The results of this report has been highlighted recently by the ITV News reporter, Robert Peston<\/a> who despite being double-vaccinated became ill with COVID. He wanted to know how common his experience was, and he was shocked by what he found. He says, \u201cI am surprised these statistics have received so little attention and have occasioned so little debate.\u201d<\/p>\n\n\n\n According to the latest government official UK reports<\/a>, case rates per 100,000 are now double in the double vaccinated population<\/a> compared to the unvaccinated for people aged 40 to 79. Apart from anything else, these data would appear to throw any argument for having vaccine passports well and truly into the sin bin.<\/p>\n\n\n\n Furthermore, a review of COVID immunity studies published by Brownstone<\/a> asks how effective is immunity after COVID recovery relative to vaccination? This follows an Israeli study<\/a> that found that the vaccinated have a 27 times higher risk of symptomatic infection than the COVID recovered. The study also found that the vaccinated were nine times more likely to be hospitalised for COVID. On the other hand, a CDC study<\/a> claims that patients who have recovered from COVID are five times more likely to be hospitalised for COVID than the vaccinated.<\/p>\n\n\n\n As the Dr Martin Kulldorff<\/a> points out, “Both studies cannot be right”. <\/p>\n\n\n\n There are a number of peer-reviewed publications now providing reasons why mRNA vaccination could potentially cause an increased risk of COVID infection, or have other risks:<\/p>\n\n\n\n 1. The well reported drop in white cell count<\/a> (neutrophyls) immediately following vaccination.<\/p>\n\n\n\n 2. Immune focus on a single antigen (spike protein) and associated variant selection<\/a> causes vaccine break-through. The explosion in the number of new variants following vaccination is being monitored by the international collaboration of scientists, Nextstrain<\/a>. There are millions of complete SARS-CoV-2 genomes available and this number increases every day.<\/p>\n\n\n\n 3. Antibody dependent enhancement; anti-SARS-CoV-2 antibodies could actually exacerbate COVID-19 through antibody-dependent enhancement<\/a> (ADE). ADE is a reminder that not all antibody responses are helpful and some can be harmful.<\/p>\n\n\n\n 4. Vaccine induced auto-immune responses including VITT. As reported by JAMA Neurology<\/em><\/a>, circulating platelet-activating platelet factor 4 (PF4) antibodies have been found in many patients suffering from vaccine-induced immune thrombotic thrombocytopenia (VITT). This is probably caused by injection components binding with the person’s own platelet factor to create a ‘neo-antigen’. This neo-antigen is what then causes an immune response resulting in clotting, intracerebral haemorrhage and the death of around half of those people affected.<\/p>\n\n\n\n 5. Natural immunity provides better protection; there is increasingly overwhelming evidence<\/a> that natural immunity is more powerful and broader in terms of preventing infection. The largest study<\/a> yet comparing COVID vaccines to natural infection has produced results that would have surprised no one 50 years ago.<\/p>\n\n\n\n 6. A jab in the arm can’t work. According to the Journal of Immunology,<\/em><\/a> “The route of vaccination is important in influencing immune responses at the initial site of pathogen invasion where protection is most effective”. Molecular immunologist, Professor Edward Steele<\/a> points out that a jab in the arm cannot protect against a mucosal viral invasion<\/a> – purely on the basis of first principles. It is an antibody known as IgA predominantly found in our nasal, lung and gut mucosa that is responsible for the first line of defence<\/a> against respiratory infections. Unless the IgA is activated the vaccine simply can’t work. This observation would seem to demonstrate a fairly fundamental flaw in the inoculation method.<\/p>\n\n\n\n 7. Vitamin D deficiency; T-cells can only fight viral infections when there is sufficient vitamin D present. When a T-cell is exposed to a pathogen such as a virus, it extends a signalling device or ‘antenna’ known as a vitamin D receptor<\/a>, with which it searches for vitamin D<\/a><\/p>\n\n\n\n 8. The spike protein may itself toxic and prevent DNA repair; a recent study<\/a> that looked at what actually happened to the spike protein has demonstrated a potential molecular mechanism by which the spike protein might impede adaptive immunity and underscore the potential side effects of full-length spike-based vaccines. The spike protein appears to localise in the nucleus, and here it inhibits DNA damage repair by impeding key processes.<\/p>\n\n\n\n 9. According to the Journal of Immunology<\/em> Original Antigenic Sin<\/a>, or OAS.<\/p>\n\n\n\n The body’s immune system can normally recognise foreign infectious material from the types of structures displayed. These structures that can cause an immune response – such as the production of antibodies are known as antigens.<\/p>\n\n\n\n The virus ‘variants’ vary because they have slightly different or modified antigenic structures around their surfaces. Evolution will normally select for those viruses with antigenic structures that evade or are not recognised by the immune system.