To get an idea of who these people are, here is the Jew World Order bio.
“Jewworldorder.org is not a website to spread hatred, violence or racism.
“The truth has no agenda.
“This website was created by a group of true Semites and Hebrews, concerned about the state of the world, who wish to spread the truth to the people, about the criminal murderous edomites/canannites/khazars/Turks, that fraudulently call themselves Jews.
“Bloggers and Publishing Networks emailing me to get their articles published on my website, are welcome to publish their articles, so keep sending them, and we will keep publishing them.
“We support the true Hebrew Israelites not the fakes that call themselves Jews today.
“Jewworldorder.org is a website for truth seekers sick and tired of the lies spread by our Jewish Mainstream Media Networks.
“We have so many haters of this website. All of them are Zionist Jews. So don’t be surprised to see fabricated stories about any of our team members on the internet. Zionist Jews are brilliant at deception and defaming the innocent. This is the sole reason why the Jews own the Media News Networks all over the world, to tell you how to think, and who to hate, for their evil global agendas. (Divide and Conquer) it’s how they brought down many ancient civilizations in the past and modern ones today.
“Jews are Mongrels, they have been proven many times to be an invention. Even their Genetics have been tested and found to contain many many races… since they migrated from their motherland Khazaria / Ottoman Turkish Empire long ago. Jews were the original Gypsies, that went from country to country, village to village. Stole, killed and kidnapped children, for their satanic rituals.
Before you go and pigeonhole CIN as an anti-Semitic rag, let me make one thing crystal clear… Semitism is the root form of language. Semitism is not a race at all… The biggest truth is that all languages, spawn from Semitism…
That’s right! All our languages derive from Canaanite.
It’s Babylon, baby!
To say anti-Semitism, is to say anti-language or anti-literate… and believe me, I am totally pro literate.
Besides, Ashkenazi is a mixed race, it’s a political mafia of Nazi Jews. Gaslighting ends here.
Now, on with the show…
CCR5 gene is the door to your immune system. Cancer requires CCR5. COVID requires CCR5. HIV requires CCR5, … Those with a “mutation” don’t catch certain Cancers, COVID or HIV, … Odd that the Ashkenazi Jews have the highest rate of the CCR5 mutation. Up to 10% of European’s have this mutation. Highest rate in the Ashkenazi population.
Is it not curious that this evolutionary mutation has left some races more superior? Is this Darwin’s survival of the fittest at play or the Satanic Scientists at Fauci’s Fort Detrick?
What happens if you don’t have CCR5?
The CCR5 delta 32 mutation, which was discovered over 20 years ago, disables the CCR5 receptor on the surface of white blood cells. HIV uses this receptor almost like a key — it latches onto it to get into the cell. Without a working version of CCR5, HIV is essentially locked out of person’s immune system.
These conclusions are consistent with the fact that the plagues, like the CCR5-Δ32 mutation, were confined to Europe. The CCR5-Δ32 containing ancestral haplotype was estimated by the use of coalescence theory to have originated around 700 years ago (range 275 to 1875), coinciding with the date of the Black Death. [Which CIN does not buy, but we’ll get to that.]
CCR5 is believed to offer protection against the Bubonic Plague.
CCR5 is believed to offer protection against HIV, gp41 and gp120.
CCR5 is believed to offer protection against Cancer sv40, gp160.
CCR5 is involved in memory, addiction, depression and fear.
CCR5 is believed to offer protection against COVID.
CCR5 is believed to offer protection against Dengue Fever, HPV, Hepatitis, Polio, Ebola and Marburg.
Rickets, a vitamin D deficiency disease. It seems those of us with the CCR5 gene also have more Vitamin D receptors! Which means we need more vitamin D than the Ashkenazi’s!
Are you seeing a pattern here?
A Little History:
The National Center for Biotechnology Information (NCBI) provides a large suite of online resources for biological information and data, including the GenBank® nucleic acid sequence database and the PubMed database of citations and abstracts published in life science journals.
The GenBank was started by The Los Alamos Laboratory and maintained by Robert Gallo’s NIH.
The gene banks is Robert Gallo.
