In new a study published last week in the journal Vaccines, Russia’s Vector Institute detailed how it engineered a lab-built H5 influenza spike protein—chemically optimized for durability and mass expression—under the banner of needle-free jet injection vaccine development.
The study, titled “Immunogenic and Protective Properties of mRNA Vaccine Encoding Hemagglutinin of Avian Influenza A/H5N8 Virus, Delivered by Lipid Nanoparticles and Needle-Free Jet Injection,” confirms yet another link in the chain of international bird flu pandemic countermeasure orchestration.
Lab-Built Hemagglutinin (HA)
The authors openly admit that they deliberately cut away the natural anchor of the bird flu spike and rebuilt it to be secreted outside the cell.
“In brief, the transmembrane and cytoplasmic domains were excised from the native HA sequence. For the purpose of secretion from cells, the signal peptide from the native sequence was retained,” the researchers write.
And further, they took the bird flu spike gene, inserted it into a lab plasmid, and added human RNA control elements plus a long poly(A) tail to boost expression.
“The HA gene, designed based on the native HA gene of the influenza virus A/turkey/Stavropol/320-01/2020 (H5N8) … was cloned into the pVAX-Cas1CC expression cassette … The cassette also contains the human α-globin 5′- and 3′-untranslated regions, as well as a 100-nucleotide poly (A) tail.”
They even confirm the same chemical alteration used in the Pfizer and Moderna COVID-19 shots:
“mRNA synthesis was performed … with uridine replaced by N1-methylpseudouridine.”
Pseudouridine—the synthetic mRNA ingredient swapped in for natural uridine—has now been shown to cause ribosomal “frameshifting” that makes the body attack its own proteins in roughly one-third of recipients, and in other studies has been linked to stimulating cancer growth and metastasis.
Hellbound and Down 