Virology and Lie-ology

Virology and Lie-ology

The latest stream (7.5 hrs) from Dr Kevin McCairn I concentrated on his analysis of the following article, mainly because they are still insisting in the scientific journals like Nature and Lancet  on the blatant lie  that the virus is zoonotic.   They made and released a bio-weapon and are lying to your face.



Virology and Lie-ology (30 mins)

Ah, those were the days (lolz)


If you want to watch the full unedited version then join the Dojo:

In the second part of the video Kevin analyzes the Eric Weinstein mea culpa which although it is a year old is quite funny.  Me thinketh he doth protest too much.

Eric Weinstein is the brother of Bret Weinstein. Eric Weinstein received his PhD in mathematical physics from Harvard University in 1992 under the supervision of Raoul Bott. In his dissertation, Extension of Self-Dual Yang-Mills Equations Across the Eighth Dimension, Weinstein showed that the self-dual Yang–Mills equations were not really peculiar to dimension four and admitted generalizations to higher dimensions. Weinstein left academia after stints at the Massachusetts Institute of Technology (Epstein was funding MIT projects) and the Hebrew University of Jerusalem. More than 20 years later, in 2013, he announced a potential unified theory of physics.

It is cringe worthy to watch. Everything from his dual citizenship, his links to Epstein his pathetic excuses. The only excuse he didn’t make was that of lawyer Alan Dershowitz (another Jew)….I kept my pants on during massages (lolz).  The girls involved were not minors (although very young) because this was Epstein’s NYC apartment.  His Caribbean  Island was another matter. The point is that all these scientific networks were involved with people like Epstein. They were all getting money from him.  Like Kevin says, perhaps Weinstein was innocent but he moved in those circles and must know people who were involved. Why has he not come forward?  Why has no one been arrested?  The whole system is utterly corrupt and they are covering for each other.

Go to the Dojo if you want to watch the analysis.   The point is not the guilt or otherwise of Weinstein who is scrabbling to distance himself.  The point is that all the systems are corrupt. Epstein had even hooked the Royals.   The take-away is … can you trust anything that comes out of these scientists mouths. This was the original monologue –

I didn’t do nuffin (lolz)


FDA Approved

FDA Approved

The FDA has approved the vaccines which means that they can now be mandated because they are “safe”.    I have placed a full five our stream from Dr. Kevin McCairn below.  I had no time to edit it down etc.  If you watch it from the beginning don’t be offended by the memes…they have actually been highly effective.

So far I have only watched the first hour and I have taken a clip of the CDC CEO Walensky to tweet out (see below).  The section about the Rev Jesse Jackson is funny.  He literally has rainbow turds on his mouth (lolz).   The world has truly gone mad.


The insidious face of a pandemic of variants

Geert warned more than 2 months ago and no one listened.

Dropped into the Bat poo

Dropped into the Bat Poo

This is edited from a recent 4.5 hr stream.  In the first part Sharri Markson from Sky news interviews Ian Birrel about the lab leak (origin) and in the second part Kevin analyzes the Zenodo article.

They dropped you into the bat poo (1hr 43 min)

Zenodo article:

Kevin’s article:

Bat soup or bat poop?

Bat soup or Bat poop?

That is the question that has been exercising the minds of our top scientists.  Is it soup or poop? (lolz).  Is it natural spillover or was someone swabbing a bat butt? Did someone eat a bat or play with bat poo?

I think we know the answer now.  We have truly rattled their cage and the criminals are getting scared now.  They are changing the story.  Damage limitation. An accidental leak. Sorry, I am not buying it.



Send in the marines (Rixey)

Send in the marines (Rixey)

Anyone who takes time to look at the work done by ex-marine and WMD investigator Charles Rixey can see that the wheels are falling off their narrative.  The Beast is exposed and we must go for the soft underbelly.  Make no mistake we are in the belly of the Beast but we possess the sword of truth and the determination to cut our way out of that lugubrious bloated belly.

And then there is this:

Joe Rogan speaks out

Joe Rogan speaks out


Rogan is popular and has a huge platform.  This is breaking into the mainstream now.  The truth will out.

