Booster-Caused IgG4 Immune Tolerance Explains Excess Vaxx Mortality

Source: (https://bit.ly/3I4BtX6)
Rintrah Radagast posted a very important article yesterday.
It shows us a potential explanation of why excess mortality
is related to COVID boosters, why the association of Covid
vaccines with mortality strengthens as time goes on instead
of declining, and why boosted people take the longest to clear
Covid-19.
Check Rintrah's article (https://bit.ly/3I4OeAZ) out. It is
brilliant and very disturbing.
Rintrah is discussing a very important scientific study that
answers a question: what exactly are those antibodies that
Covid-boosted people are developing?
This study answering that question is here
(https://bit.ly/3PWVhhc).
After mRNA vaccination the immune response against Spike
is shifting to IgG4, which is how your body responds after repeat
exposure to stuff it needs to tolerate, like bee venom, pollen or
peanut proteins.
Our immune systems are complicated. We do need to fight
dangerous replicating pathogens, such as viruses or bacteria. At the
same time, we also face harmless inert substances, such as tree
pollen, that sometimes cause inflammatory reactions called
allergies.
To deal with these harmless substances, our immune system has
a particular class of antibodies, called IgG4, that do the opposite
of what we are used to hearing: they bind to allergens and tell
our immune cells to ignore them rather than cause inflammation.
I had many pollen allergies. Every spring was unpleasant. I decided
to go to an allergist and take allergy shots, which amounted to
repeatedly injecting allergens into me. As a result of these repeat
antigen shots, my immune system developed non-inflammatory
IgG4 antibodies, which mark pollen as a harmless substance
to the rest of my immune system and prevent allergic inflammation
and nasty symptoms.
There is something important, though: pollen does not replicate.
It is a good idea not to have inflammation in response to pollen.
It is a bad idea, however, to train our immune system to ignore
replicating pathogens such as Sars-Cov-2.
How would "immune tolerance," induced by repeat antigen shots
such as mRNA injections, look like when the person is infected
with Sars-Cov-2?
It would look like a "mild" infection without a serious fever that
would last much longer than necessary and cause organ damage.
The sufferer may say, for the first week, that they are thankful for
vaccines and boosters making their symptoms mild. Then they start
wondering why the infection is not going away. 
https://bit.ly/3FVqsET
IgG4 antibodies have the opposite effect to all other types
of antibodies and make our immune system ignore the particular
antigen they are trained to detect.
You do not want to ignore a replicating virus - so the IgG4 antibody
class would be inappropriate for viruses. Pollen, however,
is a perfect case for IgG4 to prevent immune reaction and
inflammation.
Switching to IgG4 binding against a viral agent is like opening your
house doors wide for robbers and ignoring them as they ruffle through
your drawers. The robbery will be "mild" - but the thieves will take
away your stuff. And they will come back again.
Could repeat Covid infections, caused by immune tolerance, lead
to increased mortality? Absolutely! This Singapore study
(https://bit.ly/3WNoQns) suggests that most excess deaths
in Singapore happen within 90 days of a Covid infection. A lot
of such deaths, unfortunately, are not recorded as Covid deaths.
They could be recorded as "sudden deaths" from "unknown cause."
The disease may seem mild if immune tolerance fails to elicit
a strong reaction and stop viral replication. The virus,
proliferating unopposed, damages the cardiovascular system more
than in those who can mount a vigorous immune reaction. One such
victim is Gwen Casten, a 17-year-old daughter of vaccine-loving
congressman Sean Casten. Gwen died suddenly in her sleep in June
of 2022 after suffering a "very mild" Covid infection. 
It takes time for immune tolerance to develop after boosting. As the
Immunology article says (https://bit.ly/3vgpK0e):
These three individuals experienced the infection with the largest
time difference to the last vaccination, at 95, 201 or 257 days after
the second vaccination, while in the other nine patients the infection
took place between 25 and 78 days after the second mRNA shot. This
supports the hypothesis that the switch to IgG4 is a consequence
of ongoing GC maturation and that it takes several months until
IgG4-switched memory B cells appear.
This "taking months to develop" is a biological time bomb placed into
the immune systems of boosted people! It takes the germinal centers
months after the third injection to switch to the useless IgG4.
Therefore, many months after the booster dose, a Covid infection is
met with worthless, forgiving, and disease-ignoring IgG4 antibodies.
The infection seems mild; the virus replicates unopposed due to the
IgG4 switch; the cardiovascular system is damaged; the risk of sudden
death multiplies!