{"id":238211,"date":"2023-01-06T20:09:52","date_gmt":"2023-01-06T19:09:52","guid":{"rendered":"https:\/\/climatescience.press\/?p=238211"},"modified":"2023-01-06T20:09:54","modified_gmt":"2023-01-06T19:09:54","slug":"how-covid-vaccines-cause-cancer","status":"publish","type":"post","link":"https:\/\/climatescience.press\/?p=238211","title":{"rendered":"How COVID Vaccines Cause Cancer"},"content":{"rendered":"\n
\"\"<\/figure>\n\n\n\n

<\/p>\n\n\n\n

From theepochtimes.com<\/a><\/p>\n\n\n\n

By Colleen Huber<\/a><\/p>\n\n\n\n

\"\"<\/figure>\n\n\n\n

(Africa Studio\/Shutterstock)<\/p>\n\n\n\n

<\/p>\n\n\n\n

Antibodies are studied more than other immune proteins for association with disease. This does not mean that they are more decisive in disease outcomes. Type I interferon likely has far more impact.<\/em><\/p>\n\n\n\n

<\/p>\n\n\n\n

Antibodies Are Not the Whole Story of Immune Resilience Toward Cancer<\/strong><\/h2>\n\n\n\n

Much is being made of a recent study showing IgG4 antibodies spiking in the blood labs of those who are triple-injected with the mRNA COVID vaccines.\u00a0\u00a0 Journalists are speculating that this may be the cause of increased cancers in the COVID-vaccinated.\u00a0 But that is not the main reason that the COVID-vaccinated are getting new cancer cases, sometimes aggressive \u201cturbo cancers,\u201d or coming out of remission from earlier cancer.\u00a0 <\/p>\n\n\n\n

Rather, there is earlier research that provides more plausible mechanisms for cancer risk, based on abundant prior knowledge of immune function.\u00a0 Let\u2019s look at both the new study on IgG antibodies and earlier research.<\/p>\n\n\n\n

The popular fallacy seems to be along these lines: \u2018Antibodies are easy to test for.\u00a0 Plus, they are the focus of vaccine development and vaccine action.\u00a0 So therefore we spend a lot of time thinking and talking about them.\u00a0 So therefore they must be important markers of disease outcomes.\u00a0 <\/p>\n\n\n\n

So therefore they must be decisive in disease outcomes.\u2019<\/p>\n\n\n\n

After focusing my own work on cancer patients for the last 16 years as a naturopathic oncologist, if I made this mistake in thinking, most of my patients would be dead by now from misdirected efforts.<\/p>\n\n\n\n

No, cancer remains a mega-problem of DNA damage, immune distraction, disrupted cell signaling, frenzied growth, lack of apoptosis, weakened tissues, angiogenesis, and metabolic derangement, as the principal features of an entity that feeds itself at the expense and to the detriment of the organ and the organism.\u00a0 <\/p>\n\n\n\n

These are the principal features of cancer, and they are hard as heck to treat successfully.\u00a0 I discuss that very daunting challenge\u00a0here<\/a>.<\/p>\n\n\n\n

<\/p>\n\n\n\n

IgG3 Versus IgG4<\/strong><\/h2>\n\n\n\n

First, let\u2019s look at the\u00a0new study on IgG3 versus IgG4 antibodies<\/a>\u00a0in the triple-jabbed.\u00a0 <\/p>\n\n\n\n

Herein, let\u2019s call it the IgG4 study.\u00a0\u00a0 It finds that the triple-jabbed may be developing a non-inflammatory tolerance to even high levels of spike proteins.\u00a0 <\/p>\n\n\n\n

That is, rather than having typical dyspnea, cough, olfactory and other full-blown COVID-type symptoms, IgG4 is a tolerant and tolerizing antibody that allows virions and spike protein load to accumulate in the body without the usual symptomatic alarms.\u00a0 Thus, a COVID+ PCR result with mild symptoms, or even no symptoms, often ensues.\u00a0 <\/p>\n\n\n\n