Robert Gallo holds the patent to an HIV vaccine that uses the Poxvirus. The theory on CCR5 mutation speculated whether it was the Bubonic Plague or Smallpox that brought about the mutation. I think it was always the smallpox vaccine. That’s what they say caused HIV in Africa. Gallows owns the patent via Connaught Medical Research Laboratories.
If you cause the mutation using Smallpox vaccine, for example, generations would start to develop health issues. Then you introduce different diseases… Polio delivers sv40 leading to Cancer…etc…the immune system is wide open.
Smallpox was declared eradicated in 1980 by the World Health Organization (WHO), and the WHO was the one who delivered the Smallpox vaccine to the entire planet. That had to be the CCR5 mutation.
Here they say the Smallpox vaccine may have opened up a dormant HIV virus in Africa.
Even when we assumed that the resistance allele was dominant, we found that bubonic plague could not generate sufficient selective pressure to account for current CCR5-Δ32 frequencies, despite the periods of unprecedented disease mortality. The 400-year period of plague epidemics in Europe did not remove enough individuals of high reproductive potential to generate a sufficient selection coefficient. Our results suggest that plague could not even have driven the resistance allele to 1% during the period that it existed in Europe (Fig. 1). However, we found that the more continuous smallpox mortality that afflicted European children since the origin of the allele could have provided the necessary selective pressure to generate the rise of CCR5-Δ32 deletion to current frequencies of 10% (Fig. 2).
You get two genes, one from each parent, they call them alleles. Some children are born with two “mutant” CCR5 genes or alleles. Some offspring may get one gene or allele. If you have two you are CCR5 dominant, if you have one you are CCR5 recessive. Not everyone will have two. Those with two CCR5 genes will have superior traits.
I am referring to CCR5 “mutants” here. But again, they are not mutant genes, we propose they are healthy genes and it is our genes that are mutant. Again, it may not have been the Plague but Smallpox vaccine campaign that drove that CCR5 mutation.
We have a mutated gene, THEY have the healthy gene.
The WHO went everywhere and vaccinated everyone on the planet.
Smallpox, a virus in the same family as Myxoma virus, has been infecting humans for thousands of years – the earliest outbreaks are believed to have occurred before 1000 AD. The receptor for Smallpox virus is not known, but if it is CCR5, then smallpox is the leading candidate for the selective pressure responsible for fixation of the CCR5 delta 32 HIV-1 resistance allele in modern Caucasians.
Myxoma is like smallpox and it uses CCR5 to attack the immune system.
If they used the Smallpox vaccine to cause a mutation specifically at the ccr5 receptor. That would weaken us…our children too.
The CCR5 mutation results from a 32- base pair DELETION from the CCR5 gene. Those carrying the mutation are show SIGNIFICANT resistance to not only HIV but also Smallpox. THAT BEING SAID IT IS HIGHLY PROBABLY THAT THE NWO MANUFACTURED THEIR OWN NATURAL SELECTION.
The evidence strongly demonstrates that the small pox vaccine was the delivery route for the ccr5 mutation. As you can see in the following global population graph generated by the United Nations, population growth was proceeding exponentially.
WWII caused a decrease in global populations which the NWO assumed would slow down overall population growth. However, this was not the case as a population bubble occurred post WWll with what is now referred to as the baby boomers. Hence global wars could not contain or slow down the planetary exponential growth rate that would mist definitely put a strain on all earth resources especially water. So it’s not surprising that following WWll the NWO started mandating the small pox vaccine which we believe altered the human genome, specifically mutated the original CCR5 gene; the doorway to your immune system.
As you can see population growth rate decreased as a result. Is it not surprising that cancer rates, autoimmune diseases and inflammatory diseases started an upwards trajectory? Indeed the human genome has already been corrupted and we are the genetic offspring of all those that took the small pox vaccine.
The CCR5 delta 32 mutation seen in the Ashkenazi population is therefore in fact the unmutated intact human genome. Later the COVID vaccine was then used to stimulate a further decline in population while implementing their mind control protocols into the general population. They are studying your biometrics; they see and know everything you do. And harvesting your consciousness is their next mandate. You are slowly being corralled into their matrix called Eqoria.
HOW? Robert Gallo’s Fort Detrick, under the supervision of Kissinger and his CIA-MK-Ultra goons, was home to the world’s “reverse transcriptase” research.
