In December 2020, the first vaccines for corona virus disease were granted an EUA – Emergency Use Authorization – by the Food and Drug Administration (FDA) and recommended by the Advisory Committee on Immunization Practices (ACIP). Vaccine administration began immediately. Were you first in line? I hope you were not, and I hope no one you care about ran to get this injection either.

This is not “just another vaccine”  and this is not “just like getting a flu shot.” The ingredients are experimental and the mRNA is coded to produce a protein that CAN modify your DNA.

AstraZeneca ChAdOx1 nCoV-19 is a recombinant adenovirus vaccine candidate against SARS-CoV-2. 

clinical studies, done in collaboration with the University of Oxford, were widely publicized as the first and most promising vaccine. However, in May 2020, it was reported that all the vaccinated monkeys treated with the Oxford vaccine became infected when challenged. Then, why did the company press forward with the vaccine candidate? Because even though the vaccine did not protect the animals from infection, it did moderate the disease. Watch for this type of logic as the 80+ COVID vaccines try to make their way into the multi-trillion-dollar vaccine market.

Vaccine-induced Spike Antibodies: Havoc on the Lungs

When the corona virus vaccine is injected, the mRNA contains “instructions” for building the spike protein that has been identified on the surface of the SARS-CoV2 virus. The cell’s reverse transcriptase enzymes are called into action, leading to the mass production of the spike (S) protein, the protein thought to play a vital role in its infectivity.

However, is this a good thing? What the researchers discovered was startling.

Sixteen macaque monkeys were given two injections; half of the animals received a modified vaccinia virus with an inserted spike protein (ADS-MVA) or a control vaccine made with a modified vaccinia virus without the spike protein antigen (ADC-MVA). Three healthy, non-vaccinated monkeys were included as additional controls.

The animals were sacrificed between weeks 9 and 21, after receiving the second injection; the vaccine containing the spike protein induced very high antibody responses to the spike protein (anti-S-IgG). Although the antibodies had reduced the viral load in the upper respiratory tract, they caused a serious, antibody-enhanced injury in the lungs. In fact, there was a direct and positive correlation between the level of antibody in serum and the degree of lung injury. The tissues had evidence of diffuse alveolar damage (DAD), with various degrees of exudate (pus-like fluid) and hemorrhage (bleeding).

Even more, the lungs were filled with large quantities of macrophages (pus) that had been weakened and inactivated.

Macrophages are a type of white blood cell that engulf, digest and eliminate microbes and foreign proteins through a process called phagocytosis. There are two primary types of macrophages. The M1 cells kill pathogens by secreting pro-inflammatory mediators and the M2 cells, which have an anti-inflammatory function and regulate wound healing. Antibodies formed against the SARS-CoV spike protein binds to the surface of M2 macrophages and weaken their function, allowing the M1 macrophages to release unchecked quantities cytokines. Instead of healing and repairing the infected lung tissues, the anti-S-IgG antibodies stifle the M2 cells and promote M1-caused inflammation. The results are a disaster.

The above study was very recent (2019) but is it one of MANY dating back to 2002 documenting how damaging the COVID vaccine(s) are going to be once a person is vaccinated and then is re-exposed to circulating corona viruses.

The ChAdOx1 vector virus is derived from chimpanzee adenovirus Y25 with two regions deleted  E1 and E3 genes. In addition, parts of the E4 region of the Y25 virus have been replaced with the equivalent E4 regions from HuAd5 to facilitate growth in HEK293 cells.

Adenovirus based vectors typically have two regions of the virus genome removed, known as E1 and E3. The E1 region contains early genes required to trigger a transcription cascade enabling viral replication; E1 deleted vectors therefore need to be grown in E1 trans-complementing cell lines such as HEK293 cells.

Adenovirus based vaccines are grown in HEK293 cells (or equivalents) to very high titres, purified and then administered to individuals.

