Evidence map›Paper›PMID 28351919›Full record

ArticlemBio2017

Contribution of the Purinergic Receptor P2X7 to Development of Lung Immunopathology during Influenza Virus Infection.

Victor H Leyva-Grado, Megan E Ermler, Michael Schotsaert, Ma G Gonzalez, Virginia Gillespie, Jean K Lim, Adolfo García-Sastre

Open access · goldAbstract read
In one paragraph

Article in mBio, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

30 citing papers in PubMed, 48 citations in OpenAlex.

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  18. P2 Purinergic Signaling in the Distal Lung in Health and Disease.International journal of molecular sciences · 2020
    Review
  19. Review
  20. Low level laser therapy as a modality to attenuate cytokine storm at multiple levels, enhance recovery, and reduce the use of ventilators in COVID-19.Canadian journal of respiratory therapy : CJRT = Revue canadienne de la therapie respiratoire : RCTR · 2020
    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

7 authors at 1 institution in 1 country.

Victor H Leyva-GradoDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, New York, USA victor.leyva-grado@mssm.edu.ORCID 0000-0002-9211-6160
Megan E ErmlerDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Michael SchotsaertDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Ma G GonzalezCenter for Comparative Medicine and Surgery, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Virginia GillespieCenter for Comparative Medicine and Surgery, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Jean K LimDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Adolfo García-SastreDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Icahn School of Medicine at Mount Sinai · US

Funding

NIAID NIH HHS HHSN272201400008C
6 · The paper itself

Abstract

An exacerbated immune response is one of the main causes of influenza-induced lung damage during infection. The molecular mechanisms regulating the fate of the initial immune response to infection, either as a protective response or as detrimental immunopathology, are not well understood. The purinergic receptor P2X7 is an ionotropic nucleotide-gated ion channel receptor expressed on immune cells that has been implicated in induction and maintenance of excessive inflammation. Here, we analyze the role of this receptor in a mouse model of influenza virus infection using a receptor knockout (KO) mouse strain. Our results demonstrate that the absence of the P2X7 receptor results in a better outcome to influenza virus infection characterized by reduced weight loss and increased survival upon experimental influenza challenge compared to wild-type mice. This effect was not virus strain specific. Overall lung pathology and apoptosis were reduced in virus-infected KO mice. Production of proinflammatory cytokines and chemokines such as interleukin-10 (IL-10), gamma interferon (IFN-γ), and CC chemokine ligand 2 (CCL2) was also reduced in the lungs of the infected KO mice. Infiltration of neutrophils and depletion of CD11b

Indexed as

Host-Pathogen InteractionsAnimalsBody WeightCytokinesDisease Models, AnimalLungMacrophagesMiceMice, KnockoutNeutrophilsOrthomyxoviridaeOrthomyxoviridae InfectionsReceptors, Purinergic P2X7Survival AnalysisCytokinesReceptors, Purinergic P2X7cytokinesextracellular ATPimmunopathologyinfluenzapurinergic receptor

Identifiers

PMID28351919
PMCPMC5371412
OpenAlexW2603350173

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.