Is there any amount of information that can emerge regarding the dangerous vaccines that will prompt Republicans to take the issue seriously? Lives, liberties, careers, and human experiences were destroyed because of these shots, millions are dead and injured, and countless more need long-term treatment and cures. Yet, rather than mass vaccination being questioned, the full force of government funding, promotion, and indemnification is backing the next iteration of these shots. Anyone home? It only affects all of humanity.

What any layman should have learned from the past few years is that pumping an uncontrolled spike of antibodies into one’s body is not necessarily safe or even effective. God designed our bodies to produce the right sort of antibodies in the right amount at the right place in the right time. What happens when you pump someone’s body with an endless litany of antibodies over a relatively short period of time, particularly with regard to respiratory viruses? Well, you get uncontrolled antibodies, which include problematic classes. A pair of new, peer-reviewed studies now shed light on why the vaccines induced negative efficacy and are associated with so many autoimmune syndromes. These studies also paint a concerning picture for the endless litany of vaccines the authorities will have coming down the pipeline ... if we fail to stop them.

Remember that Cleveland Clinic study of over 50,000 health care workers that found that "the higher the number of vaccines previously received, the higher the risk of contracting COVID-19"? Well, now it’s peer-reviewed, and the correlation showing the more you inject, the more you infect is unmistakable.

The Cleveland Clinic researchers posit as a possible culprit for negative efficacy the fact that “[classes] switch towards non-inflammatory spike-specific IgG4 antibodies after repeated SARS-CoV-2 mRNA vaccination.” Several studies have found shockingly high levels of “tolerating” IgG4 antibodies in those jabbed with the COVID shot, which is one of the most alarming discoveries to date. It might illuminate the reason for both the negative efficacy and the plethora of side effects from the shots often being much longer term than the damage even from the spike protein.

To that end, a compelling German study, which was just recently peer reviewed, found “a remarkable increase in IgG4 levels” among “people who were administered two or more injections of the mRNA vaccines.”

We already know that IgG4-tolerating antibodies are inappropriate for dealing with pathogens. For those who received multiple doses of mRNA, it actually trains their bodies to tolerate rather than fight the virus it was designed to destroy. The other class of blood-based antibodies (IgG1 or IgG3) is designed to neutralize pathogens; however, the IgG4 class was specifically designed to tolerate innocuous cells (that don’t reproduce) that it repeatedly contacts, such as pollen or peanut particles. They serve an important role and help ensure that people don’t respond with excessive inflammation to everyday encounters with pollen, but to see 20% of the antibody response to SARS-CoV-2 (it was as high as 42% in those experiencing infection after boosters) be something that tolerates it is astounding.

The revelation about the antibody class-switch to IgG4 might be the reason why a recent CDC conference resulted in a massive COVID outbreak — even though COVID barely exists in most communities today. If there is any pool of people who likely got an embarrassingly high number of boosters, it would be CDC employees.

But in addition to serving as a Trojan horse for the virus, which might explain the negative efficacy, high levels of IgG4 itself are dangerous. According to the German study published in Vaccines, "Increased IgG4 synthesis due to repeated mRNA vaccination with high antigen concentrations may also cause autoimmune diseases, and promote cancer growth and autoimmune myocarditis in susceptible individuals.” (emphasis added)

These are long-term concerns. Inappropriate classes of antibodies can attack the body with a myriad of autoimmune syndromes. Also, aside from spike-induced myocarditis, the study found that the misfiring of antibodies can also attack the heart muscle. The cancer finding is particularly concerning. Your immune system is just as prominent in fighting cancer as it is viruses. Thus, any misallocation of resources to the wrong class of antibodies will necessarily tamp down the killer cells needed to attack cancers.

“More IgG4 seems to be linked to more aggressive cancer growth, and both were strongly associated with higher cancer malignancy and poor prognosis,” warned the authors. “It was discovered that IgG4 can contend with IgG1 in binding to Fc receptors present in some immune cells in vitro. This competition results in the inhibition of typical immune responses against cancer cells, such as cell and complement cytotoxicity and cell phagocytosis, which are mediated by IgG1 antibodies.”

How can our government continue promoting these shots? Although most people wouldn’t be caught dead getting another shot, pregnant women are bullied into staying “up to date” on their schedule. Additionally, our government continues to fund these shots with other similar experimental vaccines to the tune of billions, so much so that House Republicans preserved such COVID funding in the debt ceiling deal.

Over the next few weeks, the appropriations subcommittees will be finalizing the annual appropriations bills. Conservatives must demand that Robert Aderholt, chair of the subcommittee overseeing HHS, and Andy Harris, chair of the subcommittee overseeing the FDA, jettison all funding for COVID shots. It is shocking how Republicans to this day have refused to broach the vaccine issue. How many more people have to die before we stop funding this poison, much less ban the technology from the market?