Category: knockdown

Posted on by Ariyana Love

By Dr. Ariyana Love (ND)

Dr. Li-Meng Yan claims to be a “whistleblower” who’s against the CCP. She worked as a virologist in a Hong Kong lab with her husband who is also a virologist.

On February 15th, Dr. Yan supposedly blew the whistle saying she was given inside information that the CCP was planning to disseminate biological weapons at the winter Olympics in Beijing by releasing a “virus” that will induce hemorrhagic fever. She seemed to be setting the stage for us to believe that such an attack would lead to a Marburg outbreak.

While the CCP could easily have unleashed a bioweapon on people attending the winter Olympics, would that actually be able to induce the next staged plandemic, worldwide? I think not.

More than likely this is a ruse and a diversion from the fact that Marburg has already been injected into the world’s population through the Johnson & Johnson “vaccine”. The J&J patent specifically says that it contains Ebola and Marburg, a mRNA bioweapon that induces hemorrhagic fever. In fact, Frontline doctors are already seeing Hemorrhagic Fever showing up in the vaccinated population.

Dr. Yan went on to say that the CCP has an “antidote” calledDarzalex (daratumumab). Darzalex is an experimental drug using monoclonal antibodies. Is it a coincidence that J&J also owns the Darzalex patent and is now conveniently offering the supposed “antidote”? Problem, reaction, solution?

PATENT REVIEW

The Darzalex (daratumumab) patent was filed in 2015 for the treatment of Multiple Myeloma (MM) which is cancer. It was approved in the US by the FDA, for the treatment of patients with multiple myeloma in 2018, despite that a lawsuit was filed against Janssen Biotech Inc. in 2016, for patent infringement.

It is in fact, illegal to use monoclonal antibodies for any other treatment than myeloma, like “covid” symptoms or vaccine injury, for example. Despite that, MM patients have a 4-7 year life expectancy and therefore this is an end of life treatment.

In November 2020, Another monoclonal antibody combination of Casirivimab and Imdevimab made by Regeneron,was approved for use by the FDA for the treatment of Covid-19. It was approved under an Emergency Use Authorization because it’s an entirely experimental drug which uses “laboratory-made proteins”. It has never been tested on Humans and by their own admission, has never been proven safe and effective.

Regeneron warns that you can expect a “worsening of symptoms after treatment that may result in hospitalization”. I suppose that how you know it’s working. Also, the side effects of monoclonal antibodies “may be life-threatening”.

Grant funding for monoclonal antibodies came from the NIH, DAPRA, the Bill and Melinda Gates Foundation, the Musk Foundation, Janssen Pharmaceuticals, Gilead Sciences Inc., Pfizer Inc, and the University of North Carolina Chapel Hill, to name a few. This so called “treatment” is also part of Operation Warp Speed.

In a 2021 video, Bill Gates was promoting monoclonal antibodies as the next singular “treatment” for Covid-19.

Monoclonal antibodies reportedly “block the SARS-COV2 spike protein RBD from binding to the human ACE2 receptor”. However, studies reveal that monoclonal antibodies lessen the likelihood of SAR-CoV-2 resistance by 100 fold.

The Darzalex (daratumubad) patent includes a GenBank Accession Nos. NM_001775 which is a clone Lentiviral vector (nucleic acid sequence) and a NP_001766 is a cDNA (complementary DNA). I have documented previously that the Lentiviral vector contain the SARS, MERS, HIV 1-3, and SRV-1 bioweapons and that “cDNA” is used for cloning and patent eligibility.

The monoclonal antibody patent #10787501 uses “RNA and DNA vectors”, or polynucleotides. The patent also reveals this is a “vaccine“. This is experimental “Gene Therapy” using chimeric mRNA technology.

The patent mentions that “some embodiments” contains chloroquine or hydroxychloroquine while other embodiments contain only the immune suppressing agents. For example, HCDR1R is used in the “treatment” of Lupus which is a “down-regulation” of genes. HCDR2 gene clusters are also used in monoclonal antibodies for DNA binding and gene knockdowns using CRISPR.

