The Monoclonal Antibody Strategy

Get ready for monoclonal antibody targeted vaccines!

But first a refresher…

What is an antibody?

Human antibodies are Y-shaped molecules produced naturally by the body’s immune system. They recognise, bind to and neutralise specific viruses and other pathogens. – AstraZeneca, What Science Can Do.

What is a monoclonal antibody?

Monoclonal antibodies are lab-made antibodies that mimic what your natural antibodies are able to do, and are most often used as a form of targeted therapy for specific kinds of cancer, but they’ve also been used throughout the pandemic to help fight off COVID-19. – Cleveland Clinic, April 2023

Vaccine History

Vaccines were first developed under a strategy to stimulate and imitate natural antibody production in the body. This artificial manipulation of the immune system by scientists became known as Acquired Immunity (vs Natural Immunity). However, vaccine-induced, immunity is not long-term or reliable. A tell-tale artifact of vaccines is that their protection wanes overtime.

So, scientists set out to create a “new and improved” vaccine.

Enter the mRNA experimental COVID vaccines! These injectables are a mix of proteins from different viruses from the Family Coronaviridae. They are not designed to stimulate antibody production, because they are not true vaccines. Scientists call this gene-therapy. They are also being used as Cancer therapy.

Further, mRNA injectables are nanotechnology. They are emergency-use authorized, not FDA approved. The role of nanotechnology instructs the genome to create new proteins (antigens) not previously known to the body.

Unfortunately, the negative consequences of mRNA nanotechnology are many. mRNA jabs come with collateral damage that can dismantle the immune system. Some adverse events result in autoimmune diseases such as hemolytic anemia or Graves disease. Symptoms include premature aging:

This reduction in epigenetic clock estimates was significantly related to chronological age and immune cell-type compositional changes in B cells and plasmablasts pre- and post-vaccination. –Pang et al., Journal of Front Genet, June 2022

Enter the monoclonal antibody vaccine!

Monoclonal antibodies may be required for people who cannot develop or maintain an adequate immune response after vaccination. – Covid19 Prevention Network

The Nature of Healing: Heal the Body, Heal the Planet

by Rosanne Lindsay, N.D., M.A.

Monoclonal Antibodies: Ready, Aim, Fire

They are a type of targeted cancer therapy, which means they are designed to interact with specific targets. – National Cancer Institute

Monoclonal antibodies (mAbs) are a targeted platform, injected into the body. Think of it as a military-type, seek-and-destroy mission that picks up where the mRNA vaccine leaves off. The mAbs technology claims to specifically target a certain antigen for removal. In essence, mAbs counteract the effects of the first vaccines.

Specifically, where the mRNA vaccine encodes the DNA to create a foreign “spike protein” in the body, a SARS-Cov monoclonal antibody vaccine then targets that spike protein for removal.

There are dozens of new monoclonal antibodies soon to be released. A handy tracker of monoclonal antibodies in development for COVID-19 is maintained by The Antibody Society.

There are now antibody vaccines for colds and flus in development.

Why has there never been a universal cold and flu vaccine before?

According to Yury Bochkov, a respiratory virus specialist at the University of Wisconsin School of Medicine and Public Health, “Considering there are more than 100 types of A and B rhinoviruses, you would have to put all 100 types in one vial of vaccine in order to enable protection” against just A and B rhinoviruses.

In the cases of universal coronavirus and influenza vaccines currently under development, researchers have focused on more than just the surface protein, targeting other viral parts, such as the surface protein’s stalk, that are still detectable by our immune systems, but less likely to mutate from one variant to the next.

Will the strategy work or is it a pipe dream?

Natural Immunity is Innate

According to the human body, the natural immune system is already a thing of perfection. It comes as part of the human package, organically, through birth.

The body’s innate wisdom creates custom responses to the internal/external environments, at every moment, through two known poles of the immune system; cell-mediated responses and antibody-mediated responses. This dynamic system is referred to by western medicine as Adaptive Immunity.

The innate immune system adapts to changing stimuli for the best chances of survival. It can distinguish between different classes of pathogens and recruit the most effective form of adaptive immune response to target and eliminate them.

The ability to discern what is foreign from what is Self is an inherent feature of natural immunity. Thus, the body is able to create life-long immunity when it comes to most any infection. Vaccines, created in a lab, can only claim to stimulate an artificial antibody response. But when has that stopped scientific progress?

Maybe we’ll see a flu, COVID, RSV vaccine all combined in one.- Yuri Bochkov, respiratory virus specialist

The current flu vaccine is polyvalent, or quadrivalent, and contains adjuvants to stimulate an immune response, unnaturally.

The Risks of Injecting Antibodies (mAbs)

Monoclonal antibody therapies are described as “antigen based.” They are developed to be used in patients at risk for developing severe disease to decrease hospitalizations and mortality.

