Studies demonstrate that survivors of the 1918 influenza pandemic (2 years old) possess highly functional, virus-neutralizing antibodies to this uniquely virulent virus, and that humans can sustain
Studies demonstrate that survivors of the 1918 influenza pandemic (2 years old) possess highly functional, virus-neutralizing antibodies to this uniquely virulent virus, and that humans can sustain
circulating B memory cells to viruses for many decades after exposure—well into the tenth decade of life; yes! Natural immunity is life-long, we know at least 100 years long! They LIED to you on vax!
Immunological memory is the ability of the immune system to quickly and specifically recognize an antigen that the body has previously encountered and initiate a corresponding immune response. Generally these are secondary, tertiary and other subsequent immune responses to the same antigen. Immunological memory is responsible for the adaptive component of the immune system, special T and B cells — the so-called memory T and B cells.
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IgG antibodies are Y-shaped protein molecules that are produced by special white blood cells (B lymphocytes) in response to foreign substances (antigens) such as viruses or bacteria. Antibodies can attach to these viruses or bacteria, rendering them harmless and unable to penetrate healthy cells. They GO AWAY with time and could fall to a NEGATIVE level DOESN'T mean susceptible.
.
Total immunity against viral diseases includes:
1. Local IgA and IgM
2. Humoral immunity of IgG antibodies, both those present in the blood AND those that can be produced quickly when the antigen is present
3. Cellular immunity or MEMORY
4. Other mechanisms.
When we measure antibody titers, we are ONLY documenting the IgG antibodies present in the bloodstream.
.
The Immune System fires up when a pathogen, like a virus, enters the body. The pathogen releases a protein called an antigen, which calls into action the immune system’s special disease-fighting cells. "Called B and T lymphocytes", these cells NOT only destroy the virus, but they REMEMBER what it looked like so they can fend it off in the FUTURE.
.
IMMUNOLOGIC MEMORY allows the immune system to REMEMBER the antigens or organisms to which it has previously been exposed. MEMORY EFFECTOR B cells (long-lived plasma cells) and MEMORY T-cells specific to a virus, give long-term immunity against these diseases.
.
ADAPTIVE IMMUNITY.
.
The “Adaptive Immune Response" is younger than the “Innate Immune Response" in evolutionary terms and is more specific and considerably MORE POTENT in its effects.
.
The constituents of the adaptive immune response are the lymphoid cells. These include:
.
The T lymphocytes and the cytokine and chemokine messenger proteins released by these cells, which direct and REGULATE the adaptive immune response.
.
The B lymphocytes, which transform to the late-stage plasma cells that produce and secrete antibody.
.
The lymphoid cells of the adaptive immune response reside in, and circulate between, the various lymphoid tissues of the body (e.g. the lymph nodes, spleen and mucosal lymphoid tissues). In the adaptive immune response, antigen is first transported from a site of infection by a dendritic cell to the regional lymphoid tissue. That dendritic cell in turn activates "Antigen-Specific T lymphocytes," which further activate Antigen-Specific B lymphocytes.”
.
These activated, Antigen-Specific lymphocytes must then be mobilized from the regional lymphoid tissue and sent to the site of infection, a process that involves these cells moving into the lymphatic and blood circulation and interacting with the endothelial lining of blood vessels.
.
Once these cells reach the site of infection, they are able to mount a full-scale ‘EFFECTOR’ response, which is considerably STRONGER than that permitted by innate immunity. As these processes take some time to occur (in the order of 4–7 days), there is a delay before adaptive immunity ‘takes over’ from the innate form of defence.
.
The final component of Adaptive Immunity is the development of a “REGULATORY RESPONSE" that will "SWITCH OFF" the system when it is NO LONGER REQUIRED (i.e. when the pathogen has been ELIMINATED) so as NOT to cause DAMAGE to normal body tissue.
.
HOWEVER, once this is achieved, the immune system retains the “MEMORY” of that immune response.
IMMUNOLOGICAL MEMORY is another key feature of the Adaptive Immune Response. MEMORY allows the generation of a much MORE effective SECONDARY IMMUNE RESPONSE (Anamnestic MEMORY Response) if that same antigen is EVER RE-ENCOUNTERED.
