Another silenced subject concerning vaccines is the enzyme nagalase.
Nagalase is a protein excreted by cancer cells and viruses in the body. It prevents the naturally-occurring immune booster, Globulin component Macrophage Activating Factor (GcMAF), from being produced. High levels of nagalase have been found in patients with cancer, autism, diabetes, immune disorders, and viral and bacterial infections.
According to biotech company Firstimmune, a company that processes nagalase blood tests:
Increased activity of nagalase has been detected in the blood of patients with a wide variety of cancers, like cancer of the prostate, breast, colon, lung, oesophagus, stomach, liver, pancreas, kidney, bladder, testis, uterus and ovary, mesothelioma, melanoma, fibrosarcoma, glioblastoma, neuroblastoma, and various leukemias … Increased nagalase activity has not been detected in the blood of healthy humans.
Dr.
Jeff Bradstreet was one of many doctors investigating the role that viruses play in making nagalase.
Dr. Bradstreet states in a paper no longer available on his site, “Viruses make the nagalase enzyme as part of their attachment proteins. It serves to get the virus into the cell and also decreases the body’s immune reaction to the virus-thereby increasing the odds of viral survival.”
Nagalase In Vaccines
It’s not currently known whether or not nagalase is a contaminant in vaccines. Dr. Bradstreet was investigating whether its elevated concentration in children with autism and cancer is due to the antigenic viral envelope proteins used in vaccine production.
Dr. Bradstreet was treating his patients with autism with GcMAF. And, was conducting
clinical experiments to be published in medical journals. Tragically, Dr. Bradstreet was found bobbing in a river with a bullet wound to his chest. It was reported as a suicide. But, many doubt this after FDA agents and law enforcement raided his offices.
Three days earlier, he had received a warrant for all of his research about his use of GcMAF with his patients.
The role of nagalase in ASD and
the use of GcMAF for cancer treatment and ASD
continues to be studied by researchers.
Complete Human Genome DNA
“Vaccines must be grown in a ‘substrate’ which simply means that it takes living tissue to grow the microscopic vaccine ingredients. So where do they get the living tissue,” writes Ty Bolinger in his epic book
Monumental Myths of the Modern Medical Mafia and Mainstream Media.
In recent years it has come to light that vaccines are made using aborted fetal tissue. The claim means that vaccines merely contain
viruses that were grown on cells from aborted babies. However, Italian researchers have recently proven that this is an outright lie.
Scientists from an organization called
Corvelva tested the Measles-Mumps-Rubella-Varicella (MMRV) vaccine, Priorix Tetra manufactured by GlaxoSmithKline, and results showed that
the vaccine contained an entire human genome with the chromosomes of a male. And a bit of chicken DNA too, for good measure.
Even more alarming is that the genome is not one of a typical, healthy human being. They discovered several unknown variants. Some were located in the genes that are involved with cancer.
They state in their report:
What is also apparently anomalous, is the excess of the genome that shows changes in the number of copies … and structural variants … many of which involve genes. The potential contribution of the numerous variants (not present in the scientific literature and in public databases) to the phenotype of the cells used for the growth of vaccine viruses is not known.”
Shouldn’t We Be More Concerned?
Even before the Corvelva report, the correlation between the
introduction of fetal cell lines in vaccines and the spike in autism rates has been a concern for too few scientists. A former senior scientist at a pharmaceutical firm, Helen Ratajczak, has publicly expressed concerns over
the spike in autism following the introduction of human DNA to the MMR vaccine and the chickenpox vaccine.
Contrary to the “fetal cells are only used to grow viruses” soundbite, vaccines were discovered to contain unacceptably high levels of fetal DNA fragment contaminants. Dr. Teresa Deisher, a stem cell researcher, published a study in 2015 about
the relationship between DNA in vaccines and autism that concludes:
The human genome naturally contains regions that are susceptible to double-strand break formation and DNA insertional mutagenesis. The ‘Wakefield Scare’ created a natural experiment that may demonstrate a causal relationship between fetal cell-line manufactured vaccines and ASD prevalence.
And, perhaps, the most alarming revelation of Dr. Deisher’s research has been that
human DNA can integrate into the genome of a vaccinated person. In a study conducted at the Sound Choice Pharmaceuticals Institute, she discovered and concludes:
Not only damaged human cells, but also healthy human cells can take up foreign DNA spontaneously … Hence, residual human fetal DNA fragments in vaccine can be one of the causes of autism spectrum disorder in children through vaccination.
These dire concerns about the integration of human DNA are a long cry from the dismissive explanation that aborted fetal cells are only used to grow viruses for vaccines.
