In the case of the COVID-19 vaccines, the media and the medical establishment tried getting around this by arguing that since the vaccines did not change the recipient’s DNA, that meant that they weren’t gene therapy. The introduction of foreign nucleic acids into the body to generate foreign proteins is, by definition, gene therapy, regardless of whether or not the subject’s own genes are changed by it. DNA and RNA are genetic material, and if the immune system catches a cell producing non-human proteins, some seriously bad things will happen to that cell.
… Unlike a virus, which only binds to specific host factors expressed by specific cell lines and is endocytosed in those specific cells, cationic lipids, like the LNPs used in mRNA vaccines, are capable of transfecting basically any type of cell with instructions to make proteins. LNPs were investigated for many years as a means of delivering Alzheimer’s drugs to the brain, because they readily bypass the blood-brain barrier.
When the thing being delivered is a toxin, like SARS-CoV-2 Spike, however, there are serious consequences.
… ADEPT is a DARPA program that began in 2012. The acronym stands for Autonomous Diagnostics to Enable Prevention and Therapeutics. PROTECT is a sub-program of ADEPT, and it stands for Prophylactic Options to Environmental and Contagious Threats.
… Apparently, the goal of ADEPT: PROTECT was to come up with nucleic acid delivery systems that encoded monoclonal antibodies (or mAbs) against specific pathogens that may be used in biowarfare, such as Influenza, Smallpox, SARS, Chikungunya, Rabies, Anthrax bacteria, and even Ricin, nerve agents, and prions.