The DNA Prime & Pair MOA of Auditing

Similar to how the Double Helix of Human DNA Genome is constructed, which is composed of two double strands, connected by 3 billion rungs comprising the genetic code, CytoDyn's Prime and Pair MOA also has two components integrally tied together. In this analogy, the two double strands are any ICI, either a PD-1 inhibitor or a PD-L1 inhibitor, while the rungs of genetic code holding the Tumor treatment ladder together, would be Leronlimab.

Why am I comparing/analogizing the genetic code/genome to Leronlimab? Because of Leronlimab's versatility. As we know, Leronlimab is a monoclonal antibody which specifically binds to the CCR5 receptor with greater affinity than our body's own CCR5 ligand, CCL5 or RANTES. CCR5 is widely used throughout the body in any disease which includes inflammation or infection. For a variety of purposes, CCR5 is produced whenever there is inflammation or infection. CCR5 spans across the gamut of disease processes, therefore it's inhibition via Leronlimab's blockade of CCR5, which actively displaces RANTES from CCR5, thereby leads to the inhibition of that same span of inflammatory and / or infectious disease entities. Similar to how the variations in genes produce the variety of phenotypes we appreciate between ourselves, which come as a result from the differences in the building blocks of a myriad of proteins, so too, the variations in the body's use of CCR5 in its various organs, also sits at the foundational origin and gateway of the huge variety and diffuseness of all the inflammatory and infectious disease entities.

When it comes to inflammation and infection, CCR5 determines everything. If you take a look at ohm's list, every disease in that list goes away if CCR5 was removed. CCR5 sits at the root of all of them. Just like genes determine everything, through their encoding of protein manufacture, from the color of the eyes to the function of the Immune System, so does CCR5 span the gamut of every inflammatory and infectious disease process. This is why when Leronlimab binds to CCR5, it interferes and blocks the processes necessary to allow that disease to propagate and is therefore analogous to the rungs of genetic code on the DNA Double Helix.

The function of the 2 strands of the DNA Double Helix is to store and transmit the genetic information. The most vital function of the two strands is the ability to replicate the DNA. The two strands easily unzip to form a template to build an identical duplicate of itself. Essentially, the two strands are essential for reading the genetic code in order to make proteins. Transcription is achieved when the strands separate allowing one strand to be the template for the synthesis of mRNA. (messenger RNA). Then Translation into a protein can occur when the Transcribed mRNA carries the genetic code out of the cell's nucleus to the ribosomes where it is Translated into a specific protein.

In this analogy, the two strands of the DNA Helix, are comparable to the ICI. This is because they permit and allow for the completion of what Leronlimab has already initiated and encoded for, which is the destruction of the Tumor. Leronlimab essentially has disarmed the Tumor by silencing RANTES. It has stripped the Tumor of its blood supply. It has caused a boat load of CD8+ Killer T-Cells to invade the Tumor MicroEnvironment and to attack the invading Tumor. By the time the ICI is introduced, the Tumor has greatly diminished in magnitude, as it takes several months for the Tumor to ramp up PD-L1 expression, but has not completely died. Certainly by then, it has greatly withered and faded away, but a few remaining Tumor cells have survived the CD8+ Killer T-Cell onslaught by activating their PD-L1 gene and these Tumor Cells now have the ability to convince the CD8+ Killer T-Cells that they are "actually" not Tumor, but rather, "in fact" are a normal cell which should not be destroyed. So, they have managed to survive by displaying a false PD-L1 ID Badge saying they're not Tumor, but "actually" self.

The MOA of the ICI is to inhibit PD-1 or PD-L1 depending on which ICI we're referencing. When the ICI is later introduced and once those Tumor Cells display sufficient quantities of their deceitful PD-L1 ID Badges, then their true identities become revealed. Their true self is seen when the ICI binds to either their false PD-L1 ID Badges, or to the CD8+ Killer T-Cell's PD-1, and this interference between the two, destroys this [Killer Cell to Tumor Cell] interaction. If there is therefore no interaction, then the CD8+ Killer T-Cell takes the safe route and kills the Tumor Cell, because it "assumes" that it is foreign. Therefore, the addition of the ICI permits for the complete destruction of any surviving Tumor Cells which thereby reduces Tumor Burden in the body down to zero. No evidence of Disease. NED.