Thermo Fischer provides monoclonal antibodies using CRISPR, for gene editing and knockdown. Labome is a key supplier of the “antibodies” used in monoclonal antibodies. Labome’s website admits it’s product is used for Human “cloning“.

The patent also says it contains LCDR2 which has Anthony Fauci’s HIV-1 patented bioweapon vector. It should be noted that the LCDR3 mentioned in the patent is the DNA of a humanized, chimeric mouse/human hybrid species. That’s definitely experimental and unsafe to inject in Humans. Any honest doctor will tell you this.

The patent says “In some embodiments, the coronavirus is selected from the group consisting of SARS-CoV-2, SARS-CoV, and MERS-CoV”. This literally means that monoclonal antibodies contain SARS and MERS. We know that SARS and MERS are bioweapons and that SARS is “aerosolized through the sweat glands”, according to Dr. Hodkinson who gave his testimony to Reiner Fuellmich.

The patent reads: “In any of the various embodiments discussed above or herein, the antibody or antigen-binding binding fragment comprises a VH3-66 or Vk1-33 variable domain sequence.” This PubMed study reveals that “theVH3-53 andVH3-66VHgenesegments encode V regions“.

This PubMed study reveals that “Nucleotide sequences of the cDNAs encoding theV-regionsof H- and L-chains of a human monoclonal antibody specific to HIV-1-gp41“. So, monoclonal antibodies contain HIV-1 which is being encoded into your cells using cDNA. This is cross-species genomics! Also, the HIV-1 bioweapon is patented and owned by Anthony Fauci.

Another PubMed study reveals that the Novel V genes quoted above, do encode cells using mRNA.

Please see: Covid-19 Patent Horrors

Other horrors in the monoclonal antibody patent read: “isolated antibody or antigen-binding fragment thereof that binds a SARS-CoV-2 spike protein comprising the amino acid sequence set forth in SEQ ID NO: 832″…

A company called BacDive provides the “832” gene sequence which is a mycobacterium senuense05-832. It is an “aerobe, mesophilic, rod-shaped human pathogen that was isolated from sputum (mucous)”. This means monoclonal antibodies are lab-generated, bacteria based, chimeric pathogens.

Also mentioned in the monoclonal antibody patent is SEQ ID NO: 202. The “202” sequence patent says this is a “dystrophin gene” which is a nucleic acid being used for “gene silencing“ with “RNA interference”.

There is in fact so many genetic sequences mentioned in the monoclonal antibody patent that it would take days to break it down.

MARKER GENES & mRNA

The second monoclonal antibody patent #US10954289B1 states that marker/reporter genes are implemented using an artificial “Jurkat T cell line” and use Luciferase. This is an immortalized Human cell line that also contains insect DNA (Luciferase). That right there is cross-species genomics, aka cloning.

There are many patents listed within the monoclonal antibody patents. One patent in particular contains chimeric proteins that come from experimental humanized animal hybrid DNA. The patents specify that the chimeric proteins “can enter the cells and deliver the replacement enzyme activity lysosome”. The only way cell penetration is possible is if lipid-nanoparticles are used.

Another patent goes on to say that “recombinant RNA molecules comprising a sequence of a gene-editing molecule mRNA” is being used.

Monoclonal antibodies is a mRNA nanotechnology vaccine.

IMMUNE SYSTEM DESTRUCTION

Monoclonal antibodies target and destroy your body’s T-cells or killer cells while cloning a new hybrid cell line. Your T-cells are a vitally important part of your immune system and without them your body is left without any defense against disease. This will serve as the final nail in the coffin for vaccinated persons, or the “final solution” as Bill Gates calls it. Since the “vaccinated” are loosing 5% of their immune system every week, according to a UK Government study, they can’t afford to loose anymore.

The theory is that monoclonal antibodies suppress your natural immune system, enabling your B-cells to generate an antibody response to chimeric proteins. Do I need to explain how wrong this is? Doctors don’t believe it’s possible to detoxify “vaccinated” persons so instead they use their patients as lab rats for Big Pharma in unethical medical interventions.

Some Naturopathic Doctors like myself are succeeding to detoxify vaccinated persons. You can schedule a consultation with Dr. Ariyana Love (ND) or contact me for more information: metanutrients@protonmail.com.

