How COVID Shots
Suppress Your Immune System
Analysis by Dr. Joseph Mercola
February 06, 2022
STORY AT-A-GLANCE
In a non-peer-reviewed
research paper just this week published, Stephanie Seneff, Ph.D., describes a
mechanism of the COVID shots that results in the suppression of your innate
immune system. It does this by inhibiting the type-1 interferon pathway
The COVID jab can
cause neurons in your brain to produce toxic spike protein, or take up
circulating spike protein, and the neurons try to eliminate the spike protein
by transmitting them through exosomes. The exosomes are picked up by microglia,
immune cells in your brain, which activate an inflammatory response, which can
contribute to degenerative brain disorders
Two microRNAs,
miR-148a and miR-590, are central in this process. These microRNAs — excreted
in the exosomes along with the spike protein — significantly disrupt the type-1
interferon response in any cell, including immune cells
On average, there are
twice as many reports of cancer following the COVID shots compared to all other
vaccines combined over the last 31 years.
The fact that the
signal is that strong is even more remarkable when you consider that most
people don’t think the COVID shot could be a variable in their cancer
emergence, so they never report it
In this interview,
return guest Stephanie Seneff, Ph.D., a senior research scientist at MIT who
has been at MIT for over five decades, discusses her latest paper, "Innate
Immune Suppression by SARS-CoV-2 mRNA Vaccinations. The Role of G-quadruplexes,
Exosomes and MicroRNAs," co-written with Dr. Peter McCullough, along with
two other authors, Dr. Greg Nigh and Dr. Anthony Kyriakopoulos.
Previously, Nigh and
Seneff co-wrote an entire paper detailing the differences between the spike
protein and the COVID jab spike protein. In a non-peer-reviewed research paper
just this week published on the pre-print service authorea, they and their
other co-authors delve deeply into the mechanisms of the COVID shots, showing
how they absolutely, in no way, shape or form, are safe or effective. The shots
actually suppress your innate immune system.
"I think
McCullough is fantastic and I'm so happy to have him collaborate with me,"
Seneff says. "I really hope we will be able to find a journal that is
willing to publish it. We may have to seek some kind of alternative media to
get it published.
It's really incredible
the amount of censorship that's going on right now. I'm in a state of shock all
the time. I just keep thinking it's not going to get any worse, and it's truly
going to get better, and it just seems to keep on getting worse and worse.
I don't know where the
end is. It's very discouraging ... Pharma has so much money behind [them] and
they've got it all set up to make sure that nothing gets past them ...
We're hoping to put it
up as a preprint, but ... remarkably, they can reject it at the level of
preprint as well. We're working on that angle, but it's not easy. When you're
writing something this radical, they really fight hard to keep it off the
web."
On January 16, 2022,
the pre-print service Authorea published this paper on its web site, assigning
it a DOI, thus making it official.
Exceptionally Strong
Safety Signals
As noted by Seneff,
when you look at the various databases for adverse effects, you can see an
exceptionally strong safety signal — and the COVID shot developers know that.
"The numbers are out of sight," Seneff says, and this goes for all
levels of side effects, from mild to catastrophic.
Seneff has been
looking at the cancer data, for example, and on average, there are twice as
many reports of cancer following the COVID shots compared to all other vaccines
combined over the last 31 years.
"It's just
amazing, because it's overall two times [higher]. Breast cancer, for example,
is three times [higher] for these vaccines in one year, as they are for all the
other vaccines for 31 years. It's a hugely strong signal," Seneff says.
"Lymphoma is also
showing up much more frequently with these [COVID shots]. There's just an
amazing signal there in VAERS [the U.S. Vaccine Adverse Events Reporting
System]."
The fact that the signal
is that strong is even more remarkable when you consider that most people don't
think the COVID shot could be a variable in their cancer emergence, so they
never report it. "It puzzles me that they're willing to do such damage to
the health of the whole population of the world. I don't understand that degree
of evilness," Seneff says.
Type-1 Interferon
Disruption
The shots suppress
your innate immune system by inhibiting type-1 interferon. One of the first
studies to tip off Seneff and McCullough to this was an Indian study, in which
human cells grown in a culture were exposed to the DNA nanoparticles that
instruct them to make SARS-CoV-2 spike protein, much like the COVID shots do.
