Please Don’t Call Me A Visionary! Geert Vanden Bossche on the impact of mounting population level immune pressure on COVID virus infectious pressure; Africa has won!

we underestimated and discounted the evolutionary dynamics and complex interplay between population immune pressure and circulating viral infectious pressure, bi-directional

Start Geert here:

‘My warnings about the bleak outcome of this pandemic — which started as a natural event but was turned into a massive in vivo gain-of-function experiment by human intervention — have mostly been met with scorn. Many people think I’m an idiot or a conspiracy theorist. But honestly, I don’t let it get to me too much. I understand that if you haven’t really dug into the complex dynamics of this immune escape pandemic, it’s almost impossible to see that my predictions are actually based on rational, scientific reasoning.

On the flip side, those with whom I feel aligned in terms of mindset and aware of the damage caused by this large-scale interference in population immunity often call me a “visionary”. They seem amazed by how easily they think I can “see the future.” That label, though, because calling it “visionary” kind of downplays all the years of scientific insights, careful reasoning, and hard-earned knowledge behind it.

Voice for Science and Solidarity by Geert Vanden Bossche is a reader-supported publication. To receive new posts and support my work, consider becoming a free or paid subscriber.

Subscribe

In the past, I used to write (too) long articles, hoping that at least my peers or public health authorities would understand my reasoning — maybe even challenge it. Now, I try to keep things more concise. And this is my final attempt to clearly and as briefly as possible explain where we’re heading in this ongoing pandemic, and why the current developments — even though they can’t be reversed — are unfolding painfully slowly, yet certainly. These days, ChatGPT is a huge help when it comes to explaining concepts or terms people might not be familiar with or breaking down scientific jargon, I sometimes assume you already understand. So please feel free to check with ChatGPT whenever you feel like I’m skipping steps or making things too dense. Below, I’ve highlighted in bold the terms that you can easily have ChatGPT define and explain.
I honestly don’t understand why evolutionary biologists still haven’t acknowledged the crystal-clear case of SARS-CoV-2 (SC-2) adapting under population-level immune pressure as a textbook example of one of the fields they’re supposed to study, i.e., evolutionary ecology! Most of them have stayed surprisingly quiet about the catastrophic impact of the large-scale COVID-19 (C-19) vaccination campaign, despite its huge impact on the dynamics of SC-2 evolution and the host adaptive immune response. The only conclusion I can draw is that they lack the necessary background in virology, immunology, and vaccinology to fully grasp how the immunological landscape in a highly C-19 vaccinated population affects viral evolutionary dynamics.

About entropy, resilience and chaos…

As a bit of context, I’d first like to point out how this pandemic fits perfectly into today’s broader pattern of entropic, disorder-related events occurring across almost all layers of industrialized societies. To name just a few: disruption, disintegration, discontinuity, disharmony, distortion, displacement, dissonance, distrust, dissent, dysregulation, dysfunction, dystopia, destruction, degeneration, deterioration, degradation, destabilization, decoupling...

However, disturbances in natural balance don’t necessarily transition into full-blown chaos or system breakdown. Still, without mechanisms for adaptation or resilience, there’s a very real risk that systems collapse — suddenly and irreversibly. Where it is currently most obvious—at least to me—that we are running out of the ability to adapt or remain resilient is in the ongoing immune escape pandemic: after 5–6 years of increasingly disruptive influences — mainly irrational infection-control measures followed by poorly thought-out mass vaccination — the population’s immunity has largely lost its ability to effectively adapt to continued viral immune escape. Once the elastic is stretched to its limit, there may be no more tension left (hence the current decline in case numbers and viral spread), but any further traction meets a total lack of resilience — and the elastic just snaps very suddenly! Given the current situation and the absence of protective herd immunity, and thus the lack of control over virus transmission, we have no choice but to let the pandemic run its course. It’s just a matter of time before the elastic will snap… and probably not much. I still believe that in this high-entropy phase of modern civilization, further viral evolution in highly C-19 vaccinated populations is the most likely factor to trigger societal collapse. This non-linear collapse would likely prevent the breakdown of other already-strained systems. This might be the only positive element in an otherwise bleak scenario.

The evolutionary pathobiology of SC-2: It’s not a never-ending story!

In the context of the currently diminished adaptive immune pressure exerted by highly C-19 vaccinated populations, the (co-)dominance of viral variants is no longer primarily driven by immune escape. Poorly selective immune pressure—e.g., resulting from low-affinity, poorly epitope-specific antibodies and suboptimally functional T cells—slows down viral immune escape, as it fails to strongly favor specific viral variants capable of evading the host immune response. Consequently, newly emerging immune escape variants of SC-2 no longer exhibit a significant competitive fitness advantage, as they do not replicate substantially better than circulating variants. In addition, the broadening of population-level immune pressure requires the virus to accumulate multiple epitope mutations simultaneously to effectively escape host immunity. The generation of such immune escape variants is therefore likely to require more time, particularly in view of the reduced replication advantage and potential fitness costs associated with these accumulated mutations.