Breakthrough Cases and Vaccine Passports

Changing narrative

It is falling apart before our eyes. The emperor has no clothes. Even the dumb masses can see that the emperor is naked. You just watch the narrative change.  You can expect a massive move towards war because they cannot admit how corrupt the institutions have become.  They will blame China.  Millions will die and they will make off with the loot again….and they get to write the history books again.   Not this time.  Not this time. 


UK Column is Fifth Column

UK Column is Fifth Column

I am afraid that I am going to have to call out the UK Column as a Fifth Column. What else can I do?  It is with a heavy heart but they have expended their goodwill. It must be obvious to anyone with eyes that Henningsen is IIA (Interactive Internet Activities).  He has been leaned on.   The one thing that you are not allowed to say is that covid is a bio-weapon and that it had a lab origin.  I offered the crew an opportunity to debate and discus it. No answer. Instead one of the members responded that it was a conspiracy theory (like Hennigsen did).  The irony of Alt Media calling someone a conspiracy theorist is exquisite:

It is not a “theory” how can it be a theory when the genome has been sequenced? We KNOW that it was made in the lab (lab origin) and we KNOW that Ft Detrick and China have data missing so that it can no longer be traced. But the EVIDENCE is in the genome itself and then there is the murder suicide and disappearance of bio engineers geneticists etc. Low level bio-war has been ongoing for decades. They have been funding this for decades and trying it on. Look at the history of the first pandemic SARS-Cov-1. Are they lying about PCR and death numbers? YES. Are they promoting fear? YES Are the vaccines dangerous? YES. Unlike Patrick I will not let these bastards off the hook. Saying that it originated in a lab is the ONE THING that gets you attacked from ALL SIDES. Both the alt media and the MSM attack you when you dare suggest that they made it in a lab. We are to believe that someone ate bat soup and had pangolin as a side dish? Transgenic humanized mice were used, but meh! natural. I KNOW THEY MADE IT AND RELEASED IT. And I will expose the bastards and their fear/propaganda campaign. The virus/vaccine was designed to trigger inflammatory pathways so that they can gather data for their transhumanism project. They want you to believe that the virus is not real. If you believe it is a figment of imagination…a computer printout….a propaganda phantom then they have got you where they want you. They have run a brilliant misinfo campaign. Hats off to them.

And this:

And why no reply from Patrick, or Mike or anyone on the UK column? I have supported them since the beginning. Why no response? This issue is crucial. Why don't they arrange a debate then? I can bring a number of PhD. neurobiologists and WMD experts and DRASTIC members and researchers to the table. A video by "Kaufman" who admits he knows "nothing about viruses" and charges $1700 for a private that your source? You rely on a conman who says that no viruses exist at all? Germ theory (laughable) or perhaps Dr Sam Bailey who Patrick refers to. Promoting her book. All grifters. Ask yourself this why are they allowed to continue? Why do the algorithms promote their channels? And yet Kevin gets his Discord server nuked and all his followers thrown off? They even publish counter articles in Nature and the Lancet. Why is that do ya think? Have they done that for the UK column?

So there is the challenge.....debate the central issues:

1. Lab origin
2. Who is behind it
3. Why are they doing it

Anything else...masks, lockdown etc is just distraction. They are important but they are side issues. You are being led away from the truth.

So, debate? Any answer?

There was no answer forthcoming so as far as I am concerned they are fair game now. One by one they are showing their true colors.  Alex Jones, Whitney Webb, Last American Vagabond, UK column,Gab the free-speech platform. This list is by no means exhaustive. Just about everything is false.They are limited hangouts, distracting you and directing the information flows towards  less damaging routes. You are being managed. It makes me wonder if the UK Column is  run by military intelligence as Brian is ex-Navy and Alex is ex-MI6.

