Evidence map›Paper›PMID 34943787›Full record

ArticleCells2021

SARS-CoV-2 Spike Protein and Its Receptor Binding Domain Promote a Proinflammatory Activation Profile on Human Dendritic Cells.

Dante Barreda, César Santiago, Juan R Rodríguez, José F Rodríguez, José M Casasnovas, Isabel Mérida, Antonia Ávila-Flores

Open access · goldAbstract read
In one paragraph

Article in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  10. Carbon dioxide and MAPK signalling: towards therapy for inflammation.Cell communication and signaling : CCS · 2023
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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

7 authors at 1 institution in 1 country.

Dante BarredaDepartment of Immunology and Oncology, Spanish National Centre for Biotechnology, 28049 Madrid, Spain.
César SantiagoDepartment of Macromolecular Structures, Spanish National Centre for Biotechnology, 28049 Madrid, Spain.
Juan R RodríguezDepartment of Molecular and Cell Biology, Spanish National Centre for Biotechnology, 28049 Madrid, Spain.
José F RodríguezDepartment of Molecular and Cell Biology, Spanish National Centre for Biotechnology, 28049 Madrid, Spain.
José M CasasnovasDepartment of Macromolecular Structures, Spanish National Centre for Biotechnology, 28049 Madrid, Spain.ORCID 0000-0002-2873-6410
Isabel MéridaDepartment of Immunology and Oncology, Spanish National Centre for Biotechnology, 28049 Madrid, Spain.ORCID 0000-0003-2762-6241
Antonia Ávila-FloresDepartment of Immunology and Oncology, Spanish National Centre for Biotechnology, 28049 Madrid, Spain.ORCID 0000-0001-6278-2472
Spanish National Centre for Cardiovascular Research · ES

Funding

Ministry of Economy, Industry and Competitiveness MINECO PID2019-108357RB-I00/10.13039/501100011033Spanish National Research Council CSIC-COVID19-032
6 · The paper itself

Abstract

Dendritic cells (DCs) are the most potent antigen-presenting cells, and their function is essential to configure adaptative immunity and avoid excessive inflammation. DCs are predicted to play a crucial role in the clinical evolution of the infection by the severe acute respiratory syndrome (SARS) coronavirus (CoV)-2. DCs interaction with the SARS-CoV-2 Spike protein, which mediates cell receptor binding and subsequent fusion of the viral particle with host cell, is a key step to induce effective immunity against this virus and in the S protein-based vaccination protocols. Here we evaluated human DCs in response to SARS-CoV-2 S protein, or to a fragment encompassing the receptor binding domain (RBD) challenge. Both proteins increased the expression of maturation markers, including MHC molecules and costimulatory receptors. DCs interaction with the SARS-CoV-2 S protein promotes activation of key signaling molecules involved in inflammation, including MAPK, AKT, STAT1, and NFκB, which correlates with the expression and secretion of distinctive proinflammatory cytokines. Differences in the expression of ACE2 along the differentiation of human monocytes to mature DCs and inter-donor were found. Our results show that SARS-CoV-2 S protein promotes inflammatory response and provides molecular links between individual variations and the degree of response against this virus.

Indexed as

Angiotensin-Converting Enzyme 2Cell Adhesion MoleculesCell DifferentiationCytokinesDC-Specific ICAM-3 Grabbing NonintegrinDendritic CellsExtracellular Signal-Regulated MAP KinasesHumansInflammationLectins, C-TypeProtein DomainsProto-Oncogene Proteins c-aktReceptors, Cell SurfaceReceptors, VirusSARS-CoV-2Signal TransductionACE2 protein, humanAngiotensin-Converting Enzyme 2Cell Adhesion MoleculesCytokinesDC-Specific ICAM-3 Grabbing NonintegrinExtracellular Signal-Regulated MAP KinasesLectins, C-TypeProto-Oncogene Proteins c-aktReceptors, Cell SurfaceReceptors, VirusSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2STAT Transcription FactorsACE-2COVID-19cytokinesinflammation

Identifiers

PMID34943787
PMCPMC8699033
OpenAlexW3215083396

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.