In the absence of significant immune selection pressure, variants with higher intrinsic infectiousness may leverage this fitness advantage to dominate via purifying selection, thereby tending to genetically stabilize the SC-2 landscape by purging immune escape variants that carry a fitness cost due to harmful mutations. However, given the immune-mediated reduction in viral load shed by the reservoir of chronically SC-2 infected individuals—reflected by low wastewater viral RNA levels—combined with rising summer temperatures, it is reasonable to assume that highly C-19-vaccinated population are increasingly facing a transmission bottleneck, despite the enhanced replicative fitness of newly emerging variants. This may explain why viral variants currently increasing in prevalence have integrated mutations that interfere with the host’s innate antiviral defenses, thereby amplifying viral load and shedding, and enhancing their transmissibility. Although such additional mutations may, in turn, compromise viral fitness, variants carrying them may exploit this transient transmission advantage before being eliminated through purifying selection. This is particularly relevant when considering large bottlenecked or chronically SC-2-infected populations, such as highly C-19–vaccinated cohorts.
Provided that a newly emerging variant replicates at sufficiently high titers and harbors 'tolerable' mutations that impair the host’s innate antiviral immunity—such as those inhibiting or suppressing type I interferon (IFN) induction (https://x.com/mrmickme2/status/1927515038098620651)—the mutation sampling effect may become strong enough to allow the virus to exploit a narrow window of opportunity to overcome the transmission bottleneck. Under such conditions, even atypical or seemingly disadvantageous mutations can be positively selected, despite the absence of genuine adaptive immune selection pressure.
The narrowing of the immune-mediated SC-2 transmission bottleneck by high environmental temperatures may already explain why the NB.1.8.1 variant is currently on the rise in Southeast Asia, leading to a surge in infections and increased hospitalizations among vulnerable individuals. This illustrates that even immune escape variants bearing rare mutations with an intrinsic fitness cost can dominate if they confer a sufficient transmission advantage—for instance, by weakening or impairing additional key components of the host’s innate immune defense. This enables faster intra-host replication in chronically SC-2-infected individuals and more efficient inter-host transmission, allowing such variants to outcompete all other intra-host strains and rapidly rise to dominance in the population.

The dominance of highly infectious and more transmissible variants, as described above, may also explain why infections with the currently circulating strains provoke more pronounced localized viral replication in the upper respiratory tract (URT), often resulting in severe throat inflammation—commonly referred to as ‘razor blade throat.’

However, as extensively referenced in my online courses, strong inflammatory signals triggered by enhanced viral replication in the URT upregulate lectin expression on the surface of URT-patrolling migratory dendritic cells (DCs), which in turn reduces the replicative fitness of the transmitted virus. There is little doubt that this innate, DC-mediated antiviral mechanism will be countered by the emergence of new variants that not only benefit from the aforementioned transmission advantage but also incorporate additional mutations that suppress infection-inhibiting innate immunoinflammatory signaling—e.g., through modulation of pattern recognition receptors (PRRs), co-stimulatory molecules, or pro-inflammatory cytokine responses—that would normally be triggered by productive viral infection, or that alternatively modify the viral glycosylation profile to prevent effective binding of viral glycans to DC-associated lectins.
Even if such additional mutations compromise viral viability, some of these newly emerging immune escape variants may evade purifying selection by achieving transmission before being eliminated, as explained above. Hence, such newly emerging variants would effectively use currently (co-)circulating variants—such as NB.1.8.1—as a stepping stone for further adaptive evolution, enabling the virus to further undermine the maladaptive immune response that meanwhile prevails in large segments of highly C-19 vaccinated populations.

If a highly infectious circulating variant acquires such a dual-function immune evasion mutation, it will not only exhibit high replicative and transmission fitness but also evade both innate and adaptive immune responses. This is precisely where I anticipate that highly C-19–vaccinated populations will generate an evolutionary environment conducive to increased viral virulence (see the diagram below). Of course, as the immune forces currently at play are no longer selective, purifying selection is increasingly contributing to the slowdown in the dominant circulation of new immune escape variants. This delay in the evolutionary trajectory of newly emerging immune escape variants toward (co-)dominance leaves public health authorities with the illusory impression that the pandemic is finally transitioning into a stable equilibrium between population-level immunity and the virus—thanks, ostensibly, to the mass vaccination program!!

As explained extensively before, what we are currently witnessing is not a true equilibrium, but rather a metastable one— one that can easily be disrupted by a small additional perturbation (i.e., a few extra mutations, even ones that may be detrimental to viral fitness!), creating just enough added tension to cause sudden destabilization—making the elastic snap and thereby rendering a newly emerging immune escape variant highly virulent!

As I have long warned, “Society in Highly C-19–Vaccinated Countries Will Be Caught by Surprise,” as the rise of increasingly immune-subversive SC-2 variants diverts the attention of the medical community toward all kinds of other infectious and non-infectious diseases—many of which are increasing in prevalence due to vaccine breakthrough infection (VBTI)-associated immune dysregulation. Meanwhile, few anticipate the emergence of a novel, highly infectious, and fully immune-resistant variant that could exploit an enormous transmission advantage, culminating in rapid global dominance and the onset of a new, highly virulent pandemic. Indeed, no one is anticipating such a sudden and dramatic shift in highly C-19 vaccinated populations. The current spread of NB.1.8.1 and the associated rise in disease cases is not yet recognized as the harbinger of this disastrous but inevitable evolution.