We truly are in the Matrix which were the last words spoken by the software CEO  Erin Valenti before she died on her way back from a meeting in Silicone valley (   A matrix of lies. You are not allowed to talk about bio-weapons and you are not allowed to talk about the corrupt networks running these operations. Here follows Dr Kevin McCairn’s video:

Dr Kevin McCairn exposes Interactive Internet Operation (57 mins)

A look at vaccine success (sic) in Iceland, the SC2 Viral Envelope and exposing the UK Column IIA (Interactive Internet Activities) operation. I have edited this down from 3.5 hrs but it still comes with a language warning.  He calls out and visits my website blog (Biblaridion at about 30 mins) during the live stream and plays the clip in my article “The UK Column in Denial”.


Here is the article on the SC2 envelope:

Mark from Housatonic was able to open a can of worms starting with Jewish CDC director Dr Rochelle Walensky.  This is what Kevin is referring to during the show when he mentions Auchincloss.  All the dots are beginning to join up.  Watch these two one minute videos:

Auchincloss part 1

Auchincloss part 2 – they got a CDC/NIAID/FDA coup


What does this mean?

It means the networks run deep and wide. It means they have captured everything.  Mark says the following:

Vanderbilt ancestors are running the CDC, FDA, AND NIAID. Sounds like a conflict of interest to me when one "discovers" the new pandemic virus, the other manages how to respond to it and develop the medicine, and the third part approves the medicine.
Research: 1) Dudleytown, Connecticut. 2) Dr. William Cogswell Clarke 3) Dark Entry Forest, Incorporated - Connect the dots. Flexner - Vanderbilt - Kennedy - Kissinger - Lederberg - Auchincloss - Skull and Bones - Medical experimentation - Memorial Sloan Kettering - Its getting real, folks. And now we know why Dr. Stephen Fauci's history was wiped. And now we get an idea of why Dr. Alice E. Moore got her home right next to Dudleytown, Connecticut ... and possibly why this area is heavily patrolled to keep people out.

Why does Fauci love the Spanish Flu so much? Note his deputy High Auchincloss' grandad created the tool used to drain the lungs of those people who died of it. Helpful if re-writing the narrative to be only caused by a "zoonotic" virus.

Why Fauci was picked - Because his deputy is Hugh Auchincloss. Family is married into Sloan. Powerful at Memorial Sloan-Kettering. And thats where Tony Fauci's dad Stephen Fauci was a pharmacist. Auchincloss is related to Bundy, Vanderbilt, Gore, Kennedy, and many more. An Auchincloss even replaced US Rep Joe Kennedy in Massachusetts. This is why Anthony Fauci was picked, and why he is immovable. Even worse - Auchincloss picked the CDC director Walensky, and Auchincloss relatives were FDA deputies. Meaning - control of finding pandemics, control of addressing pandemics, and control of approving the medicine. Holy holy crap. We got it. For those helping with the research, thank you - we all made this possible. Please share - please dammit share this.

The link in this tweet takes you to a connection map on LittleSis that will clarify many of the connections that go back to Sloan Kettering. This is based on the work done by Mark (Housatonic) and a click on the entery below each circle will take you to his research page:

Discord nukes Dr Kevin McCairn (18 mins)

Discord buys AI company Sentropy to shutdown free-speech under the guise of harassment and uses AI to nuke Dr Kevin M’cCairns server and all the associated user accounts. If you demonstrate from science that Covid is a bio-weapon and call out the nepotistic, corrupt institutions pushing forward communitarian wokeism (cultural Marxism) you get shut down.

In this video there is also a tweet about Amy Maxman sister of Isaac Maxman (part of the Maxwell-Epstein network) CEO of Predict getting the Cohen prize for writing (she attacked Kevin in the Nature Journal).  It is all one big corrupt swamp and they are all patting each other on the back and giving each other prizes.  But don’t you dare call them out because that would make you antisemitic.

Look what just came in over twitter….they are getting desperate to shut down any investigation into bio-weapons.