<\/p>\n\n\n\n The first (original) exposure of the immune system to an antigen (or the ‘pioneer’ strain) is critical for how immunity will subsequently develop, and the composition of the antibody repertoire (i.e. the quality of your defence mechanisms). The more surface antigens that the immune system responds to, the more ‘memory’ the immune system will have for dealing with subsequent infections. <\/p>\n\n\n\n So, there is a real concern that a narrow-spectrum vaccine with suboptimal antibodies that only recognise the spike protein of the virus and not the “N” or nucleocapsid part of the virus will interfere or trip up the natural immune response. The spike protein will cause B cells in those with the vaccine to learn to produce only spike protein antibodies. These antibodies are slower-acting and less sterilising than the N antibodies, which are faster and more effective.<\/p>\n\n\n\n The opening lines of the famous ‘Essential Immunology’ 3rd Edition – (see pic NB the cartoons are not original textbook artwork, but have been applied by appreciative students), by Professor Ivan Roitt state, \u201cMemory, specificity and recognition of \u2018non-self\u2019 \u2013 these lie at the heart of immunology. Our experience of the subsequent protection (immunity) afforded by exposure to many infectious illnesses can in fact lead us to this view\u201d. <\/p>\n\n\n\n Pretty much all the evidence points at this statement being particularly true. However, the nature of that first immune priming could be critical. A sub-standard prime can cause the concept of \u2018original antigenic sin\u2019.<\/p>\n\n\n\n This biological phenomenon could be problematic for a vaccine with only a single (spike protein) antigen.<\/p>\n\n\n\n If memory B cells (the cells responsible for producing antibodies) respond to an infection with a related, but antigenically distant pathogen, the memory response can not only be ineffective but possibly diminish the effectiveness of naive B cells capable of producing neutralising antibodies. It is understood that this potential downside of immune memory must be considered when attempting to design vaccines incase a vaccine formulation induces an immunological setback that prevents protective immunity<\/a> to a new strain of virus.<\/p>\n\n\n\n So, if OAS plays such an important function in preventing subsequent infections, the nature of the first (original) antigenic stimulus (or vaccine) is potentially a fundamental factor for preventing subsequent infections. the vaccine may produce an initial immune response, but OAS then suppresses subsequent responses to variants.<\/p>\n\n\n\n NB OAS in this sense should not be confused with the other OAS1, or oligoadenylate synthase 1 which, is a type of protein. However, OAS1 (the protein) and associated genes, have also been demonstrated to play an important role in our natural defence<\/a> against RNA viruses. From an evolutionary perspective, what is even more interesting is that the type of OAS1 that lends the greatest protection is associated with Neanderthal man<\/a>.<\/p>\n\n\n\n As reported in the journal Nature<\/em><\/a>; measuring OAS1 levels found that higher plasma OAS1 levels in a non-infectious state were associated with reduced COVID-19 susceptibility and severity. Further analyses suggested that a Neanderthal isoform of OAS1 in individuals of European ancestry affords this protection. Thus, evidence supports a protective role for OAS1 in COVID-19 adverse outcomes. Available pharmacological agents that increase OAS1 levels could be prioritized for drug development.<\/p>\n\n\n\n Furthermore, when comparing population statistics such as ‘case’ rates or treatment or vaccine outcomes, the relative prevalence of OAS1 in the groups should be included in order to help ensure fair comparisons. Otherwise, the risk is that those groups with higher Neanderthal ancestry will appear to have responded better.<\/p>\n\n\n\n Returning to OAS in the sense of ‘original antigenic sin’, and looking at the work required to create effective vaccines against viruses without risk of inducing ‘sin’, the 2019 Journal of Immunology<\/em> paper concludes stating:<\/p>\n\n\n\n Recently, there has been a major expansion in research and funding dedicated to the development of better and more broadly protective influenza virus vaccines. This, in turn, has catalyzed substantial renewed interest in defining the mechanisms governing OAS and the influence that pre-existing immunity exerts on subsequent vaccine responses. Although many specific instances wherein OAS-like responses have been observed, both experimentally and during natural influenza virus epidemics, have been studied in great detail, a holistic and predictive model of the situations in which OAS responses occur is far from being realized. To accomplish this goal, considerable effort will need to be directed to understanding the complex interactions between Abs, cell types, and Ags that ultimately determine response outcomes.<\/p>\n\n\n\n Abs = antibodies<\/p>\n\n\n\n Ags = antigens<\/p>\n\n\n\n So, the better the vaccine, the fewer the number of boosters required. There is also a question over whether increasing the number of boosters with what is already a sub-quality ‘immune prime’ compared to a natural infection, may actually have the reverse effect to the one intended.<\/p>\n","protected":false},"excerpt":{"rendered":" Updated Wednesday, November 3, 2021 – 19:53Published Sun, 09\/12\/2021 – 21:39 The latest Public Health England reports are showing that in some age groups the rates of COVID infection are higher in vaccinated patients than unvaccinated. … Leer m\u00e1s<\/a><\/p>\nReasons why COVID vaccines may not work<\/h3>\n\n\n\n
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<\/figure>\n\n\n\nWhat is original antigenic sin?<\/h3>\n\n\n\n
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<\/figure>\n\n\n\nNatural immunity v. mRNA vaccines<\/h3>\n\n\n\n
Neanderthal ancestry may provide greater protection<\/h3>\n\n\n\n
The risk of induced ‘sin’<\/h3>\n\n\n\n
More boosters?<\/h3>\n\n\n\n