In our DNA model, let's make one strand as PD-1 inhibition and the other strand to be PD-L1 inhibition. Two very powerful modalities that when administered to a patient Primed by Leronlimab to have a greatly weakened Tumor burden with elevated PD-L1 upregulation and increased CD8+ Killer T Cells in the Tumor MicroEnvironment, these ICIs become powerful enough to finish the job off and wipe out the Tumor in its entirety. Thereby completing and carrying out the original intention and programming put into place by its counterpart, Leronlimab. This is quite similar to how the DNA strands allow for the Translation of the Genome into proteins.

DNA has been around before it was discovered in the 1950s, except nobody even knew it existed. Just like this Prime and Pair MOA, has also been around, but only recently discovered. Leronlimab is essential to do the Priming. Without it, even a hot tumor won't respond fully to an ICI. Only in very rare and specific cases do Hot Tumors fully respond to an ICI, such as with that GSK Jemperli, (dostarlimab) and CRC Trial boasting 100% Cure Rate in a select, specific patient pool, all of whom, having a very specific gene. Leronlimab is initially required to greatly weaken Cold tumors by rounding up the Calvary of CD8+ Killer T-Cells, which then causes PD-L1 to get upregulated on Tumor Cells and then the ICI is brought on board to allow those CD8+ Killer T-Cells to recognize and destroy the PD-L1 clad Tumor Cells. If Leronlimab was not brought on board initially and if the Tumor is initially large and strong and PD-L1 being already high, the ICI might not work fully, because the Tumor is strong, and there might not be sufficient CD8+ Killer T-Cells fighting. The First step must be to greatly weaken the Tumor with the use of Leronlimab.

Since Leronlimab represents the rungs of the genetic code in our DNA model, then CCR5 Codons build the great variety of cancer disease entities encoded within the Helix. Disease comes from irregular and malfunctioning proteins, built by malfunctioning and irregular genes. Along the same lines, CCR5 is usually introduced when there is inflammation or infection, so Leronlimab's inhibition of CCR5 thereby inhibits disease. Death and dying is in the CCR5 code, but Leronlimab inhibits that death and dying.

Together, the Prime and Pair Helix is administered to stop cancer in its tracks and to reverse its progression to the point of its complete or near complete eradication from the body. This treatment is not water. It is not thin air. It eradicates the malignant Tumor from the body. Leronlimab + Any ICI for any Cold Tumor. Code correcting code. A DNA splice if you will. Tumor = malfunctioning genetic code, thereby producing mutant proteins of any organ etiology. Doesn't matter what the etiology is because Prime and Pair, Leronlimab and the ICI splice into CCR5 and PD-L1 which have not been mutated by the malfunctioning gene.

60 Trillion cells in the human body. Therefore, 60 Trillion nuclei and 60 Trillion DNA Double Helix, each 6' long, coiled genetic software, packed so small, yet packs the very program to produce a 6' man. 60 Trillion cells x 6' DNA = 360,000,000,000,000 feet of DNA per 6' man. That's enough DNA to go from the Earth around the Sun and back 300 times. That's what's necessary for a healthy man. You've got to admit, Man is Fearfully and wonderfully created. More info within each and every one of us than in every library on Earth combined. If there is a problem, 700mg Leronlimab weekly does the trick, finds the problem and together with an ICI, eradicates it.

Symptoms get exhibited if there's a problem with the Genome code. Signs and signals are produced when something is wrong. Prime and Pair find and locate the problem by searching out CCR5 and PD-L1. We can trust Prime and Pair because it has been tested and proven over and again. This work is not difficult for Prime and Pair treatment.

Any treatment that helps on the cellular level, that is where health is, where life is. When Prime and Pair find CCR5, that is the spark that turns up the flame. This treatment restores back the original healthy nature of the cells before they were cancer corrupted. How? They work at the molecular level. Sub-cellular.

In cancer, Health is only silenced. It is not lost. Health can be restored. It becomes the regeneration of what disease has destroyed. A Transformation back into the future. This is Not going forward, but backward. With Prime and Pair treatment, the patient goes back to where they were before the Tumor arrived. Their original body restored. What does the all the work? The Immune System. Nothing new is under the sun. What has been shall be again.