Gigaohm Biological 7th and 8th of Aug

Gigaohm Biological 7th and 8th of Aug

Wow, I have never seen J.C. so angry and disappointed (Aug 8th episode). He really lays into Sam Harris and tears him a new one.  These people refuse to discuss the biology…..they refuse.  They are bought and paid for.  Someone like J.C. or Kevin will never work in Academia again.  They burnt their bridges and put their money where their mouth is.  Respect.  It is good to find that there is still some integrity out there.  Some people who will stand up and do the right thing no matter the personal cost.

Slaves, and souls of men

Slaves, and Souls of Men

Extremely important – Please watch the video and read  the article and distribute


This next video by Jonathan Jay Couey  at Gigaohm Biological is one of his best and I will be distributing it widely.  It references numerous scientific articles and presents a powerful and well argued case.  You are probably as sick as me as hearing and reading about covid but it is extremely important that you understand the implications of the science.  I will place the links to the scientific articles (and the abstracts) underneath the video. 

What is happening now has spiritual and philosophical implications not just biological (health) implications.  I am going to discuss the penultimate article that he refers to in some depth and then offer a working hypothesis on what they are doing and what they are hoping to achieve. Please read the conclusion at the end.

The origin of the virus

The origin of the virus is key to understanding what is happening.   Was the virus man-made or was it a natural  virus (zoonotic) that jumped species?  We can emphatically state with confidence that it had a lab origin.  It was put together in a lab and can trigger numerous  inflammatory pathways……this is not normal:


In the center appears the SARS-CoV-2. Around it, at the upper part of the figure, appear autoantibodies linked to the SARS-CoV-2-infection. At the bottom part of the figure, appear autoimmune diseases linked to the SARS-CoV-2-infection [,, , , ,, , , , , , , , ].

For the moment we leave aside the question of who was involved but I want to point to a tweet from someone who is referred to by J.C. and who exposed what was happening very early on (like Jay did) – Harvard to the Big House:


Leaving aside the origins narrative I want to discuss the penultimate article that J.C. refers to as it is crucially important and rather frightening.

Imperfect Vaccination Can Enhance the Transmission of Highly Virulent Pathogens

The penultimate article that Jay discusses is about an experiment with vaccinated and unvaccinated chickens. Chickens carry a virus disease called Marek which probably originated because of the way they are farmed (so close together). Chickens become infected with Marek by inhalation of dust contaminated with virus shed from the feather follicles of infected birds.

In this experiment they put unvaccinated and vaccinated chickens together. The unvaccinated are birds are called by the fancy name immunologically-naïve sentinel birds.  My understanding is that they are a control group.  I got this definition on sentinels: “These immune system cells trawl through the epithelial tissues that serve as an interface between our bodies and the outside world: skin, lungs, intestines, etc. Known as the ‘sentinels’ of the organism, they capture all foreign or suspect molecules and carry them to the lymph nodes”.

So, I presume that sentinel is just a reference to the “feather follicles” etc that would form the first barrier (sentinel) to the virus. In other words a group of unvaccinated healthy birds with their immune system etc intact and naïve because it is still natural.  Now these sentinel birds come from the same commercial stock as the other birds  and so their mothers would have also been vaccinated with Rispens technically called CVI988/Rispens MDV (Marek Disease Vaccine) vaccine.  I have made my own diagram and placed a quote from the article underneath:


They used different vaccines during the test.  HPV= herpesvirus of turkeys.

MDV has been evolving in poultry immunized with leaky anti-disease vaccines since the  introduction of the first vaccines in 1970  All MD vaccines are live viruses administered to 18-day-old embryos or immediately after hatch, and vaccinated birds can become infected and shed wild-type virus . Wild-type MD viruses are so-called serotype 1 viruses. First-generation vaccines include a serotype 3 herpesvirus of turkeys called HVT; second-generation vaccines are a combination of HVT and SB-1, a serotype 2 isolate. Third-generation vaccines are based on an attenuated serotype-1 virus isolate CVI998, the so-called Rispens vaccine.

They also do experiments with Maternal derived antibody and conclude:

Our experiments above show that direct vaccination of birds or vaccination of parent hens makes possible the onward transmission of viral strains otherwise too lethal to transmit, and thus that unvaccinated individuals are put at increased risk of severe disease and death.

