The various COVID vaccines being rushed into existence do not operate as traditional biologics (vaccines) and are being falsely represented and regulated as such. Standard vaccines introduce attenuated (weakened) forms of a target virus, in conjunction with inflammatory adjuvant and other chemicals. These new mRNA, adenovirus-vectored, and DNA vaccines utilize the “software” of the virus, forcing the body to make copies of it.
Professor Jonathan Gershoni from Israel’s Tel Aviv University explains that three covid vaccines on the market are actually DNA vaccines. Inoculations manufactured by Sputnik V, AstraZeneca and Johnson & Johnson contain DNA (not just RNA) that is inserted into the nucleus of human cells to ultimately translate and replicate lab engineered spike proteins.
India is getting a new type of DNA vaccine made by Zydus Cadila; it will be called ZyCoV-D. This vaccine contains less DNA than the other DNA vaccines and that DNA is not concealed by a viral vector (adenovirus). For these vaccines, the 1,200 amino acid sequence of the coronavirus spike protein is contained in a plasmid, and it is administered intra-dermally in a three dose, three-month protocol using a high-pressure stream of liquid containing the DNA.
The adenovirus-vectored covid vaccines all contain DNA from the engineered spike protein. These vaccines stealthily deliver DNA from the bioweapon, concealing it in an adenovirus shell. Once the spike protein DNA bypasses the innate immune system, its genetic instructions are transcribed into the human cells, mass producing lab engineered spike proteins.
The pharmaceutical media and the fact checkers continue to lie about the experimental, gene-altering science behind new COVID vaccines. In unison, they claim that the vaccines do not alter human DNA or change genetic expression. However, these vaccines are genetic experiments designed to keep humans dependent on vaccine updates; the inoculations were designed to breach the innate immune system for the purpose of altering how cells read the body’s own genetic code.
The adenovirus-vectored vaccines carry the spike protein DNA into the cell by using the adenovirus to subvert the innate immune response. The mRNA vaccines use lipid nano-particles to conceal the instructions and slip them into the ribosomes of the cell. In the initial process of subverting the immune system, these vaccines do not beckon a strong enough T cell response to elicit adequate T helper 1, T helper 2, and memory B cells. Because the innate immune system is not exposed to the whole virus, including the envelope and the nucleocapsid, the immune system SUFFERS. This incomplete and subverted immune response primes the body for severe disease upon subsequent re-infection.
With this new vaccine technology, the messenger RNA or the DNA of a foreign, lab engineered spike protein is inserted into the body to overwrite the natural protein synthesis of the affected cells. Once this natural transcription process is re-engineered by the vaccines, there’s no guarantee that the cells will stop using this foreign code. There are no studies mapping where the spike proteins travel to in the body, how long they might last, or if their replication alters protein synthesis indefinitely and becomes a part of human cells or human DNA.
Because DNA is unable to transcribe by itself, the DNA vaccines must insert the foreign DNA into the nucleus of the human cell. This allows messenger RNA to make a disposable copy of the DNA, preparing instructions for protein synthesis in the ribosome. The RNA has the ability to interact with the ribosomes of the cell, and is responsible for encoding the type of protein the cell is instructed to manufacture.
As predominant mutations of the spike protein are discovered in the wild, vaccine makers can study that DNA and retool the DNA and mRNA in their vaccines, to replicate new sequences of spike protein in humans each year.