THESE ENZYMES ARE CAPABLE OF CONVERTING RNA SEQUENCES TO cDNA sequences that are capable of inserting into different areas of the human DNA genome. OUR THEORY implies they inserted 32- base pairs into everyone’s DNA specifically at the CCR5 gene creating a new CCR5 gene in the human population. And in actuality, the true mutation is the CCR5 gene that the majority of humans have and the CCR5 delta 32 mutation missing the 32 base pairs is actually the preserved human genome.
And how was this carried out? Through the world-wide vaccination of Smallpox sanctioned by governments and the United Nations! THEY MUTATED THE HUMAN GENOME BY ADDIND 32 BASE PAIRS AND KEPT THEIRS INTACT. SO WHAT THEY REFER TO AS THE CCR5 MUTATED GENE IS IN FACT THE INTACT UNALTERED HUMAN GENOME!
I would day this theory is insane…but they are all the same actors!
It was Robert Gallo that started working on finding human retroviruses in 1970, prior to the implementation of the human genome project in 2002 and the “discovery” of the CCR5 gene in 1996. So, is there really a mutated CCR5 gene resistant to HIV, COVID, Smallpox and certain Cancers? Sure….but it was never mutated….it was always the original unaltered genome and the sheeple get suckered into vaccines that altered theirs while the global elite built up their coffers on the Cancer, HIV and COVID industries!
Robert Gallo and the Patent on ccr5 gene:
The patent decision “takes my breath away,” says Robert Gallo, director of the Institute of Human Virology at the University of Maryland, Baltimore. “As a society, we have to ask if it’s fair” to give the main commercial prize to the company that sequences a gene rather than to those who do the hard work of figuring out its biological function, says Gallo.
Ironically Robert Gallo and Anthony Fauci lead the research at Fort Detrick.
Several groups, including Gallo’s, that played critical roles in identifying the suite of receptors that HIV uses to slip inside cells have also applied for patents, but their claims were filed after HGS’s.
Who is Human Genome Sciences? Bought out by GSK in 2012.
Robert Gallo was also working on the CCR5 receptor! But, aw shucks, he didn’t make it to the patent office on time.
All the theatre out of Fort Detrick:
Henry Kissinger had a heavy hand in the Club of Rome and operations out of Fort Detrick. His Jewish name was Abraham….Chabad! He set the whole thing up!
Kissinger’s Master Scientists:
Robert “Final Solution” Gallo
Jonas “Mutate Humanity” Salk
Albert “Painless Polio Jab” Sabin
We can do this all day.
NWO Shell Game:
DID YOU KNOW? The Chinese biological laboratory in Wuhan, Wuhan National Biosafety Lab, is owned by GlaxoSmithKline. Glaxo coincidentally also merged with and owns controlling stakes (68%) in the company Pfizer, which is currently developing a C0VID-19 vaccine. Pfizer coincidentally manages the finances of a company called Black Rock. Black Rock coincidentally also owns stakes in both Pfizer (8%) AND AstraZeneca (6.8%), another company currently key in developing a C0VID-19 vaccine. GSK also has controlling interest in the Sanofi vaccine… and Sanofi is China through Blackrock and Vanguard!
Rothschilds Chinese Pharmaceutical Circle Jerk
Who has the cure?
What are examples of CCR5 antagonists (drugs)?
The current leading CCR5 antagonists in clinical development include maraviroc (UK-427,857, Pfizer), aplaviroc (873140, GlaxoSmithKline) and vicriviroc (SCH-D, Schering-Plough), which have demonstrated efficacy and tolerability in HIV-infected patients.
GSK all the way!
Anthony Fauci/NIH Speaking about turning off the CCR5 gene to treat HIV……. Anthony Fauci, M.D., director of the National Institute of Allergy and Infectious Diseases (NIAID), told Science magazine: “There are so many ways to adequately, efficiently, and definitively protect yourself against HIV that the thought of editing the genes of an embryo to get to an effect that you could easily do in so many other ways in my mind is unethical.”
Is GSK merging with Pfizer?
On 1 August 2019 we announced that we’d completed our transaction with Pfizer to combine our consumer healthcare businesses into a new world-leading Consumer Healthcare Joint Venture.