This may partly account for the many celebrities and politicians frequently quoted in MSM saying in so many words, \u2018I tested positive for COVID, but thanks to my shots, it\u2019s mild.\u2019 \u00a0\u00a0Yet their lack of effective immune defeat of SARS-CoV-2 is what prevents their developing a lasting neutralizing immunity.\u00a0 <\/p>\n\n\n\n

So they (at least at first) tolerate high spike protein loads and are perpetually vulnerable to recurrent infections. \u00a0\u00a0Even more worrisome, what underlies that recurrence of mild symptoms, show the IgG4 study authors, is a precarious derangement of immune function with potentially problematic stockpiling of viral load, spike proteins and antibodies, with potentially devastating consequences for their future health outcomes.\u00a0 <\/p>\n\n\n\n

Even a myeloma like abundance of immunoglobulins can create a\u00a0multiple myeloma-like disease<\/a>\u00a0in the COVID-vaccinated, a sludgy protein-laden blood that is harmful to the fine filtration structures, glomeruli, of the kidneys.<\/p>\n\n\n\n

That immune deviation, misdirection and derangement has been previously described as\u00a0pathogenic priming<\/em>, a maladaptation of the immune system to either ignore or to fight ineffectively against genuine threats, while at the same time focusing its resources to slay the paper tigers of non-threatening antigens.\u00a0 <\/p>\n\n\n\n

This happened in the design of the mRNA vaccines to produce a spike protein that was characteristic of the original Wuhan strain of SARS-CoV-2, but turned out to be ineffective against Delta, Omicron and subsequent strains, as some of us had earlier\u00a0warned<\/a>.\u00a0 <\/p>\n\n\n\n

Because the Wuhan strain had already flamed and burned out, the COVID vaccines were obsolete by the time they were offered to the public.<\/p>\n\n\n\n

Under circumstances of natural infection, whereas IgM antibodies flare for a short time after infection onset, IgG antibodies, in contrast, are slower to develop, and are those that remain long after an infection has resolved.  (For example, my measles IgGs are still robust on a blood lab decades after I had measles as a child, with only natural immunity, no vaccine history.)<\/p>\n\n\n\n

The subclass IgG4 is a non-inflammatory one that is correlated with tolerance to antigens, similar to allergy shots rendering the immune response more tolerant to grass pollen. \u00a0\u00a0<\/p>\n\n\n\n

IgG4 has no known effector function.\u00a0 Likewise, IgG4 seems to be inversely correlated with anaphylaxis.\u00a0 \u00a0<\/p>\n\n\n\n

Here, in the IgG4 paper, regarding the COVID-vaccinated, IgG4 increases considerably, over 38 times, after a third mRNA injection.\u00a0 Please note that the scale of the y-axis is logarithmic, putting the IgG4s quite far up there.<\/p>\n\n\n\n

\"\"<\/figure>\n\n\n\n

At the same time, both triple- and double-jabbed lose a considerable amount of their IgG3 antibodies, discovered at 180-day and 210-day follow-up labs, respectively.\u00a0 Note again the logarithmic scale, showing cratering drop-off of IgG3 antibodies, with skyrocketing IgG4 antibodies.\u00a0\u00a0 This is from Figure 1 of the\u00a0IgG4 paper<\/a>:<\/p>\n\n\n\n

\"\"<\/figure>\n\n\n\n

The subclass IgG3 is sometimes thought, including by the IgG4 authors, to be pro-inflammatory, one of many immune assaults against invading pathogens.  Although there is evidence to the contrary<\/a> as well.  IgG3 is thus sometimes assumed, including by the IgG4 authors, and interested journalists, to neutralize, or fight effectively against, antigens.<\/p>\n\n\n\n

However, there is little support, other than correlation of titers, for the assertion that IgG3 antibodies may be effective warriors against pathogens.  The IgG4 study authors acknowledge an earlier observation of \u201cIgG3 responses correlating with partial protection against HIV<\/a>,\u201d and only a rise in IgG3 antibodies after natural infection with SARS-CoV-2, such as reported here<\/a>, without mechanism of its protection.<\/p>\n\n\n\n