According to the government-funded, 2023 NIH study, “Benefits and Risks of Administering Monoclonal Antibody Therapy for Coronavirus (COVID-19)” there are serious risks for this group, including:

Monoclonal antibodies are EUA (Emergency Use Authorized], not approved. [where have we heard that before?]
As viruses evolve and mutate, mAbs become ineffective (fail to neutralize activity). This is the reason cold and flu vaccines do not work.
Adverse events such as transfusion reactions and anaphylaxis are documented.
As of January 2023, all previously authorized monoclonal antibodies have lost their EUAs for the treatment of COVID-19 due to the resistance demonstrated by this variant.
mAbs may promote selection for escape mutants.
Complications include infusion-related reactions are characterized by flushing, fever/chills, back or abdominal pain, nausea/vomiting, pruritus, or skin rashes.
Not authorized for use in severe illnesses requiring high-flow oxygen or mechanical ventilation due to this potential for harm.
Not indicated for patients with advanced age and/or underlying medical conditions that increase the risk of severe disease.
Not indicated for treating acute COVID-19.
Mortality is significantly increased in older, sick, people compared to younger healthy individuals.

This newly designed “antigen based” technology is the approach of the Gates Foundation.

Novovax™

One of many WHO-approved vaccines is Novavax, a booster vaccine authorized for adolescents 12-17. Side effects include: difficulty breathing, face or throat swelling, fast heartbeat, rash, dizziness and weakness.

Speaking as a doctor, [one expert] said that he has looked at studies of a vaccine called Novavax that does not use mRNA technology but is antigen-based, and he’s very encouraged by it….The next phase of the vaccination program will be to roll out the two-dose Novavax and other antigenic vaccines, in place of the mRNA vaccines. – LifeSiteNews

Questions:

Why create an artificial, injectable, monoclonal antibody treatment when the body naturally creates original antibodies?

Why create nano-antibodies that target antigens (proteins) purposely created by mRNA injections?

Is it to create long-term customers who lack an immune system?

RelCoVax™

Some proponents advocate a 2-antigen protein vaccine, aka, a second-generation multivalent SARS-CoV-2 vaccine. aka, a monoclonal antibody vaccine called RelCoVax. The developer of RelCovax, and a key architect of the mRNA vaccine, advocates a four-pronged approach:

1) Use the vaccine for those at highest risk, such as the elderly;
2) Provide early treatment to help keep people out of the hospital;
3) Provide tools for individuals to assess their own risk
4) Provide tools for individuals to test whether they have Covid.

Note: This is the same “four-pronged strategy” outlined by World Health Organization Director General, Dr Tedros Adhanom Ghebreyesus on March 13, 2020

WHO’s on First?

When the WHO downgraded coronavirus as a threat and cancelled the pandemic, it also said that thousands of people are still dying from the virus every week, and millions of others are suffering from debilitating, long-term effects.

Are the long-term debilitating effects, and deaths, from a virus or from a vaccine? Is the WHO getting ready for “another threat?”

Are you confused?

This type of clarity belongs to the likes of two comedians who once asked the question: “WHO’s on first?” Are we witnessing the Abbott and Costello comedy hour?

What Next?

Pipe dream or pipeline of nanotech jabs?

The pandemic strategy appears to be a 2-phase, Trojan Horse strategy, using 1) mRNA injections, as a first phase, and 2) antigen-based, monoclonal antibody injections as a second phase.

The W.H.O fails to warn about the serious adverse events of its strategies. These adverse events result from the experimental mRNA injections, as well as the risks of experimental mAbs already in use.

What ever happened to The Precautionary Principle?

the principle that the introduction of a new product or process whose ultimate effects are disputed or unknown should be resisted. It has mainly been used to prohibit the importation of genetically modified organisms and food.

The Precautionary Principle (PP), to many, is an approach that protects human health. To others, it is an obstacle to progress, and to pandemic-makers.

The nano, experimental injections coming down the pharmaceutical pipeline are described as an alternative treatment to vaccines. But it is up to each individual on just how far this experiment is allowed to go. This form of experimentation is a dead end for humanity, engineered by beings who have already reached their own dead end.

Humans are born, organically, to the life wave of the Earth. They are not created through genetic modification, so they do not need genetic manipulation to evolve. A higher form of humanity happens through spiritual transmutation over many incarnations. Not through divergent beings from outside this life wave who parasitically live off of humanity.

The New Religion

DNA manipulation and tampering does not equate to creation. Humanity does not evolve through hybridization. Humanity is a direct reflection of the Earth and of the Cosmos. As humanity evolves so, too, does Earth.

The idea that science can genetically manipulate humans into a higher form is a new religion. It is propaganda promoted by scientists who claim to have a divine right to rule over humanity. The ancient alien narrative, as human creators from another time, will be popularized, complete with ships in the skies. Watch for it.

What will you believe, and what won’t you believe?

Who is responsible for your evolution?

Are you?

Know who you are and where you come from, or your identity will be redefined for you.

Rosanne Lindsay is a Traditional Naturopath, Herbalist, Writer, and Author of the books The Nature of Healing, Heal the Body, Heal the Planetand Free Your Voice, Heal Your Thyroid, Reverse Thyroid Disease Naturally. Find her on Facebook at facebook.com/Natureofhealing. Consult with her remotely at www.natureofhealing.org. Listen to her archived podcasts at blogtalkradio.com/rosanne-lindsay.

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