Devastating study by Poloni et al. on spike protein from mRNA technology mRNA vaccines 'causing' MYOCARDITIS, heart damage yet study is focused on COVID virus! Why? How could I make this extrapolation

Study reports 'traces' of COVID virus in heart cells (endothelium/myocardium); myocarditis is caused by mRNA vaccine; yet the authors of this study has taken virus off the table as implicated in heart

This Poloni et al. study did well to rule out Myocarditis originating from COVID (SARS-CoV-2) Infection and likely with near certainty, from mRNA vaccine. I explain below.

So if someone took mRNA vaccine and likely they did, and there is myocarditis, pericarditis, heart inflammation etc., then it is likely, more assuredly, that it is due to the mRNA vaccine. This study by OMISSION, is taking us closest to showing that the vaccine is causing the heart damage when one presents with myocarditis in this era of COVID mRNA vaccines.

So I am arguing that these results by Poloni et al. point to vaccine as the likely culprit in myocarditis. Check for vaccine status always. The mRNA technology vaccine is so very devastating that even if you get a heart transplant due to heart damage post mRNA vaccine, we are now having reports that the new heart is and can become riddled with myocarditis AGAIN. The cellular machinary is highjacked likely lifelong and produces spike protein forever. You have damaged yourself forever with these mRNA technology gene mRNA vaccines. Immune dysregulation, subversion, actual heart damage, strokes, bleeding, aneurysms, clotting etc.

https://pubmed.ncbi.nlm.nih.gov/36231087/

‘Lungs, kidneys, hearts, and brains from nine COVID-19 autopsies were compared by using antibodies against SARS-CoV-2, macrophages-microglia, T-lymphocytes, B-lymphocytes, and activated platelets.

Alzheimer's Disease pathology was also assessed. PCR techniques were used to verify the presence of viral RNA.

COVID-19 cases had a short clinical course (0-32 days) and their mean age was 77.4 y/o.

Hypoxic changes and inflammatory infiltrates were present across all tissues. The lymphocytic component in the lungs and kidneys was predominant over that of other tissues (p < 0.001), with a significantly greater presence of T-lymphocytes in the lungs (p = 0.020), which showed the greatest presence of viral antigens.

The heart showed scant SARS-CoV-2 (virus insert) traces in the endothelium-endocardium, foci of activated macrophages, and rare lymphocytes.

The brain showed scarce SARS-CoV-2 traces, prominent microglial activation, and rare lymphocytes.’