One possible clue as to the IgG4 study authors\u2019 observations of low IgG3 is the glycosylation of IgG3<\/a> as impactful on SARS-CoV-2 infection severity.  (Immunoglobulins are glycosylated protein molecules generally, but hyper-glycosylation seems to be a problem.  Glycosylation is generally detrimental to its optimal function; notorious glycosylation has devastated more than simply antibodies, in our junk food loving culture.)<\/p>\n\n\n\n

IgG3 antibodies are a very small proportion of IgG antibodies and have not yet been well-studied<\/a>.  Both IgG3 and IgG4 antibodies are generally a small proportion of all our B-cells, 3% and 4% respectively.<\/p>\n\n\n\n

Low IgG3 antibodies are not necessarily correlated with low disease severity.\u00a0 For example, in COPD, we see\u00a0this correlation<\/a>\u00a0of\u00a0low<\/strong><\/em>\u00a0IgG3 levels with life-threatening exacerbations of COPD.\u00a0 All antibodies,\u00a0including IgG3 and IgG4<\/a>, generally rise and then fall in case of natural infection.\u00a0 Below I will explain why I am not so sure the cause and effect vector goes as is currently being assumed, from low IgG3 \/ IgG4 ratio to generalized immune dysfunction.\u00a0 Rather, I suspect that it may more likely be an effect of other mechanisms, described below.<\/p>\n\n\n\n

<\/p>\n\n\n\n

There Is so Much More to Immune Function Than Only Antibodies<\/strong><\/h2>\n\n\n\n

The first problem with the current IgG fascination is the assumption that just because antibodies consume much attention, and are easily measurable proteins on a blood lab, that they are then necessarily impactful on the vast complexity of the rest of the immune system.\u00a0 <\/p>\n\n\n\n

Metaphorically, by assuming that that which we can see is necessarily decisive, we are looking at the skin, so to speak, and assuming that we therefore know the functions of the internal organs and that the skin is the dominant cause of internal effects.\u00a0 Obviously, such is not the case.<\/p>\n\n\n\n

Let\u2019s first assume that the highly mobile and ubiquitous blood contains many of the cells in our immune system and are, as a whole and in parts, key to optimal immune function.  Here is the proportion of IgG immunoglobulin antibodies to the rest of the immune system:<\/p>\n\n\n\n

Immunoglobulins are present on the surface of B-cells, where they act as receptors for antigens.  B-cells fluctuate in number, but average 5.2% of all white blood cells.  White blood cells are 0.1% of all cells in the blood.  Therefore B-cells are about 0.00005% or 5 in 100,000 cells in the blood.<\/p>\n\n\n\n

I explain further about that\u00a0here<\/a>.<\/p>\n\n\n\n

\"\"<\/figure>\n\n\n\n

This proportion of B-cells to other cells in the blood is vanishingly small.\u00a0 If you can see the very skinny red line at the far left of the band below, that is the proportion of all B-cells compared to the vast remainder of cells in the blood.\u00a0 (The thin red line would actually need to be a little thinner to be true to scale.)<\/p>\n\n\n\n

Now let\u2019s look at other aspects of immune function that are powerhouse fighters against cancer, but have been associated with high viral load and\/or high spike protein, such as is expected to occur after COVID vaccination.  These researchers found that two of our most important cancer-fighting cells, natural killer (NK) cells and CD8+ T-cells were significantly reduced<\/a> in these circumstances.  Reduction in NK cells is seen with more aggressive tumors.<\/p>\n\n\n\n

But the major problem with the mRNA COVID vaccines and cancer risk was shown in April of this year, in the Seneff, Nigh paper<\/a>.<\/p>\n\n\n\n

The science community\u2019s pre-occupation with the relatively smaller adaptive immune system, mostly its humoral portion, and unfamiliarity or disinterest in the vastly more important and stronger innate immune system has led attention away from this seminal paper.\u00a0 \u00a0<\/p>\n\n\n\n

I have to recommend not only reading but thoroughly studying the Seneff, Nigh paper for the best understanding to date of the effect of the COVID vaccines on tumorigenesis, immune-failure with respect to cancer and metastatic events.<\/p>\n\n\n\n