The cell strain is
called HEK-293. These are cells that were taken from the kidneys of an aborted
fetus in the 1980s and are frequently used in research. While taken from the
kidneys, these cells have neuron-like properties. When programmed to make spike
protein, these cells release that spike protein inside exosomes — lipid
nanoparticles inside which the spike protein is packaged.
Exosomes act as a
communication network for cells. When a cell is under stress, it releases
exosomes containing some of the molecules that are stressing it. So, in the
case of the COVID shots, the exosomes contain spike protein and microRNA.
MicroRNAs are signalling molecules that are able to influence cell function.
They cause the cell to change its behavior or metabolism. Typically, they do
this by suppressing certain enzymes.
The Indian study found
two specific microRNAs inside the exosomes released by these neuron-like cells:
miR-148a and miR-590. The researchers then exposed microglia (immune cells in
your brain) to these exosomes. So, as explained by Seneff, you've got neurons
in your brain producing spike protein, or taking up spike protein that is in
circulation, and reacting to it by releasing exosomes.
The exosomes are then
picked up by microglia, the immune cells in your brain. When the immune cells
receive those exosomes, they turn on an inflammatory response. This is
primarily a response to those microRNAs, the miR-148a and miR-590. Of course,
you also have the toxic spike protein there.
Combined, they cause
inflammation in the brain, which damages neurons. This inflammation, in turn,
can contribute to a number of degenerative brain disorders. The lipid particles
in the COVID shot, which contain the mRNA, are similar to exosomes, but not
identical. They're also very similar to low-density lipid (LDL) particles.
"I think the
exosomes are probably quite a bit smaller. The vaccine particles are bigger.
They're more like an LDL particle. The vaccine particles have cholesterol in
their membrane, and they have lipoprotein. So, they're made to look like an LDL
particle.
But then they throw in
this cationic lipid, which is really, really toxic — a synthetic cationic lipid
that makes it positively charged. Experimentally, they've found that this
lipid, when the particle is taken up by the cell, is released into the
cytoplasm, [where] that mRNA then makes spike protein.
[The COVID shots] are
very cleverly designed, both in terms of protecting the RNA from getting broken
down, and in terms of making the RNA be very efficient at making spike protein.
It's very different from the mRNA that the virus makes, even though it codes
for the same protein."
Seneff wrote an entire
paper detailing the differences between the viral spike protein and the COVID
jab spike protein, together with Greg Nigh, which was published in the
International Journal of Vaccine Theory, Practice and Research in May 2021. It
basically serves as a primer for understanding what we discuss here.
Two microRNAs,
miR-148a and miR-590 — excreted in the exosomes along with the spike protein —
significantly disrupt the type-1 interferon response in any cell, including
immune cells.
Getting back to the
Indian paper cited above, they found that the microglia ended up producing
inflammation in the brain, and the two microRNAs were central in this process.
The miR-148a and miR-590 were put into those exosomes with the spike protein,
and these two microRNAs are able to significantly disrupt the type-1 interferon
response in any cell, including immune cells.
Type-1 interferon also
keeps latent viruses like herpes and varicella (which causes shingles) viruses
in check, so if your interferon pathway is suppressed, these latent viruses can
also start to emerge. The VAERS database reveals many who have been jabbed do
report these kinds of infections. Suppressed interferon also raises your risk
of cancer and cardiovascular disease.
Type-1 Interferon
Response Is Crucial in Viral Infections
As explained by
Seneff, the type-1 interferon response is absolutely crucial as the first-stage
response to a viral infection. When a cell is invaded by a virus, it releases
type-1 interferon alpha and type-1 interferon beta. They act as signaling
molecules that tell the cell that it's been infected.
That, in turn,
launches the immune response and gets it going early in the viral infection.
It's been shown that people who end up with severe SARS-CoV-2 infection have a
compromised type-1 interferon response. As noted by Seneff:
"It's ironic that
the vaccines are being given to protect you from COVID, yet, they produce a
situation where your immune cells are ill-equipped to fight SARS-CoV-2 if it
gets into the cell. The trick is, the vaccine produces a tremendous antibody
response, and that's typical of severe disease.
So, the [COVID shot]
fools your immune system into thinking that you've had a severe case of COVID.
It's really interesting that way, because it's gotten past the mucosal barrier
of the lungs, it's gotten past the vascular barrier of the blood, into the
muscle. Also, it's been disguised.
