Evidence map›Paper›PMID 33362782›Full record

ArticleFrontiers in immunology2020

NF-κB Pathway as a Potential Target for Treatment of Critical Stage COVID-19 Patients.

Ralf Kircheis, Emanuel Haasbach, Daniel Lueftenegger, Willm T Heyken, Matthias Ocker, Oliver Planz

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 140 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
140citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 4% 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

140 citing papers in PubMed, 1 synthesis or guideline pooled it, 209 citations in OpenAlex.

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

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

6 authors at 2 institutions in 1 country.

Ralf KircheisVirologik GmbH, Erlangen, Germany.
Emanuel HaasbachInstitute of Cell Biology and Immunology, Eberhard Karls University Tuebingen, Tuebingen, Germany.
Daniel LuefteneggerVirologik GmbH, Erlangen, Germany.
Willm T HeykenVirologik GmbH, Erlangen, Germany.
Matthias OckerInstitute for Surgical Research, Philipps University of Marburg, Marburg, Germany.
Oliver PlanzInstitute of Cell Biology and Immunology, Eberhard Karls University Tuebingen, Tuebingen, Germany.
University of Tübingen · DEPhilipps University of Marburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients infected with SARS-CoV-2 show a wide spectrum of clinical manifestations ranging from mild febrile illness and cough up to acute respiratory distress syndrome, multiple organ failure, and death. Data from patients with severe clinical manifestations compared to patients with mild symptoms indicate that highly dysregulated exuberant inflammatory responses correlate with severity of disease and lethality. Epithelial-immune cell interactions and elevated cytokine and chemokine levels, i.e. cytokine storm, seem to play a central role in severity and lethality in COVID-19. The present perspective places a central cellular pro-inflammatory signal pathway, NF-κB, in the context of recently published data for COVID-19 and provides a hypothesis for a therapeutic approach aiming at the simultaneous inhibition of whole cascades of pro-inflammatory cytokines and chemokines. The simultaneous inhibition of multiple cytokines/chemokines is expected to have much higher therapeutic potential as compared to single target approaches to prevent cascade (i.e. redundant, triggering, amplifying, and synergistic) effects of multiple induced cytokines and chemokines in critical stage COVID-19 patients.

Indexed as

COVID-19 Drug TreatmentAnimalsCOVID-19Cytokine Release SyndromeCytokinesDisease Models, AnimalHumansInfluenza A Virus, H1N1 SubtypeInfluenza A Virus, H5N1 SubtypeMiceMice, Inbred BALB CNF-kappa BOrthomyxoviridae InfectionsProteasome InhibitorsSARS-CoV-2CytokinesNF-kappa BProteasome InhibitorschemokinesCOVID-19cytokinescytokine stormNF-KappaBNSAIDproteasome inhibitorSARS-CoV-2 (2019-nCoV)

Identifiers

PMID33362782
PMCPMC7759159
OpenAlexW3110713218

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.