enhances the splicing of HIV RNA in infected PBMCs from six healthy individuals and also the expression and splicing of a single long noncoding RNA to generate the anti-inflammatory miR-124 both ex vivo and in HIV patients. While ABX464 has no effect on pre-mRNA splicing of cellular genes, depletion of CBC complex by RNAi leads to accumulation of intron retention transcripts. These results imply that ABX464 did not inhibit the function of CBC in splicing but rather strengthens it under pathological condition like inflammation and HIV infection. The specific dual ability of ABX464 to generate both anti-inflammatory miR-124 and spliced viral RNA may have applicability for the treatment of both inflammatory diseases and HIV infection.

Indexed as

Anti-HIV AgentsAnti-Inflammatory AgentsCells, CulturedGene Expression RegulationHeLa CellsHigh-Throughput Nucleotide SequencingHIVHumansLeukocytes, MononuclearMicroRNAsQuinolinesRNA SplicingRNA, ViralSequence Analysis, RNAABX464Anti-HIV AgentsAnti-Inflammatory AgentsMicroRNAsMIRN124 microRNA, humanQuinolinesRNA, Viral

Identifiers

PMID30692590
PMCPMC6349857
OpenAlexW2914778798

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.