What Seneff et al found is that the most profound threat to immune function by the mRNA vaccines is the interference with Type I interferon signaling pathways.\u00a0 <\/p>\n\n\n\n

This in turn debilitates the surveillance capabilities of the immune system in cancer detection.\u00a0 As a result, we see both new tumors and metastases of existing cancers in the COVID-vaccinated.\u00a0 <\/p>\n\n\n\n

We see what is now called turbo cancers.\u00a0 Here is how Seneff et al supports that hypothesis.\u00a0 Their paper is enormously detailed, and my summary of it below is quite brief.<\/p>\n\n\n\n

Ivanova, et al<\/a>\u00a0found that people who were naturally infected with SARS-CoV-2 have been able to dramatically up-regulate our arguably most crucial cytokine, Type I interferon, as seen from their peripheral dendritic cells, whereas mRNA-vaccinated people have not shown this ability, nor any such increase, nor any progenitor cells for the same.\u00a0 <\/p>\n\n\n\n

From those various findings, is evident that the COVID vaccines suppress Type I interferon signaling.\u00a0 <\/p>\n\n\n\n

The results are a devastating breakdown of many downstream immune functions, creating new vulnerability to not only viral diseases, but also to cancer. The necessity of interferons for the body\u2019s war against cancer is further seen in the productive clinical use over decades of interferon as a therapeutic agent to cancer patients.<\/p>\n\n\n\n

The most appreciated mechanisms of Type I interferon against cancers include up-regulation of the tumor suppressor gene p53, as well as kinase inhibitors, and the resulting arrest of cancer\u2019s cell reproduction.\u00a0 <\/p>\n\n\n\n

Perhaps even more crucial is that Interferon-alpha, a type of interferon I,\u00a0makes cancer recognizable<\/a>, or in a way visible to other immune cells for destruction.\u00a0 Two other major effects of Type I interferons, specifically interferon-alpha, are cell differentiation and apoptosis, which are two of the major events that are important for a natural victory over cancer.\u00a0 Type I interferon also activates the essential cancer-fighting cells discussed above, CD8+ and NK cells.\u00a0 <\/p>\n\n\n\n

There are further genetic effects of Type I interferons, each of which tend to suppress tumors, notably through\u00a0IRF-7 genes<\/a>.\u00a0 These genes have impact on\u00a0cancers<\/a>\u00a0of the breast, prostate, uterus, ovaries and pancreas.\u00a0 But these and oncogenes generally appear to become dysregulated by the mRNA vaccines.<\/p>\n\n\n\n

Fay et al<\/a>\u00a0discuss G-quadruplex formations in RNA, and that role in proto-oncogene expression.\u00a0 This can in turn lead to cancer progression.<\/p>\n\n\n\n

<\/p>\n\n\n\n

Cancer Incidence<\/strong><\/h2>\n\n\n\n

Even before the boosters were rolled out to the public, the Vaccine Adverse Events Reporting System (VAERS) of the Dept of Health and Human Services (HHS) showed vastly more cancers following COVID vaccines than for all other vaccines during the 30-year history of VAERS.\u00a0 These new cancers following the COVID vaccines accounted for 98% of cancers reported.\u00a0 Here again from Seneff et al:<\/p>\n\n\n\n

\"\"<\/figure>\n\n\n\n

Seneff, Nigh et al\u00a0https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC9012513\/<\/a><\/p>\n\n\n\n

<\/p>\n\n\n\n

It should be noted that the reporting of these 2021 cancers occurred in large part prior to the US public\u2019s (tepid) uptake of even the earliest mRNA COVID boosters (injection #3 in the fall of 2021) as here shown in\u00a0Our World in Data<\/a>.<\/p>\n\n\n\n

\"\"<\/figure>\n\n\n\n

That 3rd injection is the one after which the IgG4 paper authors saw the most difference in IgG3\/IgG4 ratios, but not necessarily the greatest increase in cases of cancer.<\/p>\n\n\n\n

