Evidence map›Paper›PMID 32860771›Full record

ReviewJournal of molecular biology2020

Animal Models for the Study of Nucleic Acid Immunity: Novel Tools and New Perspectives.

Isabelle K Vila, Maxence Fretaud, Dimitrios Vlachakis, Nadine Laguette, Christelle Langevin

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of molecular biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Frontiers in immunology · 2021
    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 5 institutions in 2 countries.

Isabelle K VilaInstitut de Génétique Humaine, CNRS, Université de Montpellier, Molecular Basis of Inflammation Laboratory, Montpellier, France. Electronic address: isabelle.vila@igh.cnrs.fr.
Maxence FretaudUniversité Paris-Saclay, INRAE, UVSQ, VIM, 78350 Jouy-en-Josas, France.
Dimitrios VlachakisLaboratory of Genetics, Department of Biotechnology, School of Applied Biology and Biotechnology, Agricultural University of Athens, 75 Iera Odos, 11855 Athens, Greece; Division of Endocrinology and Metabolism, Center of Clinical, Experimental Surgery and Translational Research, Biomedical Research Foundation of the Academy of Athens, 11527 Athens, Greece; University Research Institute of Maternal and Child Health & Precision Medicine, Medical School, National and Kapodistrian University of Athens, 11527 Athens, Greece.
Nadine LaguetteInstitut de Génétique Humaine, CNRS, Université de Montpellier, Molecular Basis of Inflammation Laboratory, Montpellier, France.
Christelle LangevinUniversité Paris-Saclay, INRAE, IERP, 78350 Jouy-en-Josas, France. Electronic address: christelle.langevin@inrae.fr.
Biomedical Research Foundation of the Academy of Athens · GRInstitut de Génétique Humaine · FRInstitut de Génétique Moléculaire de Montpellier · FRInstitut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement · FRVirologie et Immunologie Moléculaires · FR

Funding

European Research Council 637763
6 · The paper itself

Abstract

Unresolved inflammation fosters and supports a wide range of human pathologies. There is growing evidence for a role played by cytosolic nucleic acids in initiating and supporting pathological chronic inflammation. In particular, the cGAS-STING pathway has emerged as central to the mounting of nucleic acid-dependent type I interferon responses, leading to the identification of small-molecule modulators of STING that have raised clinical interest. However, several new challenges have emerged, representing potential obstacles to efficient clinical translation. Indeed, the current literature underscores that nucleic acid-induced inflammatory responses are subjected to several layers of regulation, further suggesting complex coordination at the cell-type, tissue or organism level. Untangling the underlying processes is paramount to the identification of specific therapeutic strategies targeting deleterious inflammation. Herein, we present an overview of human pathologies presenting with deregulated interferon levels and with accumulation of cytosolic nucleic acids. We focus on the central role of the STING adaptor protein in these pathologies and discuss how in vivo models have forged our current understanding of nucleic acid immunity. We present our opinion on the advantages and limitations of zebrafish and mice models to highlight their complementarity for the study of inflammatory human pathologies and the development of therapeutics. Finally, we discuss high-throughput screening strategies that generate multi-parametric datasets that allow integrative analysis of heterogeneous information (imaging and omics approaches). These approaches are likely to structure the future of screening strategies for the treatment of human pathologies.

Indexed as

ImmunityModels, AnimalAnimalsAntiviral AgentsCytosolDNA, ViralDrug Evaluation, PreclinicalEvolution, MolecularHigh-Throughput Screening AssaysImmunity, InnateInflammationInterferon Type IMembrane ProteinsMiceMutationNucleic AcidsAntiviral AgentsDNA, ViralInterferon Type IMembrane ProteinsNucleic AcidsNucleotidyltransferasesdrug screeninginflammatory modelsinnate immunityinterferon signalingSTING

Identifiers

PMID32860771
PMCPMC7611023
OpenAlexW3082104374

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.