A titer is a laboratory test that measures the presence and amount of antibodies in blood. A titer may be used to prove immunity to disease. A blood sample is taken and tested. If the test is positive (above a particular known value) the individual has immunity.

HEK293 cells are Human Embryonic Kidney cells, originally isolated and grown by Dutch biologist Alex Van der Eb in the early 1970s. They were transfected with sheared adenovirus 5 (Ad5) DNA by Frank Graham, a postdoc in Van der Eb’s lab. It was his 293rd experiment, which is why they got the tag HEK293

Usually, the transgene to be expressed is inserted into the virus genome in place of the E1 region.

 A transgene is a gene that has been transferred naturally, or by any of a number of genetic engineering techniques from one organism to another. The introduction of a transgene, in a process known as transgenesis, has the potential to change the phenotype of an organism.

Transgenesis is the process of introducing a gene (referred to as a transgene) from one organism into the genome of another organism. The aim is that the resulting transgenic organism will express the gene and exhibit some new property or characteristic.


the set of observable characteristics of an individual resulting from the interaction of its genotype with the environment.


the genetic constitution of an individual organism.

The E3 region is comprised of genes encoding proteins that primarily act to subvert the immune response to adenovirus infection and are thus not needed for replication in cell culture and potentially undesirable from a vaccine platform perspective.

What is Recombinant or Purified Protein Vaccines?

Recombinant or purified protein vaccines consist of protein antigens that have either been produced in a heterologous expression system (e.g., bacteria or yeast) or purified from large amounts of the pathogenic organism. The vaccinated person produces antibodies to the protein antigen, thus protecting him/her from disease.

Medical Definition of pathogenic: causing or capable of causing disease pathogenic microorganisms.

Thus as it is grown in fetal tissue it is purified of any disease causing material. Not the fetal tissue itself!

Adenoviruses are non-enveloped viruses containing a linear double stranded DNA genome of approximately 36 kbp that efficiently deliver their DNA genome to the nuclei of host cells for viral genome replication. 

The virus will attach to a host cell, enter and deliver the recombinant genome to the nucleus where the desired gene of interest is expressed. 

Thus it alters your DNA!


Typically, the lack of E1 encoded proteins should ensure that there is no productive viral replication. However, it is noteworthy that removal of the E1 and E3 regions still leaves a number of other viral genes and promoters, including the E2 and E4 regions. Moreover, background expression of at least some of these adenovirus genes has been previously identified in studies with human adenovirus based vectors. Expression of these viral vector genes may lead to the production of adenoviral antigens which in turn would bring the cell to the attention of the adaptive immune response.  In principle this could lead to vaccine vector infected cells being eliminated before an adaptive response to the vaccine target is raised; especially if repeat re-administration is desired. This has prompted the development of adenovirus vectors based on strains of adenovirus for which there is little or no pre-existing immunity in the general human population15.

Adaptive response and oxidative stress.

The ability of a cell, tissue, or organism to better resist stress damage by prior exposure to a lesser amount of stress is known as adaptive response. It is observed in all organisms in response to a number of different cytotoxic agents.

Thus the vaccine is causing new strains of the virus!

So they are saying the vaccine could eliminate cells before they build immunity to the virus

The engineered viruses, called adenoviral vectors, are designed to shuttle a gene from SARS-CoV-2, the novel coronavirus that causes COVID-19, into our bodies where our cells will read it and make coronavirus spike proteins.

Adenoviruses is not a nationally notifiable disease in the United States, meaning clinicians are not required to test for or report cases to health departments or CDC. Therefore, many outbreaks of adenovirus likely go either undetected or unreported.

Bottom line- The vaccine is grown in fetal tissue and thus it contains fetal tissue. Also it will alter your DNA! And finally because of how it was created it can kill cells before they can develop immunity, and create now strains of the virus that you could pass onto others!

Remember that both vaccines are completely protected from all liability by the 2005 PREP Act. So, if the nurse gives you the wrong shot, and you have a serious reaction, even death, there will be no repercussions for the nurse and no compensation for you.

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