Making it far worse

So, Marek Viral Disease (MDV) is not eradicated by the vaccine.  The vaccine is not a sterilizing vaccine it is “leaky”  (does that sound familiar?).  It forces the pathogen to mutate and become more virulent. It keeps the shedding (vaccinated) chicken alive longer and so it can walk around and infect the unvaccinated.  In nature such a virus would kill the host and die out but because we invent a “vaccine” we are able to keep the chicken alive but turn the virus into something super lethal for the unvaccinated.  Geert vanden Bossche warned about this and we wrote an article about MDV months ago:

Ode to a Chicken


Gigaohm Biological 4th of July

I managed to download this one from Twitch so that I have a copy if it disappears.  Twitch only keeps the old live-streams up for 60 days.

Here follow all the links (resources) with the abstracts:

The spike protein of SARS-CoV-2 induces endothelial inflammation through integrin α5β1 and NF-κB


Vascular endothelial cells (EC) form a critical interface between blood and tissues that maintains whole-body homeostasis. In COVID-19, disruption of the EC barrier results in edema, vascular inflammation, and coagulation, the hallmarks of the severe disease. However, the mechanisms by which EC are dysregulated in COVID-19 are unclear. Here, we show that the spike protein of SARS-CoV-2 alone activates the EC inflammatory phenotype in a manner dependent on integrin α5β1 signaling. Incubation of human umbilical vein EC with whole spike, its receptor-binding domain, or the integrin-binding tripeptide RGD induced the nuclear translocation of NF-κB and enhanced the expression of leukocyte adhesion molecules VCAM1 and ICAM1, the adhesion of peripheral blood leukocytes, and the permeability of the monolayer. Inhibitors of integrin α5β1 activation prevented these effects. We suggest that the spike protein, through its RGD motif in the receptor-binding domain, binds to integrin α5β1 in EC to activate Rho GTPases, eNOS pathways, and the NF-κB gene expression program responsible for vascular leakage and leukocyte infiltration, respectively. These findings uncover a new direct action of SARS-CoV-2 on EC dysfunction and introduce integrin α5β1 as a promising target for treating vascular inflammation in COVID-19.


Vaccine-associated enhanced disease: Case definition and guidlines for data collection, and presentation of immunization data


This is a Brighton Collaboration Case Definition of the term “Vaccine Associated Enhanced Disease” to be utilized in the evaluation of adverse events following immunization. The Case Definition was developed by a group of experts convened by the Coalition for Epidemic Preparedness Innovations (CEPI) in the context of active development of vaccines for SARS-CoV-2 vaccines and other emerging pathogens. The case definition format of the Brighton Collaboration was followed to develop a consensus definition and defined levels of certainty, after an exhaustive review of the literature and expert consultation. The document underwent peer review by the Brighton Collaboration Network and by selected Expert Reviewers prior to submission.

Effectiveness of the BNT162b2 vaccine in preventing COVID-19 in the working age population – first results from a cohort study in Southern Sweden


Results The estimated vaccine effectiveness in preventing infection ≥7 days after second dose was 86% (95% CI 72-94%) but only 42% (95% CI 14-63%) ≥14 days after a single dose. No difference in vaccine effectiveness was observed between females and males. Having a prior positive test was associated with 91% (95% CI 85 to 94%) effectiveness against new infection among the unvaccinated.