All those involved with the vaccines lied their tails off, because they knew billions in revenue was on the way. They also knew the vax were neither safe or effective, but the money was too great an incentive.
Natural immunity is lifelong as that is the nature of evolution. The critical part is what chemical was introduced in the months prior in that environmental setting that resulted in the influenza strain to mutate and spread, reaching outbreak point. With influenzas timing there were various changes to artificial fertilisers and that food was then provided to military personal which is where the outbreaks first manifest. Bacteria and Viruses are not enemies their friends trying to explain that the environment, and thus human consumption potential, has been altered and the mutation that presents as human illness is making adjustments to our system so the responsible chemical doesn't kill us. When the mutation is too vast a difference, acute and instant exposure, then it is "speaking in a language our cells can't understand and so it is deadly. When it is a slighter alteration, like from sub-acute exposure then it presents as a sickness. This is why we have over 3000 strains of beneficial e.coli in our gut and don't get sick from it yet a mutagenic e.coli say that's been exposed to Cadmium will result in e.coli poisoning. The e.coli is protecting the human system through illness so that we quickly excrete and the chemical doesn't cause even greater harms once absorbed.
They injected soldiers with a virus there was no Spanish Flu no virus has ever been isolated !!! No such thing as Covid !! They Tortured and Murdered my Father with a Fake PCR TEST AND DRUGGED HIM WITH REMDESIVIR AND A VENTILATOR UNTIL HIS ORGANS FAILED THEN TRIED TO KILL HIM WITH MORPHINE BUT HE WOKE UP SO THEN THEY USED FENTANYL NOT SOME FAKE VIRUS !!!!!
Question....whatever immunity was provided by the shots did not last long because the virus mutated into different strains. What is the difference with natural immunity that makes it life long? Or is natural immunity only effective against the strain it was created against?
How many people already had these circulating B memory cells for Covid by March 15th, 2020 (lockdown date)?
My answer: A lot.
The BIG FAT QUESTION is... why did the physicians vaccinated AFTER having COVID? They should have known better!!!!
AI exposes zero Government oversight on Pharma
https://scientificprogress.substack.com/p/system-failure-ai-exposes-zero-government
https://scientificprogress.substack.com/p/vaxxed-v-unvaxxed/
https://scientificprogress.substack.com/p/depopulation-or-extermination
https://scientificprogress.substack.com/p/depop-vaccines-no-myth
🔥
Immunological memory is the ability of the immune system to quickly and specifically recognize an antigen that the body has previously encountered and initiate a corresponding immune response. Generally these are secondary, tertiary and other subsequent immune responses to the same antigen. Immunological memory is responsible for the adaptive component of the immune system, special T and B cells — the so-called memory T and B cells.
.
IgG antibodies are Y-shaped protein molecules that are produced by special white blood cells (B lymphocytes) in response to foreign substances (antigens) such as viruses or bacteria. Antibodies can attach to these viruses or bacteria, rendering them harmless and unable to penetrate healthy cells. They GO AWAY with time and could fall to a NEGATIVE level DOESN'T mean susceptible.
.
Total immunity against viral diseases includes:
1. Local IgA and IgM
2. Humoral immunity of IgG antibodies, both those present in the blood AND those that can be produced quickly when the antigen is present
3. Cellular immunity or MEMORY
4. Other mechanisms.
When we measure antibody titers, we are ONLY documenting the IgG antibodies present in the bloodstream.
.
The Immune System fires up when a pathogen, like a virus, enters the body. The pathogen releases a protein called an antigen, which calls into action the immune system’s special disease-fighting cells. "Called B and T lymphocytes", these cells NOT only destroy the virus, but they REMEMBER what it looked like so they can fend it off in the FUTURE.
.
IMMUNOLOGIC MEMORY allows the immune system to REMEMBER the antigens or organisms to which it has previously been exposed. MEMORY EFFECTOR B cells (long-lived plasma cells) and MEMORY T-cells specific to a virus, give long-term immunity against these diseases.
.
ADAPTIVE IMMUNITY.
.
The “Adaptive Immune Response" is younger than the “Innate Immune Response" in evolutionary terms and is more specific and considerably MORE POTENT in its effects.
.
The constituents of the adaptive immune response are the lymphoid cells. These include:
.