The RNA doesn't look
like a virus RNA, it looks like a human RNA molecule. Part of the modifications
[made to the mRNA in the jab] was to make it very sturdy, so it can't be broken
down. It's also very good at making [spike] protein fast, which also has a
problem because it leads to a lot of errors, which is another issue ...
The immune cells take
up the nanoparticles and carry them through the lymph system into the spleen.
Multiple studies have shown that it ends up in the spleen ... the ovaries, the
liver, the bone marrow ... The spleen, of course, is very important for
producing antibodies."
Importantly, the
antibody response you get from the COVID shot is exponentially higher than what
you get from natural infection, and research has shown that the level of
antibody response rises with disease severity. So, the shot basically mimics
severe infection. In mild infection, you may not produce any antibodies at all,
because the innate immune cells are strong enough to fight off the infection
without them.
It's when your innate
immune system is weak that you get into trouble, and part of that weakness is a
suppressed type-1 interferon response. If your type-1 interferon response is
deficient, your immune cells are not very capable of stopping the spread of the
virus in your body.
According to Seneff,
the reason type-1 interferon supplementation has not been recommended thus far
is because you have to time it perfectly in order for the immune cascade to
function properly. Type-1 interferon plays a definitive role only at the very
earliest stage of the infection. Once you've entered a moderate or severe
infection stage, it's too late to use it.
COVID Shots Confuse
Your Immune System
As noted by Seneff,
the COVID shots are so unnatural that your immune system doesn't quite know
what to do anymore.
"My impression is
that the immune cells don't know what the hell's going on. There's this toxic
protein being produced in massive amounts by the immune cells. That's extremely
unusual. There's no sign of any kind of viral infection because these RNAs look
like human RNAs.
It's as if the human
immune cells suddenly decided to make a really toxic protein, and make lots of
it — which is exactly what they're doing — and the immune system is completely
baffled by this. The immune cells have no clue what to do with it.
Of course, these
immune cells that are overloaded with all this spike protein, they say, 'I've
got to get rid of this stuff,' so they ship it out as these exosomes. The
microRNAs [in the exosomes] think that the recipient cells are going to need
those particular signalling molecules to help it do whatever it needs to do to
cope with this toxic load.
So, you're spreading
the spike protein around to the rest of the body, just to dissipate the
toxicity you're coping with in the spleen, I think. Those exosomes are also
very good for training antibodies. There was a nice paper that showed the
exosomes being released [have] spike protein in their membrane, the exterior of
the exosome.
It's quite cool that
the spike protein is displayed there, because this allows the immune cells —
the B-cells and the T-cells that need to get up close and personal to it — to
figure out how to shape their antibodies. The antibodies get shaped to match
the toxic protein that's exposed on the surface of the exosomes.
After something like
14 days of the second [jab], the exosomes induced an antibody response. [The
researchers] felt the exosomes played a critical role in this extreme antibody
response that was produced by the B-cells and the T-cells, the adaptive immune
system.
But I think the way
the vaccine works is that there's no game that you can choose other than to
make antibodies. It's the only way you can fight this. It's a toxic protein
that's being produced and released by these immune cells, and the only thing
you can do to stop it is to make antibodies.
They try to make lots
and lots of antibodies that will glue onto those toxic spike proteins and block
them from being able to get in through the ACE2 receptor. That's the job of the
antibodies. They do a good job of it, initially ... It's true that they do
protect you from disease. Unfortunately, the antibody levels drop pretty
dramatically, pretty quickly."
There are also
antibodies that enhance disease rather than fight it, and the level of these
antibodies declines at a slower pace than the protective antibodies. So, after
a number of months you end up with a NEGATIVE immune response. In other words,
you're now more prone to infection than ever before. As explained by Seneff:
"There's a
crossover point at which the enhancing antibodies can be stronger than the
protective antibodies, and that's when you can get this antibody dependent
enhancement (ADE) that people have seen in the past with [other] coronavirus
vaccines. We're still trying to see if that's the case with [the COVID jabs].
There is some evidence here and there, but it's not [conclusive yet]."
The Importance of
Cytotoxic T-Cells
After the India study
tipped off Seneff and McCullough to the interferon problem, they came across a
Chinese study that tracked the effect of the COVID jab on the immune system
over time. Here, they discovered that the infection caused an increase in CD8+
T-cells, important cytotoxic T-cells that actually remove infected cells.