Natural infection showed a 91% effectiveness against new infection. versus 86% effectiveness +7 days after second dose of BNT162B2 immunization.
Antibody response patterns in COVID-19 patients with different levels of disease severity in Japan  
We analyzed antibody response patterns according to the level of disease severity in patients with novel coronavirus disease 2019 (COVID-19) in Japan. We analyzed 611 serum specimens from 231 patients with COVID-19 (mild, 170; severe, 31; critical, 30). Immunoglobulin M (IgM) and IgG antibodies against nucleocapsid protein (N) and spike 1 protein (S1) were detected by enzyme-linked immunosorbent assays. The peaks of fitting curves for the optical density (OD) values of IgM and IgG antibodies against N appeared simultaneously, while those against S1 were delayed compared with N. The OD values of IgM against N and IgG against both N and S1 were significantly higher in the severe and critical cases than in the mild cases at 11 days after symptom onset. The seroconversion rates of IgG were higher than those of IgM against both N and S1 during the clinical course based on the optimal cut-off values defined in this study. The seroconversion rates of IgG and IgM against N and S1 were higher in the severe and critical cases than in the mild cases. Our findings show that a stronger antibody response occurred in COVID-19 patients with greater disease severity and there were low seroconversion rates of antibodies against N and S1 in the mild cases.
Kinetics of SARS-CoV-2 specific IgM and IgG responses in COVID-19 patients 
The emerging COVID-19 caused by SARS-CoV-2 infection poses severe challenges to global public health. Serum antibody testing is becoming one of the critical methods for the diagnosis of COVID-19 patients. We investigated IgM and IgG responses against SARS-CoV-2 nucleocapsid (N) and spike (S) protein after symptom onset in the intensive care unit (ICU) and non-ICU patients. 130 blood samples from 38 COVID-19 patients were collected. The levels of IgM and IgG specific to N and S protein were detected by ELISA. A series of blood samples were collected along the disease course from the same patient, including 11 ICU patients and 27 non-ICU patients for longitudinal analysis. N and S specific IgM and IgG (N-IgM, N-IgG, S-IgM, S-IgG) in non-ICU patients increased after symptom onset. N-IgM and S-IgM in some non-ICU patients reached a peak in the second week, while N-IgG and S-IgG continued to increase in the third week. The combined detection of N and S specific IgM and IgG could identify up to 75% of SARS-CoV-2 infected patients in the first week. S-IgG was significantly higher in non-ICU patients than in ICU patients in the third week. In contrast, N-IgG was significantly higher in ICU patients than in non-ICU patients. The increase of S-IgG positively correlated with the decrease of C-reactive protein (CRP) in non-ICU patients. N and S specific IgM and IgG increased gradually after symptom onset and can be used for detection of SARS-CoV-2 infection. Analysis of the dynamics of S-IgG may help to predict prognosis.
Kinetics of viral load and antibody response in relation to COVID-19 severity 

Abstract Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the causative agent for coronavirus 2019 (COVID-19) pneumonia. Little is known about the kinetics, tissue distribution, cross-reactivity, and neutralization antibody response in patients with COVID-19. Two groups of patients with RT-PCR–confirmed COVID-19 were enrolled in this study: 12 severely ill patients in intensive care units who needed mechanical ventilation and 11 mildly ill patients in isolation wards. Serial clinical samples were collected for laboratory detection. Results showed that most of the severely ill patients had viral shedding in a variety of tissues for 20–40 days after onset of disease (8/12, 66.7%), while the majority of mildly ill patients had viral shedding restricted to the respiratory tract and had no detectable virus RNA 10 days after onset (9/11, 81.8%). Mildly ill patients showed significantly lower IgM response compared with that of the severe group. IgG responses were detected in most patients in both the severe and mild groups at 9 days after onset, and remained at a high level throughout the study. Antibodies cross-reactive to SARS-CoV and SARS-CoV-2 were detected in patients with COVID-19 but not in patients with MERS. High levels of neutralizing antibodies were induced after about 10 days after onset in both severely and mildly ill patients which were higher in the severe group. SARS-CoV-2 pseudotype neutralization test and focus reduction neutralization test with authentic virus showed consistent results. Sera from patients with COVID-19 inhibited SARS-CoV-2 entry. Sera from convalescent patients with SARS or Middle East respiratory syndrome (MERS) did not. Anti–SARS-CoV-2 S and N IgG levels exhibited a moderate correlation with neutralization titers in patients’ plasma. This study improves our understanding of immune response in humans after SARS-CoV-2 infection.
T cell-mediated immune response to respiratory coronaviruses 