So who owns the CCR5 gene? The key to your immune system? The NWO of course.
Who owns the cure that will shut the door?
Boom….the CCR5 receptor is on GP41….it was on the Enzolytic site….so yes…those auto antibodies ITV-1 are the cure for everyone with the CCR5 gene.
Let’s not forget Cancer, they build two industries from their twisted science. HIV and Cancer. Now Enzolytics is coming in for the win.
Enzolytics is a rabbit hole that leads back to Club of Rome in Bulgaria.
sv40 discovered in COVID jabs. Controlled Opposition say it’s contamination. But sv40 is part of the binary delivery system.
There are sv40 delivery vectors that can target CCR5.
Science seems to be working incrementally with this group. Just tell people to live in fear, and that they are all going to die. Let’s rephrase Kevin McCairn’s tweet; “sv40, contained in the COVID jabs, readily integrates Clathrin through CCR5 receptor”!
They knew it was Clathrin allowing viral entry even for Smallpox using CCR5 receptor.
Our modern understanding of endocytosis comes from two important observations made in the 1970s. The first was by Ralph Steinman and his colleagues who used quantitative biochemical and electron microscopy approaches to demonstrate that mammalian cells in culture were able to internalize enormous amounts of the plasma membrane. These scientists made the important observation that most of the membrane that was internalized was later recycled back to the plasma membrane (Steinman, Brodie & Cohn 1976).
Ralph Steinman discovered Clathrin transport. He also discovered the involvement of dendritic cells (this is the receiving top part of the neuron) are involved in immune system regulation specifically T cells and they are also required for the activation of vaccines!
Steinman was funded by NIH grants…in Canada! Here he connects the dendritic cells that activate the immune system via vaccines to CCR5 activation.
Steinman knew dendritic cells could proliferate HIV infection and HTLV infection… the leukemia virus Gallo was working on.
Steinman was working at Rockefeller University when he got those NIH grants.
He was also a corresponding fellow of the Royal Society of Edinburgh. In 2012, the Ralph M. Steinman Center for Cancer Vaccines was established in his honor at the Baylor Institute for Immunology Research in Dallas, Texas.
Steinman was a trustee of the Trudeau Institute in Saranac Lake, New York. He also served as a scientific advisor to several organizations including the Charles A. Dana Foundation, the Campbell Family Institute of Breast Cancer Research in Toronto, Canada.
Royal Society of Edinburgh.
Steinman was the lead in Rockefeller/NIH research, millions in research for vaccines.
Gates foundation funded Steinman’s research.
The founder of this research was Dr. Zanvil Cohn….Over the course of his career, furthermore, Cohn served as “adviser or trustee of Harvard University, Massachusetts General Hospital, Max Planck Institute, Trudeau Institute, Roswell Park Memorial Institute, the National Institute of Allergy and Infectious Diseases, the New York Blood Center, and Bates College.”
He was Steinman’s mentor! Both Trudeau Institute!
Started in 1884 by Dr. Edward Livingston Trudeau. “Our Trudeau Research Network—comprised of highly-trained research teams who all study some aspect of infection and immunity across a variety of different pathogens—works closely with collaborators to bring translational science to life. Our studies focus not only on immune responses to major infectious diseases, such as TB, influenza, and Zika, but also on the role of the immune system in cancer, autoimmunity, and aging.”
Same family tree, the Trudeau’s!
This ties in the Insurance Cartels, and Aga Khan! This is one big CCR5 Mafia!
And get this, Pegalated GO gives you a more profound response. So the drugs the vaccines all with PEG GO.
I believe they were always targeting our immune system. That why there have been more autoimmune diseases, more Cancers. Lupus, MS, Arthritis… LoL, my favourite, Fibromyalgia. The ”everything is wrong with me” disease… POTS is the new one. That’s the vaccine…
Oh, and those lovely GO nanoparticles are supplied by our dear friends at the Trudeau Foundation.
Clathrin Neural Lace:
Gallo is CCR5. Steinman is Clathrin. Vitaliano weaponized it all.