As noted by Seneff,
the CD8+ cells are an important part of the defense against SARS-CoV-2.
Importantly, CD8+ T-cells were enhanced in response to natural infection, but
not in response to the COVID shot. They too found type-1 interferon suppression
post-jab. So, in the aftermath of the jab, not only is your first-line response
depressed — the type-1 interferon response — but you're also missing the part
of the immune response that cleans away infected cells.
The microRNA That
Influences Myocarditis Risk
A third microRNA
(mRNA) created by natural SARS-CoV-2 infection is miR-155, and it plays an
important role in heart health. Early on in the pandemic, there were reports of
COVID-19 causing heart problems.
Seneff suspects the
miR-155-containing exosomes may also be present post-jab, and may play a role
in the heart damage that's being reported. Specifically, miR-155 is associated
with myocarditis. As mentioned earlier, microRNA suppresses certain proteins
that then cause a complicated cascade response. When a particular protein that
is a critical player gets suppressed by a microRNA, then a whole different
cascade takes place.
Why Autoimmune
Problems May Arise Post-Jab
The antibodies
produced by the jab also have several short peptide sequences in them that have
previously been found in several human cells that are related to autoimmune
disease. Seneff explains:
"Kanduc has
written a lot about this. She's an expert on these antibodies ... The
[SARS-CoV-2] spike protein is very overlapped with human protein. That means
when you build a really strong antibody response to the spike protein, those
antibodies can get confused and they can attack a human protein that has a
similar sequence.
That's a classic form
of autoimmune disease. It's called molecular mimicry. There were many different
proteins that matched. It was quite surprising ... It seems to be very well
designed to induce autoimmune disease, if you produce antibodies to those sequences
in the spike protein."
Neurological Problems
in Women
The shots are also
tightly associated with neurological problems such as uncontrollable tremors
and shaking. Curiously, this side effect disproportionally affects women. The
mechanism here again involves the exosomes. Seneff explains:
"I feel there's a
very strong signal for the idea, which I'm pushing, that you have those immune
cells in the spleen making spike protein and releasing it in exosomes. It's
been shown in studies on Parkinson's disease that those exosomes travel along
nerve fibers.
They'll go along the
splanchnic nerve, they'll hook up with the vagus nerve, they'll go up to the
brain and get into all these different nerves in the brain. When you look at
the VAERS database, you see tremendous signals for all kinds of things that
suggest different nerves are being inflamed.
For example, there are
12,000 cases of tinnitus associated with the COVID-19 vaccine, and that's only
what's reported. Tinnitus is a strong signal. Tinnitus is going to be
inflammation of the auditory nerve. This means you have to go all the way from
the spleen, up the vagus nerve, and then connect to the auditory nerve to cause
tinnitus.
Then you have Bell's
palsy, which is inflammation of the facial nerve. You have migraine headache.
There are over 8,000 cases of migraine headache, which is linked to an
inflammation of the trigeminal nerve.
It probably also goes,
I suspect, along the nerve fibers of the spinal column, which may be causing
some of these cases where they're finding paralysis. People have a lot of
mobility issues connected with these vaccines.
I see the possibility
of causing a lot of disturbances to the myelin sheath, and we talk about that
in the paper. It involves, again, complex signaling. You can get to the myelin
sheath problem through the type-1 interferon disruption.
That, again, involves
something called interferon response factor 9 IRF9. This protein triggers the
production of sulfatide in the liver, and this protein gets suppressed by these
microRNAs that I mentioned earlier."
Sulfatide, an
important lipid carrier, is the only sulfonated lipid in the human body. Your
liver makes most of the sulfatide, which is then carried by your platelets
(blood cells) to other areas in your body. The myelin sheath contains high
amounts of sulfatide. It's part of what protects the myelin sheath. In
demyelinating diseases, that sulfatide erodes, ultimately allowing the myelin
to be attacked.
Seneff believes the
COVID jab results in significant myelin damage, thanks to these inflammatory
exosomes. This damage does not necessarily show up right away, although some
jab recipients experience acutely devastating effects.
It could take
10 years or more before a demyelinating disease sets in.
"I think we're
going to see people getting these neurodegenerative diseases earlier and
earlier in life than they used to," Seneff says, "and I think anybody
who already has any of these diseases is going to have accelerated
progression."