Emerging respiratory coronaviruses such as the severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome coronavirus (MERS-CoV) pose potential biological threats to humans. SARS and MERS are manifested as severe atypical pneumonia associated with high morbidity and mortality in humans. The majority of studies carried out in SARS-CoV-infected humans and animals attribute a dysregulated/exuberant innate response as a leading contributor to SARS-CoV-mediated pathology. A decade after the 2002–2003 SARS epidemic, we do not have any approved preventive or therapeutic agents available in case of re-emergence of SARS-CoV or other related viruses. A strong neutralizing antibody response generated against the spike (S) glycoprotein of SARS-CoV is completely protective in the susceptible host. However, neutralizing antibody titers and the memory B cell response are short lived in SARS-recovered patients and the antibody will target primary homologous strain. Interestingly, the acute phase of SARS in humans is associated with a severe reduction in the number of T cells in the blood. Surprisingly, only a limited number of studies have explored the role of the T cell-mediated adaptive immune response in respiratory coronavirus pathogenesis. In this review, we discuss the role of anti-virus CD4 and CD8 T cells during respiratory coronavirus infections with a special emphasis on emerging coronaviruses.


Mapping the human genetic architecture of COVID-19


The genetic makeup of an individual contributes to susceptibility and response to viral infection. While environmental, clinical and social factors play a role in exposure to SARS-CoV-2 and COVID-19 disease severity1,2, host genetics may also be important. Identifying host-specific genetic factors may reveal biological mechanisms of therapeutic relevance and clarify causal relationships of modifiable environmental risk factors for SARS-CoV-2 infection and outcomes. We formed a global network of researchers to investigate the role of human genetics in SARS-CoV-2 infection and COVID-19 severity. We describe the results of three genome-wide association meta-analyses comprised of up to 49,562 COVID-19 patients from 46 studies across 19 countries. We reported 13 genome-wide significant loci that are associated with SARS-CoV-2 infection or severe manifestations of COVID-19. Several of these loci correspond to previously documented associations to lung or autoimmune and inflammatory diseases3–7. They also represent potentially actionable mechanisms in response to infection. Mendelian Randomization analyses support a causal role for smoking and body mass index for severe COVID-19 although not for type II diabetes. The identification of novel host genetic factors associated with COVID-19, with unprecedented speed, was made possible by the community of human genetic researchers coming together to prioritize sharing of data, results, resources and analytical frameworks. This working model of international collaboration underscores what is possible for future genetic discoveries in emerging pandemics, or indeed for any complex human disease.
Virological and serological kinetics of SARS-CoV-2 Delta variant vaccine-breakthrough infections: a multi-center cohort study 


Objectives Highly effective vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have been developed but variants of concerns (VOCs) with mutations in the spike protein are worrisome, especially B.1.617.2 (Delta) which has rapidly spread across the world. We aim to study if vaccination alters virological and serological kinetics in breakthrough infections. Methods We conducted a multi-centre retrospective cohort study of patients in Singapore who had received a licensed mRNA vaccine and been admitted to hospital with B.1.617.2 SARS-CoV-2 infection. We compared the clinical features, virological and serological kinetics (anti-nucleocapsid, anti-spike and surrogate virus neutralization titres) between fully vaccinated and unvaccinated individuals. Results Of 218 individuals with B.1.617.2 infection, 84 had received a mRNA vaccine of which 71 were fully vaccinated, 130 were unvaccinated and 4 received a non-mRNA. Despite significantly older age in the vaccine breakthrough group, the odds of severe COVID-19 requiring oxygen supplementation was significantly lower following vaccination (adjusted odds ratio 0.07 95%CI: 0.015-0.335, p=0.001). PCR cycle threshold (Ct) values were similar between both vaccinated and unvaccinated groups at diagnosis, but viral loads decreased faster in vaccinated individuals. Early, robust boosting of anti-spike protein antibodies was observed in vaccinated patients, however, these titers were significantly lower against B.1.617.2 as compared with the wildtype vaccine strain. Conclusion The mRNA vaccines are highly effective at preventing symptomatic and severe COVID-19 associated with B.1.617.2 infection. Vaccination is associated with faster decline in viral RNA load and a robust serological response. Vaccination remains a key strategy for control of COVID-19 pandemic.
Imperfect Vaccination Can Enhance the Transmission of Highly Virulent Pathogens 