The T lymphocytes and the cytokine and chemokine messenger proteins released by these cells, which direct and REGULATE the adaptive immune response.
.
The B lymphocytes, which transform to the late-stage plasma cells that produce and secrete antibody.
.
The lymphoid cells of the adaptive immune response reside in, and circulate between, the various lymphoid tissues of the body (e.g. the lymph nodes, spleen and mucosal lymphoid tissues). In the adaptive immune response, antigen is first transported from a site of infection by a dendritic cell to the regional lymphoid tissue. That dendritic cell in turn activates "Antigen-Specific T lymphocytes," which further activate Antigen-Specific B lymphocytes.”
.
These activated, Antigen-Specific lymphocytes must then be mobilized from the regional lymphoid tissue and sent to the site of infection, a process that involves these cells moving into the lymphatic and blood circulation and interacting with the endothelial lining of blood vessels.
.
Once these cells reach the site of infection, they are able to mount a full-scale ‘EFFECTOR’ response, which is considerably STRONGER than that permitted by innate immunity. As these processes take some time to occur (in the order of 4–7 days), there is a delay before adaptive immunity ‘takes over’ from the innate form of defence.
.
The final component of Adaptive Immunity is the development of a “REGULATORY RESPONSE" that will "SWITCH OFF" the system when it is NO LONGER REQUIRED (i.e. when the pathogen has been ELIMINATED) so as NOT to cause DAMAGE to normal body tissue.
.
HOWEVER, once this is achieved, the immune system retains the “MEMORY” of that immune response.
IMMUNOLOGICAL MEMORY is another key feature of the Adaptive Immune Response. MEMORY allows the generation of a much MORE effective SECONDARY IMMUNE RESPONSE (Anamnestic MEMORY Response) if that same antigen is EVER RE-ENCOUNTERED.
…
It's comforting to have this knowledge.
All those involved with the vaccines lied their tails off, because they knew billions in revenue was on the way. They also knew the vax were neither safe or effective, but the money was too great an incentive.
Natural immunity is lifelong as that is the nature of evolution. The critical part is what chemical was introduced in the months prior in that environmental setting that resulted in the influenza strain to mutate and spread, reaching outbreak point. With influenzas timing there were various changes to artificial fertilisers and that food was then provided to military personal which is where the outbreaks first manifest. Bacteria and Viruses are not enemies their friends trying to explain that the environment, and thus human consumption potential, has been altered and the mutation that presents as human illness is making adjustments to our system so the responsible chemical doesn't kill us. When the mutation is too vast a difference, acute and instant exposure, then it is "speaking in a language our cells can't understand and so it is deadly. When it is a slighter alteration, like from sub-acute exposure then it presents as a sickness. This is why we have over 3000 strains of beneficial e.coli in our gut and don't get sick from it yet a mutagenic e.coli say that's been exposed to Cadmium will result in e.coli poisoning. The e.coli is protecting the human system through illness so that we quickly excrete and the chemical doesn't cause even greater harms once absorbed.
Wow Wow wow!
https://theparalleluniverse.substack.com/p/faucis-knockout-punch?publication_id=1202385&utm_campaign=email-post-title&r=pf0t8
I saw a study way back after the beginning of COVID that said the same thing.
They injected soldiers with a virus there was no Spanish Flu no virus has ever been isolated !!! No such thing as Covid !! They Tortured and Murdered my Father with a Fake PCR TEST AND DRUGGED HIM WITH REMDESIVIR AND A VENTILATOR UNTIL HIS ORGANS FAILED THEN TRIED TO KILL HIM WITH MORPHINE BUT HE WOKE UP SO THEN THEY USED FENTANYL NOT SOME FAKE VIRUS !!!!!
Sorry, not buying into the current state of virology, viruses and virologists. It's all poppycock.
They lied? Be still my beating heart.
Big Pharma is brainwashing people to be Natural Immunity Deniers.
Viruses don't exist, Dr.Alexander. Have you been paying attention? Stop helping PHARMA Gaslight humanity!
Good to know. Thank you, Dr Alexander.
Question....whatever immunity was provided by the shots did not last long because the virus mutated into different strains. What is the difference with natural immunity that makes it life long? Or is natural immunity only effective against the strain it was created against?