We May Soon See an
Explosion of Parkinson's Cases
Disturbingly, loss of
smell and dysphagia, the inability to swallow, are both signs of Parkinson's
disease, and both of these conditions are being reported post-jab by the
thousands. So, in years to come, we could be looking at an explosion of
Parkinson's.
"Parkinson's
studies have shown that you can get pathogens in the gut that produce a
prion-like protein, which is what the spike protein is. The immune cells then
take it up and take it to the spleen. This, of course, causes stress.
A stressed immune cell
in the spleen upregulates and produces more alpha-synuclein. Alpha-synuclein is
a molecule that fights infection, and that's the molecule that misfolds in
association with Parkinson's disease.
I'm fascinated with
all of these molecules that are prion-like. There's the prion protein itself,
which is associated with CJD, Creutzfeldt-Jakob disease, but then there's the
alpha-synuclein and amyloid beta, there's TDP-43, which is associated with ALS.
All of those diseases
are overrepresented in the VAERS database for the COVID shots, compared to all
the other vaccines combined over 31 years. It's just completely out of line.
There are 58 cases of
Alzheimer's in association with the COVID vaccines, and 13 in association with
all the other vaccines over 31 years. That's several times more — 58 versus 13.
CJD is also much more
common. It's almost seven times as common in the COVID vaccine cases. CJD is a
terrible disease. You get very crippled and die after a few years. That's the
classic prion protein [disease]. It's extremely rare. Only 1 in 1 million gets
CJD.
There was a person who
contacted me from France whose wife got CJD just a few weeks after the second
vaccine. He was absolutely convinced the vaccine caused it. There are actually
27 cases [of CJD] reported in VAERS for the COVID-19 vaccines, against only
four cases over the entire history of all other vaccines combined."
Health Problems We Can
Expect to See More Of
In time, Seneff
predicts we'll see a dramatic increase in infections and cancers of all types,
autoimmune diseases, neurodegenerative diseases and reproductive issues. As
mentioned, research has demonstrated that the spike protein accumulates in the
spleen and women's ovaries.
Without doubt,
inflammation in the ovaries is not a good thing. Men also report swollen
testes, and that could be indicative of inflammation as well. Preliminary data
show women who get the jab within the first 20 weeks of pregnancy have a miscarriage
rate of 82% to 91%. There are also VAERS reports describing fetal damage. Of
course, it could also impair future fertility.
As described earlier,
some antibodies produced by the jab can react to human proteins. One protein
that is similar to the spike protein that the antibodies attack is syncytin,
which is essential for the fertilization of the egg. The concern is that the
antibodies might attack and destroy syncytin, thereby disrupting and preventing
implantation in the placenta.
Omicron — A Blessing
in Disguise ?
The jabs also
perpetuate COVID, with ever-new variants of the virus.
"In the first
paper that Greg and I wrote, we predicted the vaccines would cause an increased
emergence of variants of spike protein, altered versions of the virus, under
the pressure of the vaccine," Seneff says.
"Indeed, it looks
to me like that's what's happening. But I'm really hopeful with Omicron,
because Omicron looks like it's a milder virus, but incredibly infectious.
It'll flash through the population and give everybody, essentially, a vaccine.
It's kind of like a natural vaccine, I think.
[Research] showed that
... having had Omicron, you were protected, to some extent, from Delta. Delta's
disappearing anyway, because Omicron is chasing it out. It's really great. I
think Omicron is God's gift from heaven."
That blessing may be
canceled out in those who have received multiple COVID jabs, however. Each dose
erodes your immune response, such that it becomes increasingly compromised with
each jab. Again, this has to do with the suppression of type-1 interferon,
discussed earlier.
What Catalyzes Damage
in Athletes ?
More than 400 cases of
serious heart problems and death have also been reported among professional
athletes, who are some of the healthiest people on the planet. What mechanism
can account for this phenomenon ? How is it that the COVID jabs can cause
enough damage to take out young people with optimized biology ?
Seneff suspects that
being fit might cause you to have more ACE2 receptors in the heart, and the S1
portion of the SARS-CoV-2 spike protein binds to the ACE2 receptor. She
believes the spike protein is being delivered to the heart via exosomes, by way
of the vagus nerve, and, again, the miR-155 exosome is associated with heart
problems.