Let\u2019s consider the whole immune system, not only immunoglobulins, as necessary to protect against the ravages of cancer.  Immune cells and cytokines, and their exquisitely coordinated and synergistic functions, must be protected from the destructive events initiated by irreversible experimental injections of novel products, such as the mRNA vaccines.<\/p>\n\n\n\n

Reposted from the author\u2019s\u00a0Substack<\/a><\/em><\/p>\n\n\n

\n
\"Colleen<\/a><\/figure>\n<\/div>\n\n\n

Colleen Huber<\/a><\/p>\n\n\n\n

Author, The Defeat Of COVID, Manifesto for a Cancer Patient, and Choose Your Foods Like Your Life Depends On Them, all on Amazon. <\/p>\n\n\n\n

Naturopathic Medical Doctor (NMD) x 15 years.<\/p>\n","protected":false},"excerpt":{"rendered":"

Let\u2019s first assume that the highly mobile and ubiquitous blood contains many of the cells in our immune system and are, as a whole and in parts, key to optimal immune function.<\/p>\n","protected":false},"author":121246920,"featured_media":238228,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_coblocks_attr":"","_coblocks_dimensions":"","_coblocks_responsive_height":"","_coblocks_accordion_ie_support":"","advanced_seo_description":"","jetpack_seo_html_title":"","jetpack_seo_noindex":false,"jetpack_seo_schema_type":"","_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_wpcom_ai_launchpad_first_post":false,"_jetpack_hide_featured_image":false,"_jetpack_featured_image_duplicate_dismissed":0,"_jetpack_feature_clip_id":0,"_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":true,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2},"jetpack_post_was_ever_published":false},"categories":[1],"tags":[],"class_list":["post-238211","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-uncategorized"],"jetpack_publicize_connections":[],"jetpack_likes_enabled":true,"jetpack_shortlink":"https:\/\/wp.me\/paxLW1-ZY7","jetpack-related-posts":[{"id":245208,"url":"https:\/\/climatescience.press\/?p=245208","url_meta":{"origin":238211,"position":0},"title":"18 months too late: natural immunity is *almost* as good as vaccination (except when it\u2019s better)","author":"uwe.roland.gross","date":"02\/23\/2023","format":false,"excerpt":"They found the reinfection rate of people who caught Covid was lower than people who were given Pfizer or Moderna.","rel":"","context":"Similar post","block_context":{"text":"Similar post","link":""},"img":{"alt_text":"","src":"https:\/\/i0.wp.com\/climatescience.press\/wp-content\/uploads\/2023\/02\/image-693.png?fit=1080%2C675&ssl=1&resize=350%2C200","width":350,"height":200,"srcset":"https:\/\/i0.wp.com\/climatescience.press\/wp-content\/uploads\/2023\/02\/image-693.png?fit=1080%2C675&ssl=1&resize=350%2C200 1x, https:\/\/i0.wp.com\/climatescience.press\/wp-content\/uploads\/2023\/02\/image-693.png?fit=1080%2C675&ssl=1&resize=525%2C300 1.5x, https:\/\/i0.wp.com\/climatescience.press\/wp-content\/uploads\/2023\/02\/image-693.png?fit=1080%2C675&ssl=1&resize=700%2C400 2x, https:\/\/i0.wp.com\/climatescience.press\/wp-content\/uploads\/2023\/02\/image-693.png?fit=1080%2C675&ssl=1&resize=1050%2C600 3x"},"classes":[]},{"id":240902,"url":"https:\/\/climatescience.press\/?p=240902","url_meta":{"origin":238211,"position":1},"title":"New Study: COVID Vaccines \u2018Profoundly Impair\u2019 Protective Immunity, \u2018Probably Enhance Disease Severity\u2019","author":"uwe.roland.gross","date":"01\/21\/2023","format":false,"excerpt":"Recipients of repeated COVID-19 mRNA vaccinations may have fully damaged their immune system\u2019s capacity to protect them from severe effects from the disease. 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September 2023 Unusually aggressive cancers in children and people in their 20s and s 30s\u2026possible damaged immune system cancer surveillance\u2026\u00a0 Truly, I\u2019m really glad I stood my ground and resisted getting sucked into taking what we today know was a risky, untested, slipshod experimental medicine. 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