Evidence map›Paper›PMID 32353634›Full record

ReviewClinical immunology (Orlando, Fla.)2020

COVID-19: Immunology and treatment options.

Susanna Felsenstein, Jenny A Herbert, Paul S McNamara, Christian M Hedrich

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Clinical immunology (Orlando, Fla.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04531319 (Evaluation of Immune Cell Subgroups in Covid 19 Patients), which is not on this map. Cited by 340 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
340citing papers in PubMed, 1 pooled it
16.0field-weighted citation impact, top 1% 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.

NCT04531319 completednot on this map

Evaluation of Immune Cell Subgroups in Covid 19 Patients

TypeobservationalSponsorIstanbul Training and Research HospitalRan2020 to 2020Enrolled50ConditionsCovid19ArmsFlow cytometric analysis
3 · Its place in the literature

Who cites it

340 citing papers in PubMed, 1 synthesis or guideline pooled it, 685 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  20. Evaluation of the relationship betweenAsian biomedicine : research, reviews and news · 2024
    Article

280 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Susanna FelsensteinDepartment of Infectious Diseases and Immunology, Alder Hey Children's NHS Foundation Trust Hospital, Liverpool, UK.
Jenny A HerbertDepartment of Women's & Children's Health, Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
Paul S McNamaraDepartment of Women's & Children's Health, Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
Christian M HedrichDepartment of Women's & Children's Health, Institute of Translational Medicine, University of Liverpool, Liverpool, UK; Department of Paediatric Rheumatology, Alder Hey Children's NHS Foundation Trust Hospital, Liverpool, UK. Electronic address: christian.hedrich@liverpool.ac.uk.
University of Liverpool · GBAlder Hey Children's NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The novel coronavirus SARS-CoV2 causes COVID-19, a pandemic threatening millions. As protective immunity does not exist in humans and the virus is capable of escaping innate immune responses, it can proliferate, unhindered, in primarily infected tissues. Subsequent cell death results in the release of virus particles and intracellular components to the extracellular space, which result in immune cell recruitment, the generation of immune complexes and associated damage. Infection of monocytes/macrophages and/or recruitment of uninfected immune cells can result in massive inflammatory responses later in the disease. Uncontrolled production of pro-inflammatory mediators contributes to ARDS and cytokine storm syndrome. Antiviral agents and immune modulating treatments are currently being trialled. Understanding immune evasion strategies of SARS-CoV2 and the resulting delayed massive immune response will result in the identification of biomarkers that predict outcomes as well as phenotype and disease stage specific treatments that will likely include both antiviral and immune modulating agents.

Indexed as

PandemicsAngiotensin-Converting Enzyme 2Antiviral AgentsAzithromycinBetacoronavirusCoronavirus InfectionsCOVID-19CytokinesDisease ManagementGene Expression RegulationHumansHydroxychloroquineImmune EvasionImmunologic FactorsPeptidyl-Dipeptidase APneumonia, ViralACE2 protein, humanAngiotensin-Converting Enzyme 2Antiviral AgentsAzithromycinCytokinesHydroxychloroquineImmunologic FactorsPeptidyl-Dipeptidase ASpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Toll-Like ReceptorsTumor Necrosis Factor Receptor-Associated Peptides and Proteins

Identifiers

PMID32353634
PMCPMC7185015
OpenAlexW3018494531

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.