Posted on by Ariyana Love

By Dr. Ariyana Love

(Updated January 11, 2022)

The U.S. Army just announced their new creation of a Spike Ferritin Nanoparticle (SpFN) “vaccine”, claiming that it works “against all existing COVID & SARS variants”. Without animal testing or safety studies, Human trials are already underway.

The U.S. Army published a series of preclinical studies claiming the Spike Ferritin Nanoparticle serum “protects against heterologous challenge with B.1.1.7 and B.1.351 virus variants” during an animal trial. This is key to understanding what they’re really doing with these death jabs.

“B.1.1.7” and “B.1.351” are literal genetic lineages that contain your God-given genetic information. Heterologous challenges result from cross-species genomics. When you delete genes and code Human cells with insect DNA (Luciferase) and monkey DNA, bad things happen. It’s called genetic mutation.

The official narrative explains that the B.1.1.7 Alpha variant of SARS-CoV-2, the supposed “virus” that causes COVID-19, has turned up in the UK and the B.1.351 Beta variant in South Africa. Then there’s the B.1.1.529 Omicron variant which is new on the scene. Now I’m going to explain to you how you’re being fooled because first they fool you then they rule you.

The CDC website mentions the “variant of concern (VOC), lineage B.1.1.7 is also referred to as VOC 202012/01 or 20I/501Y.V1”. Another page of the CDC website says about the B.1.1.7 variant, “This variant has a mutation in the receptor binding domain (RBD) of the spike protein at position 501, where the amino acid asparagine (N) has been replaced with tyrosine (Y). The shorthand for this mutation is N501Y”.

The key word in that quotation is REPLACED.

The Bullfrog

Look up N501Y and you find that it’s a genetic mutation resulting from reverse genetics (cloning). Reverse genetics involves directed gene deletions and point mutations (site-directed mutagenesis) to create null alleles (non-functional); which is gene knockouts. These gene deletions lead to permanent loss-of-function.

CRISPR-Cas9 – technology is raping your cells’ genome and cutting it at a specific location to allow genes to be removed and new engineered sequences to be inserted using RNA interference to permanently silence genes. Genetic knockdowns are typically temporary whereas genetic knockouts are permanent.

Moderna and other pharmaceutical bioterrorists researched extensively the knockout of genes in regards to “curing cancer” and what the reduction of amino acid asparagine (N) causes. The CDC says the amino acid asparagine (N) has been replaced with tyrosine (Y). When you knockout genes, the protein associated with that gene stops being produced by your cells. In this case it’s the amino acid asparagine (N) that has been replaced with tyrosine (Y) which causes rapid cancer growth. They want you sick and dying.

Gene deletion is also a behavioral modification that decreases your intelligence. It also serves to enhance receptor binding. Doctors must pay attention to this information.

The N501Ymutationis being induced by gene deletion, to cross the species barrier so that animal diseases (monkey disease) can create infection in Human cells that would not naturally occur. Since animal diseases do not infect Humans, cloning is necessary.

The UK Government says the “VOC-202012/01 variant includes 23 changes in the “virus” with eight mutations (changes) in the outer “spike” protein; nine changes that alter the amino acid sequence of proteins elsewhere in the virus genome, and six changes that do not alter the amino acid sequence of proteins elsewhere in the virus genome”.

What they are really talking about is YOU. Since viruses are still a theory and have never been proven to exist, governments and the pharmaceutical cartel are using the word “virus” to deceive the medical community and divert our attention away from their Bioterrorism. They want us to believe that a boogey virus mysteriously jumped from bats to Humans when actually they’re making changes to the Human genome.

This study confirms that SARS-CoV is nothing but “S glycoproteins” made using an unnatural genetic sequences that fools your cells into thinking it’s natural so your body will not reject the biohacking technology.

The Spike Ferritin Nanoparticle SpFN WO2021178971A1 patent, also confirms that the SARS-CoV is an “glycoprotein S” which is the “spike protein”.

So there you go, mystery solved. The infamous “spike protein” is not a “spike” protein from a “virus” after all. The glycoprotein S is a chimeric Bioweapon.