We demonstrate that agonist binding triggers clustering of cell surface CCR5 into Clathrin-coated domains of the plasma membrane containing the adaptor protein complex 2 (AP2). CCR5 molecules are then internalized through Clathrin-coated pits (CCPs) and CCVs into early endosomes together with transferrin (Tf), a marker for the Clathrin-mediated endocytic pathway. By suppressing the expression of Clathrin heavy chain (CHC), and the formation of Clathrin-coated structures, we establish that Clathrin is required for ligand-induced CCR5 endocytosis. Finally, we show that cholesterol can influence agonist binding to CCR5, but we find no evidence to support a role for non-Clathrin-mediated endocytosis CCR5 internalization.
Seriously, Clathrin acts differently with those having the CCR5 gene.
GSK was a major funder of Obama brain initiative. Vitaliano’s Clathrin Neural Lace headquarters.
Clathrin is CCR5 dependent… BOOM!
This explains it all!
They always catered around the CCR5 gene.
Science says that MAYBE the mutation occurred during the Bubonic Plague but more likely with Smallpox. They have nowhere to show it mutated 700 to 1400 years ago… But hey, say it happened long ago, and people will ignore it, right?
They controlled all the data and gene banks massive coverup indeed but they controlled the human genome project…and they found the key to the immune system!
All this was is an elaborate money laundering scheme to use tax dollars to line their pockets all the while setting up medical industries where they caused health implications to the general population in order to control them and sustain these profit based industries.
The scary part….remember what the club of Rome guy Said…people will run for the cure….at the end there will be a lit of CCR5 mutants that don’t belong to their exclusive club…the estimation is 1 to 10% of Europeans with this mutation …so people will run for a cure they do not need….if you survive what they are planning you don’t need it.
My guess is this cure comes with their Intel chip? Because Clathrin nanotechnology will not work on CCR5 mutants.
Ya…the Matrix looks pretty good right about now
That or enslavement?
Race Based Weapons:
Viking History to the Royals, Knights Templar, Jesuits, birth at Roslyn, Scotland. Cloning & Transhumanism originated at Rosilin Institute lead Eugenicist. The scientists will lead you to Salk, Gallo, Fauci. Follow Dolly, VISNA, HIV, Polio, Covid.
The average frequency of the CCR5-Δ32 deletion allele is estimated to be 10% in European populations, but it is virtually absent among native subSaharan African, Asian, and American Indian populations.
Who has ccr5 gene mutations?:
Ashkenazi Jews! Chabad!
Although the Chabad movement was founded in Eastern Europe, a center of Ashkenazic Jewry, it has attracted a significant number of Sephardi Jews as adherents in the past several decades. Some Chabad communities are now a mix of Ashkenazi and Sephardi Chabad Hasidim.
Seems easy. ESPECIALLY considering the control the sequence flow through NCBI. Or their labs in Ukraine?
And we’ve been joking Gas Chambers No Longer Required.
Robert Gallo is known as the king of retroviruses….he could have added those 32 bases to their CCR5 genome…through vaccination giving them the protection they needed against disease. I do not believe fir one minute that the principle ccr5 researcher…the principle hiv researcher and the principle smallpox viral researcher and the principle retroviral researcher on the planet… which discovered the ccr5 gene is the door to one’s immune system….would not purposely create a superhuman class. There are only two possibilities… either our ccr5 genome was altered …or theirs was. And they built their empire by making billions of people sick. Natural selection would have taken millions of years…and the ccr5 gene mutation was far too specific!
Natural selection would take millions of years!
It takes time for a single change, let alone 32 in the sweet spot.
A stem cell transplant from a CCR5 supremacist will cure you.
Maraviroc is the drug …anti CCR5…inhibits CCR5 receptor… HIV-1 glycoprotein 120.
Inhibiting CCR5 with that drug prevents neuronal damage and behavioral impairment.
Conclusion. Our findings suggest a role for a hippocampal CCR5/RANTES axis in contextual fear
memory consolidation; in fact, RANTES levels increased at 12 and 24 h after CFC training. When CCR5
was blocked by maraviroc before CFC training, RANTES (hippocampus), corticosterone levels, and
fear memory consolidation were greater than in vehicle CFC-trained rats 24 h after the CFC session.
Remdesivir will also target CCR5.
DMSO inhibits CCR5.
Now some words from some true racists…