If my analysis is correct, one should expect HIghly VIrulent OmiCRON descendants (HI-VI-CRON) to emerge in these highly C-19 vaccinated populations—particularly among individuals with weakened or untrained cell-based innate immunity (i.e., primarily elderly and adult individuals), and especially during the hot season! Summer will therefore reveal whether the title of my book was justified: 'The Inescapable Immune Escape Pandemic'."

In summary: Beyond the well-documented direct side effects of the mRNA-based 'vaccine' injections, highly vaccinated C-19 populations are now increasingly witnessing excess mortality due to vaccine-associated immune dysregulation. This is the result of immune escape, a phenomenon that, for example, arises from the improper deployment of the immune system’s ‘special forces’ (i.e., B and T cells), such as through mass vaccination during a pandemic, or through improper training of these special forces, such as by using mRNA-based 'vaccines'.
Both scenarios lead to immune refocusing, which either generates or sustains immune escape and thereby leads to repeated VBTIs. Due to immune refocusing, highly C-19 vaccinated populations exert immune pressure on the virus — initially selective, but ultimately non-selective — causing viral evolution and the intra-host amplification of new immune escape variants in chronically SC-2-infected hosts to proceed increasingly slowly. As a result, inter-host transmission becomes compromised, creating a natural positive selection among already highly infectious variants for specimens that, due to harboring mutations which actively suppress or evade innate immune sensing (e.g. via changes in NSP1, ORF6, or dsRNA processing), acquire increased transmission fitness — even if this comes at a fitness cost (and thus they may be relatively harmless to the unvaccinated population!).
However, mutations that impair immunoinflammatory signaling, or otherwise prevent activation of antigen-presenting cells (APCs), inevitably further weaken the already dysregulated adaptive immunity, which then completely loses its disease-protective function. Together with the compromised innate immunity, this opens the door wide to increased viral virulence.

In Conclusion: As a matter of fact, it seems that undermining the last bastion of the host’s innate immunity has now become a conditio sine qua non for the virus to enhance transmission and ensure survival in the population. However, downregulation or impairment of innate immunoinflammatory signaling or virus uptake by APCs—processes necessary to prime adaptive immune responses such as T and B cell activation—will further compromise an already maladaptive immune response. This response has been massively mobilized and served as the cornerstone of protection against symptomatic VBTIs, despite all the immune dysregulation and associated disorders it generated.
It seems, therefore, that viral survival will inevitably be associated with enhanced virulence, and there is little immune buffer capacity left to delay a spectacular wave of hyperacute systemic disease in highly C-19 vaccinated populations.

Although highly compelling, the above-described evolutionary mechanism is unprecedented in the history of clinical virology and underappreciated by our public health authorities. They prefer to learn by watching from the sidelines. This is perhaps the most unbelievable—but real—example of irresponsible behavior from an official authority that should have only one priority: protecting people’s health! Instead, they have orchestrated a large-scale gain-of-function experiment on the human species, leading to convergent evolution of dramatic immune dysregulation and catastrophic viral immune escape.

So, Africa, when your victory is a done deal, it will be up to you to take the lead.’

___

You must not wait for another catastrophic crisis (at times manufactured but we are prevented from making our own basic personal decisions or accessing needed drugs and response tools) to catch you off-guard. We must take charge and be prepared today so that we can enjoy peace of mind tomorrow.

Enter the Wellness Company as a solution and a willing participant in the health care conversation. The Wellness Company, launched in 2022, offers health care, prescriptions, and supplements, all backed by research

The Wellness Company isn’t chasing profits — it’s trying to help people recover. While the government continues pushing vaccines, The Wellness Company is focusing on real solutions.

From telemedicine, prescriptions, memberships, and supplements, TWC is leading America with alternative choices to the traditional health care model.

Please consider support of a good PATRIOT company (in this PATRIOT economy) Drs. McCullough, Risch, Thorp, myself support (they are our sponsors), The Wellness Company; see the emergency preparation kit (key component being antibiotics you were denied by doctors, pharmacists, governments during the fraud COVID), first aid kit, travel emergency kit, contagion control kit etc. Please consider the SPIKE SUPPORT (spike protein DETOX dissolving spike from mRNA vaccine, this is critical to remove spike form the mRNA vaccine/and DNA viral vector) formula with NATTOKINASE as well as the triple formula (SPIKE SUPPORT, BROMELAIN, CIRCUMIN)

If you wish to give a donation to help me, you can at:

Zelle:

sr7283@gmail.com

Or Ko-Fi

Ko-fi.com/drpauleliasalexander

Or to my address at:

150 South 8th Street

Unit 170

Lewiston, New York

14092

Alternatively, please consider going from an UNPAID subscriber or follower to a PAID at $5 per month or $30 per year. This can provide me help. If this is not possible at this time, this is ok, please remain a subscriber for FREE and there is no difference between FREE and PAID. No restrictions.