Additionally, when the
S1 spike protein binds to the ACE2 receptor, it disables the receptor. When you
disable ACE2, you get an increase in ACE, which causes high blood pressure and
elevates angiotensin 2. When angiotensin 2 is overexpressed, you can get
intense inflammation in the heart. If you're engaging in intense exertion and
your heart is inflamed, you can trigger cardiac arrest, which is what we see in
many of these athlete cases. They're collapsing on the field.
G-Quadruplexes
Another focus of
Seneff's and McCullough's paper is something called G4 or G-quadruplexes.
"G-quadruplexes
are really fascinating, and I don't have a handle on them at all," Seneff
says. "It's hard biology, even harder than a lot of the other stuff that
I've been reading ...
G4s are basically an
arrangement of [guanines]. Guanines are one of the four nucleotides that make
up DNA or RNA. Guanine is the G in the G4. What happens is that a sequence of
nucleotides on a DNA or an RNA string can fold in on itself and form G-quadruplexes.
It's four guanines, at different places on the protein, winding back around and
sticking together.
There's a metal in the
middle — often potassium or calcium — that helps to stabilize these G4s. The
interesting thing about them is that they make the water around them
structured. They make gelled water [aka exclusion zone (EZ) water] ...
Those G4s can form in
the DNA, and that actually keeps it from becoming active. [The DNA] doesn't get
converted into RNA, and it doesn't make protein if it has those G4s. Probably,
the EZ water doesn't allow anything to get close. Think of it as being stuck in
a gel.
There are a lot of G4s
in the promoter regions of these DNA sequences, and there are lots of proteins
that have these G4s in their promoter region. Interestingly, there are certain
proteins that can unravel them. There are proteins that can bind to them and
cause the G4 to undo, and that activates or allows the protein to be expressed.
It's a regulatory
element that controls which proteins get to be expressed from the DNA. Many of
the proteins that have these G4s in their promoter are cancer oncogenes. As
long as they stay gelled, they're inactive, but if they become ungelled, they
become active.
It turns out that
prion proteins ... [are] made from RNA, and the RNA has these G4s. The protein
can bind to the G4s in the RNA and both of them react. The theory is that the
protein becomes prion-like. These prion proteins have two ways to be, one is
safe and one is not safe, and the G4s increase the risk for prion protein
misfolding.
The presence of those
G4s, and the meeting with those G4s, increases the risk of misfolding in the
prion-like configuration. The interesting thing about that is that spike
protein is a prion-like protein. The RNA they built for the [COVID jab], they
did something called codon optimization, which involved putting a lot more
guanines into the RNA than [found] in the original [virus]. They enhanced the
guanine.
Enhancing the guanine
means increasing the number of G4s, which means increasing the risk of the
spike protein misfolding into a prion like protein. I think that the G4s
increase the risk, the danger of spike protein [acting] as a prion-like
protein.
But we don't really
know what the consequence of having all these G4 RNAs in the cytoplasm will be.
We have massive numbers of these RNAs sitting there with their G4s. What is
that going to do to the rest of the G4 regulatory process? We do not know.
Nobody knows. Nobody has a clue."
Summary
To summarize the
central point of Seneff's latest paper, the COVID jab causes alpha interferon
suppression, which weakens your immune system. Indeed, regulators in the
European Union are now warning that repeat COVID shots can weaken overall
immunity.
The primary mechanism
is the impairment of alpha interferon response, which is essential for the
proper activation of your innate immune system, your cellular immunity, mostly
your T-cells and killer cells. When functioning properly, the cell launches the
type-1 interferon response as soon as it's infected with a virus.
It triggers the immune
cells to come in, kill the virus and remove the debris. This activates the
humoral component of your immune system, the antibody production, which takes
longer. (That's why they say you are not protected until 14 days after the
injection.)
How is type-1
interferon suppressed by the jab ? It's suppressed because type-1 interferon
responds to viral RNA, and viral RNA is not present in the COVID shot. The RNA
is modified to look like human RNA molecule, so the interferon pathway is not
triggered. Worse, the interferon pathway is actively suppressed by the large
number of spike proteins produced from the mRNA in the shot, and by the
microRNAs in the exosomes released by the stressed immune cells.
related:
Rare Multisystem
Inflammatory Syndrome Detected in Vaccinated Young
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