I came across this tweet in my feed:
The claim is that a group of scientists from Corvelva tested a sample of MMRV and determined that it contained human DNA.
The human reference genome was found to be matched by 99.76% reads from vaccine DNA, that means nearly in all its entirety. The human fetal DNA presented in this vaccine is a single entire genome, that means the vaccine contains genomic DNA with all the chromosomes of a male individual (in fact MRC-5 originates from a male fetus).
For context, from the full report:
Below is an extract of the document kindly provided by Dr. Theresa Deisher:
● Recently, duplications and de novo deletions have been recognized in up to 10% of simplex autism spectrum disorders, corroborating environmental triggers on the genetics of autism spectrum disorders.
● The rubella portion of the MMR vaccine contains human derived fetal DNA contaminants of about 175 ngs, more than 10x over the recommended WHO threshold of 10 ng per vaccine dose.
● No other drug on the market would receive FDA approval without thorough toxicity profiling (FDA follows international ICH guidelines) -> this was never conducted by the pharmaceutical industry for the DNA contamination in the MMR vaccine.
● Vaccines produced with human fetal cell lines contain cell debris and contaminating residual human DNA, which cannot be fully eliminated during the downstream purification process of the virus. Moreover, DNA is not only characterized by its sequence (ATCG), but also by its epigenetic modification (e.g. DNA methylation pattern etc.). This decoration is highly species specific, which is why non-human DNA will be eliminated, while this is not necessarily the case with fetal human DNA.
Injecting our children with human fetal DNA contaminants bears the risk of causing two well-established pathologies:
Insertional mutagenesis: fetal human DNA incorporates into the child’s DNA causing mutations. Gene therapy using small fragment homologous recombination has demonstrated that as low as 1.9 ng/ml of DNA fragments results in insertion into the genome of stem cells in 100% of mice injected.
The levels of human fetal DNA fragments in our children after vaccination with MMR, Varivax (chickenpox) or Hepatitis A containing vaccines reach levels beyond 1.9 ng/ml.
Autoimmune disease: fetal human DNA triggers a child’s immune system to attack his/her own body.
The results that we obtained in this first part of sequencing of the complete MRC-5 genome present in the vaccine (the second part is the sequencing of the entire genome of the MRC-5 cell line used to cultivate the vaccine virus and the comparative analysis with the Fetal DNA vaccine) considerably strengthen the experimental observations of Dr. Deisher and above all the fact that the contaminating fetal DNA present in all the samples analyzed in variable quantities (therefore not controlled) is up to 300 times higher than the limit imposed by the EMA for the carcinogenic DNA (10 ng / dose, corresponding to the DNA contained in about 1000 tumor cells, obtained on the basis of a statistical calculation, while the precautionary limit is 100 pg / dose) limit that must necessarily be applied also to the fetal DNA that inevitably contaminates the Priorix ® tetra.
As a consequence, this vaccine should be considered defective and potentially dangerous for human health, in particular of the pediatric population, who is much more vulnerable to genetic and autoimmune damage due to immaturity in their repair systems.