Evidence map›Paper›PMID 35293862›Full record

ArticleeLife2022

Targeting the Annexin A1-FPR2/ALX pathway for host-directed therapy in dengue disease.

Vivian Vasconcelos Costa, Michelle A Sugimoto, Josy Hubner, Caio S Bonilha, Celso Martins Queiroz-Junior, Marcela Helena Gonçalves-Pereira, Jianmin Chen, Thomas Gobbetti, Gisele Olinto Libanio Rodrigues, Jordana L Bambirra and 12 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.7field-weighted citation impact, top 5% 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

19 citing papers in PubMed, 46 citations in OpenAlex.

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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

22 authors at 4 institutions in 4 countries.

Vivian Vasconcelos Costa *Department of Morphology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.ORCID 0000-0002-0175-642X
Michelle A Sugimoto *Department of Biochemistry and Immunology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.ORCID 0000-0002-4527-6065
Josy HubnerDepartment of Morphology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Caio S BonilhaDepartment of Biochemistry and Immunology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Celso Martins Queiroz-JuniorDepartment of Morphology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Marcela Helena Gonçalves-PereiraDepartment of Biochemistry and Immunology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Jianmin ChenWilliam Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
Thomas GobbettiWilliam Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
Gisele Olinto Libanio RodriguesDepartment of Biochemistry and Immunology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Jordana L BambirraDepartment of Microbiology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Ingredy B PassosDepartment of Morphology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Carla Elizabeth Machado LopesDepartment of Morphology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Thaiane P MoreiraDepartment of Microbiology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Kennedy BonjourDepartment of Biology, Institute of Biological Sciences, Federal University of Juiz de Fora, Juiz de Fora, Brazil.
Rossana C N MeloDepartment of Biology, Institute of Biological Sciences, Federal University of Juiz de Fora, Juiz de Fora, Brazil.
Milton A P OliveiraTropical Pathology and Public Health Institute, Universidade Federal de Goiás, Goiânia, Brazil.
Marcus Vinicius M AndradeSchool of Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Lirlândia Pires SousaDepartment of Clinical and Toxicological Analyses, School of Pharmacy, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.ORCID 0000-0002-1042-9762
Danielle Gloria SouzaDepartment of Microbiology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Helton da Costa SantiagoDepartment of Biochemistry and Immunology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Mauro Perretti *William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.ORCID 0000-0003-2068-3331
Mauro Martins Teixeira *Department of Biochemistry and Immunology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.ORCID 0000-0002-6944-3008
Universidade Federal de Minas Gerais · BRQueen Mary University of London · GBUniversidade Federal de Juiz de Fora · BRPublic Health Institute · US

Funding

Medical Research Council MR/N017544/1Medical Research Council MR/NO17544/1
6 · The paper itself

Abstract

Host immune responses contribute to dengue's pathogenesis and severity, yet the possibility that failure in endogenous inflammation resolution pathways could characterise the disease has not been contemplated. The pro-resolving protein Annexin A1 (AnxA1) is known to counterbalance overexuberant inflammation and mast cell (MC) activation. We hypothesised that inadequate AnxA1 engagement underlies the cytokine storm and vascular pathologies associated with dengue disease. Levels of AnxA1 were examined in the plasma of dengue patients and infected mice. Immunocompetent, interferon (alpha and beta) receptor one knockout (KO), AnxA1 KO, and formyl peptide receptor 2 (FPR2) KO mice were infected with

Indexed as

Annexin A1DengueAnimalsHumansInflammationMicePeptidesReceptors, Formyl PeptideReceptors, LipoxinAnnexin A1FPR2 protein, humanPeptidesReceptors, Formyl PeptideReceptors, LipoxinAc2-26 pro-resolving peptideAnnexin A1 pro-resolving proteindengue diseasedengue virusFPR2/ALX receptorhumanimmunologyinfectious diseaseinflammationinflammation resolutionmicrobiologymouseviruses

Identifiers

PMID35293862
PMCPMC8959599
OpenAlexW4226342464

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.