The DNA spells out instructions on how the body should function, how to sweat, how to pee, how to digest. It gives these instructions in order to live. Without these instructions, or if there are problems, then death begins. The body only works according to DNA's original instruction. For a good long, healthy life... those instructions are in the DNA. Don't add to it. Don't take away from it, for it is perfect, but when it mutates, then that's a problem. We just have to get back to the original program and Prime and Pair does exactly that. DNA copies the original from one cell to another, flawlessly. Prime and Pair brings us back to the original via splicing into and activating the Adaptive Immune System. This is how to understand what Prime and Pair does. It brings the body back... naturally. Now, we have come to see the details.

Good bye Tumor, thanks to Prime and Pair. This is the path back to the original. 20 years on this path through the miry clay. But this has been unveiled, what has already been here all along. Today, CytoDyn writes this, no, Engraves this, already written MOA into the Trials of stone making the output of healed patients to be permanently Engraved, thereby bringing back what already was.

Nobody is a blank slate. Everyone has already been written on with code. Prime and Pair undoes Tumor's re-write of the Genome. These eINDs are now under Renovation, who were once under Tumor's rule and reign, are now instead, brought back up, delivered home, Northbound, brought forth, and Published as healthy survivors with NED.

What does the re-writing? Prime and Pair, CytoDyn's Tumor treatment. Once administered to the point that the Tumor is eradicated, it becomes a permanent eradication. Why? The Adaptive Immune System then produces Memory T-Cells which recognize the same exact cancer before it gets a chance to be re-established again. Following Prime and Pair, the Cure is written and imbedded within the patient. The effects of Prime and Pair are written into the very memory of the Adaptive Immune System of the patient. Since these patients have been treated with Prime and Pair, they learn to do by nature, the same things that were done under the treatment. Prime and Pair facilitates biologic teaching. The law gets written into their innards because their Adaptive Immune System was awakened by Prime and Pair. None of this can happen without Leronlimab because without Leronlimab, Memory T-Cells are not even created, because RANTES prevents Adaptive Immunity from happening. Remember, RANTES shuts off the T-Cell response.

Each and every patient who responds to Prime and Pair is a Publication of this DNA MOA as the patient Yields and heals due to this treatment. Why? Because their healing response is the output of Prime and Pair in action. Without a patient, all it is, is biologic molecular code. Every patient, who then becomes a cured patient is a Witness and a Publication of the DNA MOA. That is Prime and Pair's story.

Why is Prime and Pair, as it were, suppressed and hidden? Because every great book, is written in private before being written in public. Every great manuscript is hidden before a publisher finds it. Preserved for Publication, the once sick but now healthy Witness.

The hardest part of writing a book is Editing. Painstaking work. Eradicating the errors. This is the process when the patient undergoes this treatment of Prime and Pair. The Editing process of Eradicating the Tumor. But, Prime and Pair treatment is made easier due to the very fact that Leronlimab is on board. Chemotherapy may not even be necessary. The good work gets performed to the point when Memory T-Cells are produced. End of Story.

Witnesses are a story of perfection as their Adaptive Immune System has been perfected at least against their disease. All the patients in the eINDs participate with Prime and Pair and should they follow through to completion, then they return back to the original pre-cancerous body. The story is written for them, should they complete the treatment. Prime and Pair brings them back home through the molecular Editing of their Immune System.

We are about to hear from a multitude of patients about their stories, about what they've been through and that nothing else has helped them before, until Prime and Pair delivered them back to the original. Not to new content. Rather to delivered up, healthy content, restoring the original intent of the Author. The result is a Publication of what was already there in their inward parts via Prime and Pair's Auditing capacity. It shall all be made known.

This is a test of time that proves to the world what Prime and Pair is. The world awaits CytoDyn's Unveiling of Prime and Pair. The Publications, the Disclosures and the Unveilings are coming of the eIND patients all resulting from Prime and Pair DNA MOA. The book is being written with each patient brought forth. You don't have to go far to find such saved patients. They shall do exploits. Books almost ready to be published. When these stories are Manifested or Unveiled via Prime and Pair. Then the public shall know what the life of the DNA MOA of Prime and Pair actually is, coming through Phenotypically in the saved lives of these Witnesses. The manuscript of Prime and Pair, Written in secret, gets Unveiled to the public. Each eIND is a Witness to the DNA MOA testimony of Prime and Pair, a Permanent Witness with NED.

These Witnesses have been Engraved. Unable to be erased because Prime and Pair writes with Permanent ink. Prime and Pair works with our already written but Tumor corrupted code. The original code was broken by the Tumor. The DNA code of Prime and Pair restores back the original which then becomes an Indestructible code, an Engraved code forever. A reproduction of the original.