Could some vaccines drive the evolution of more virulent pathogens? Conventional wisdom is that natural selection will remove highly lethal pathogens if host death greatly reduces transmission. Vaccines that keep hosts alive but still allow transmission could thus allow very virulent strains to circulate in a population. Here we show experimentally that immunization of chickens against Marek's disease virus enhances the fitness of more virulent strains, making it possible for hyperpathogenic strains to transmit. Immunity elicited by direct vaccination or by maternal vaccination prolongs host survival but does not prevent infection, viral replication or transmission, thus extending the infectious periods of strains otherwise too lethal to persist. Our data show that anti-disease vaccines that do not prevent transmission can create conditions that promote the emergence of pathogen strains that cause more severe disease in unvaccinated hosts.


Monitor for COVID-19 vaccine resistance evolution during clinical trials  


Although less common than the evolution of antimicrobial drug resistance, vaccine resistance can and has evolved. How likely is it that COVID-19 vaccines currently in development will be undermined by viral evolution? We argue that this can be determined by repurposing samples that are already being collected as part of clinical trials. Such information would be useful for prioritizing investment among candidate vaccines and maximizing the potential long-term impact of COVID-19 vaccines.


One thing you should not do is vaccinate with a non-sterilizing “leaky” vaccine during a pandemic.  You should not vaccinate people that have no symptoms and you should especially not vaccinate kids.  If you do that you make the virus more virulent.  You make it worse.   That is exactly what they are doing.   Why are they doing it?  Are they stupid?  Of course not, they know exactly what they are doing.  They are destroying natural God given immunity and replacing it with a  needle.   This will give them the power of life and death at the end of a needle.  And because the “gene therapy” is patented they will literally own you.

You will own nothing but they will own you. According to Gordon Brown ex UK PM leaders at the G7 ‘will decide who lives and who dies, who is vaccinated and who is not’ 

Not only that but once they go fully digital on the block chain with the Central Banks they can regulate how and what you spend.  With AI and the surveillance  state they can make your digital tokens expire within a week.  You don’t spend it, and poof…. it is gone.   No such thing as saving.  You want to buy some fags and booze or pizza? Oops your digital cash does not work.  You want to run away from your digital prison? Oops your digital token refuses to work outside of a 5 km radius (and you are tracked anyway).  You said a naughty word about Zuckerburg…oops your social credit score tanks….no food for you tomorrow.

The future is full spectrum dominance of the “citizen”.  Your only escape will be death. They will control whether you live or breathe.

The title of this article comes from Rev 18 which describes the fall of Babylon the “Great city” she (The Great Harlot who rides the beast) committed fornication with the Kings of the earth and seduced them with her sorceries (pharmakeia). In her was found not only the wealth of the whole earth but the slaves and the souls (breath or life) of men. 

The Great Harlot has replaced God as the giver and taker  of life. She has dethroned God from his place among the cherubim (the living creatures representing the double helix wheels within wheels with the flashing Chatoyance (cats- eye Apatite ) phosphor backbone supporting the four bases (faces) of the living creatures (Ezekiel1).  She will make her supplicants trans-human. She owns it all and wants it all. Her hubris has reached to the heavens.


This is all planned.  They release a bio-weapon and then introduce a “vaccine”. Both Covid and the vaccine are dangerous.  Long-term the vaccine spike protein will activate neuro-degeneration or other inflammatory pathways.  That should weed out those with weak genetic dispositions.  The ones who survive will then be hooked on the needle.  Better be a good boy or girl because no jab and you are done. You will only have corporate immunity.  Any new disease and a vaccine will be rolled out.  What could possibly go wrong?  Ever wondered why God made us all different? Why nature likes variety vs mono-culture?  In the right circumstances people with a genetic defect might be the only ones to survive a pandemic.  These people are really very stupid.

This is your future if you keep vaccinating.  Stop vaccinating NOW.