Evidence map›Paper›PMID 36674654›Full record

ArticleInternational journal of molecular sciences2023

Zymosan Particle-Induced Hemodynamic, Cytokine and Blood Cell Changes in Pigs: An Innate Immune Stimulation Model with Relevance to Cytokine Storm Syndrome and Severe COVID-19.

Gábor Kökény, Tamás Bakos, Bálint András Barta, Georgina Viktória Nagy, Tamás Mészáros, Gergely T Kozma, András Szabó, János Szebeni, Béla Merkely, Tamás Radovits

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 4 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

10 authors at 1 institution in 2 countries.

Gábor KökényDepartment of Translational Medicine, Semmelweis University, 1089 Budapest, Hungary.ORCID 0000-0002-0345-6914
Tamás BakosNanomedicine Research and Education Center, Department of Translational Medicine, Semmelweis University, 1089 Budapest, Hungary.
Bálint András BartaHeart and Vascular Center, Semmelweis University, 1122 Budapest, Hungary.
Georgina Viktória NagyHeart and Vascular Center, Semmelweis University, 1122 Budapest, Hungary.
Tamás MészárosNanomedicine Research and Education Center, Department of Translational Medicine, Semmelweis University, 1089 Budapest, Hungary.
Gergely T KozmaNanomedicine Research and Education Center, Department of Translational Medicine, Semmelweis University, 1089 Budapest, Hungary.
András Szabó2nd Department of Pediatrics, Semmelweis University, 1085 Budapest, Hungary.
János SzebeniDepartment of Translational Medicine, Semmelweis University, 1089 Budapest, Hungary.
Béla MerkelyHeart and Vascular Center, Semmelweis University, 1122 Budapest, Hungary.
Tamás RadovitsHeart and Vascular Center, Semmelweis University, 1122 Budapest, Hungary.
Semmelweis University · HU

Funding

European comission 952520
6 · The paper itself

Abstract

Hemodynamic disturbance, a rise in neutrophil-to-lymphocyte ratio (NLR) and release of inflammatory cytokines into blood, is a bad prognostic indicator in severe COVID-19 and other diseases involving cytokine storm syndrome (CSS). The purpose of this study was to explore if zymosan, a known stimulator of the innate immune system, could reproduce these changes in pigs. Pigs were instrumented for hemodynamic analysis and, after i.v. administration of zymosan, serial blood samples were taken to measure blood cell changes, cytokine gene transcription in PBMC and blood levels of inflammatory cytokines, using qPCR and ELISA. Zymosan bolus (0.1 mg/kg) elicited transient hemodynamic disturbance within minutes without detectable cytokine or blood cell changes. In contrast, infusion of 1 mg/kg zymosan triggered maximal pulmonary hypertension with tachycardia, lasting for 30 min. This was followed by a transient granulopenia and then, up to 6 h, major granulocytosis, resulting in a 3-4-fold increase in NLR. These changes were paralleled by massive transcription and/or rise in IL-6, TNF-alpha, CCL-2, CXCL-10, and IL-1RA in blood. There was significant correlation between lymphopenia and IL-6 gene expression. We conclude that the presented model may enable mechanistic studies on late-stage COVID-19 and CSS, as well as streamlined drug testing against these conditions.

Indexed as

COVID-19CytokinesAnimalsCytokine Release SyndromeImmunity, InnateInterleukin-6Leukocytes, MononuclearSwineZymosanCytokinesInterleukin-6Zymosananimal modelschemokinescytokine stormgranulocytesIL-1betaIL-6inflammatory cytokineslymphocytespigspulmonary hypertensionsystemic inflammationwhite blood cells

Identifiers

PMID36674654
PMCPMC9863690
OpenAlexW4313815478

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.