Evidence mapPaperPMID 37112659Full record

ReviewVaccines2023

COVID-19 mRNA Vaccines: The Molecular Basis of Some Adverse Events.

Girolamo Giannotta, Antonio Murrone, Nicola Giannotta

Abstract readReview
In one paragraph

Review in Vaccines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
field-weighted citation impact
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

32 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  9. Observational
  10. Preharvest Control ofMicroorganisms · 2025
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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

3 authors.

Girolamo GiannottaAzienda Sanitaria Provinciale Vibo Valentia, 89900 Vibo Valentia, Italy.ORCID 0000-0001-9766-3326
Antonio MurroneOncologia Territoriale, Hospice Cure Palliative ASUFC, 33030 Udine, Italy.
Nicola GiannottaMedical and Surgery Sciences, Faculty of Medicine, Magna Græcia University, 88100 Catanzaro, Italy.ORCID 0000-0003-1701-7696

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Each injection of any known vaccine results in a strong expression of pro-inflammatory cytokines. This is the result of the innate immune system activation, without which no adaptive response to the injection of vaccines is possible. Unfortunately, the degree of inflammation produced by COVID-19 mRNA vaccines is variable, probably depending on genetic background and previous immune experiences, which through epigenetic modifications could have made the innate immune system of each individual tolerant or reactive to subsequent immune stimulations.We hypothesize that we can move from a limited pro-inflammatory condition to conditions of increasing expression of pro-inflammatory cytokines that can culminate in multisystem hyperinflammatory syndromes following COVID-19 mRNA vaccines (MIS-V). We have graphically represented this idea in a hypothetical inflammatory pyramid (IP) and we have correlated the time factor to the degree of inflammation produced after the injection of vaccines. Furthermore, we have placed the clinical manifestations within this hypothetical IP, correlating them to the degree of inflammation produced. Surprisingly, excluding the possible presence of an early MIS-V, the time factor and the complexity of clinical manifestations are correlated to the increasing degree of inflammation: symptoms, heart disease and syndromes (MIS-V).

Indexed as

arrhythmias and COVID-19 mRNA vaccinesCOVID-19 mRNA vaccine adverse eventsCOVID-19 mRNA vaccinesMIS-AMIS-CMIS-Vmultisystem inflammatory syndrome and COVID-19 mRNA vaccinesmyocarditismyo-pericarditis and COVID-19 mRNA vaccinespathogenesis of myocarditis following COVID-19 mRNA vaccines

Identifiers

PMID37112659
PMCPMC10145134

What Socratic 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 Socratic graph.