The SpFN patent also contains the transfection agent HEK293T/17 which is Human embryonic kidney DNA. It’s a chimeric “pcDNA” for cloning.

Thermo Fischer is using a “pcDNA cloning kit” which also does gene deletion.

The SpFN patent also contains HIV-1 which is patented and owned by the treasonous, mass murdering, Genocidal Anthony Fauci. It also has Luciferase (insect DNA) for tracking your every move. Oh yeah… and the patent confirms it came from Wuhan, China!

Aluminum Hydroxide is also listed in the SpFN patent and Aluminum Hydroxide is made from Graphene Oxide. They call it “Alhydrogel”. So… Graphene Oxide is irrefutably in the SpFN Bioweapon shots!

It gets even more disgusting. They’re using bullfrog DNA to create their chimeric glycoprotein “S”.

Who wouldn’t want to be transfected and cloned with bullfrog? Because if you don’t accept their Franken-vaxx, then you’re a racist… against the bullfrog species!

GENE DELETION

Studies show that the B.1.1.7 “variant” is directly caused by gene 69-70 deletion in Humans. The B.1.351 “variant” is directly caused by gene241–243 deletion.

The CDC openly admits that the Omicron variant is the result of an “S gene drop out” caused by “gene 69-70 deletion”.

The World Health Organization says that the S gene is not present in the Omicron variant. In its report titled “Classification of Omicron (B.1.1.529): SARS-CoV-2 Variant of Concern“, the WHO’s Technical Advisory Group on SARS-CoV-2 Virus Evolution (TAG-VE) confirmed that the RT-PCR kits which are designed to target the S gene, detect a complete dropout of the S gene.

Thermo Fisher’s Genetic Sciences Division revealed that the B.1.1.7 variant is the result of gene mutation caused by the gene deletion of the “S gene”. Thermo Fisher explains that the “S gene” is a 69-70 deletion. Thermo Fisher admits that gene deletion mutations is the cause of all SARS-CoV-2 variants, Lambda, Alpha, Beta, Gamma, Delta, etc.

Are you catching on? The “S” gene is the glycoprotein S Bioweapon, an artificial genetic sequence that’s being coded into Human cells (transfection/cloning) after gene knockout.

On their website Thermo Fisher also admits:

“The Omicron variant has been found to include the 69-70del mutation of the S gene, first identified as a mutation in the Alpha variant. This mutation causes a dropout of the S-gene target in results from widely used TaqPath COVID-19 Detection Kits. An S-gene failure does not mean a result is negative, only that the S gene was not detected. Multiple public health organizations have noted that this pattern of detection (i.e. S-gene dropout) can be used as a marker for this variant, pending sequencing confirmation.”

So there you have it. The PCR kits target genes for gene deletions and monitor the cloning progress.

All Covid vaxx patents mention gene deletion. Both Pfizer and Moderna claim their serums “protect against” the variants. The Moderna patent states it’s death jab is “folding proteins”. The folding of proteins induces genetic mutations.

The Pfizer patent directly states that it’s serum is deleting genes 69-70 and 242-244. So these lying bastards are not “protecting” against anything. They are inducing the scary variants through gene deletion.

Do not drink their poison.

The Pfizer vaxx patent also mentions the N501Y mutation due to but not limited to 69-70 gene deletions. Remember, 144 gene deletion causes rapid cancer growth.

Pfizer patent WO2021213945A1

Thermo Fisher owns the patent to a PCR kit that “targets genes”. The PCR kit is also a marker to “test” for gene deletions to determine if the jabbed are patent eligible.

Thermo Fisher sells the Microbeads used in the death jabs and markets them as Dynabeads and SPIONs. Then they have a PCR kit to “test” how their cloning project is going.

Cloning any species results in mutations that are unpredictable, as I previously documented in my articles here, here and here.

CONCLUSION

Variants are caused by gene deletion from fake vaccines and fake tests. Stop complying to your Democide and Mark of The Beast enslavement.

Serve the war criminals (anyone pushing the death jab) with Notices of Liability.

Contact me or book a free consultation and I will help you design a detox protocol that fits your needs and your budget, to remove the biological poisons we are being bombarded with. Do not loose hope because there are solutions to save and protect your health.