"The current intramuscular vaccines are designed to elicit systemic immunity
➡️ without conferring mucosal immunity in the nasal compartment, which is the first barrier that SARS-CoV-2 virus breaches before dissemination to the lung."
"Mucosal vaccination can stimulate both systemic and mucosal immunity and has the advantage of being a non-invasive procedure suitable for immunization of large populations."
"Although the COVID-19 pandemic has been ongoing now for several months, very little attention has been given to mucosal immunity in SARS-CoV-2 infection. Yet this virus primarily infects the mucosal surfaces of the respiratory tract"
"Almost all efforts at vaccine development against COVID-19 focus on systemic injection, which predominantly induces circulatory IgG antibodies and, potentially, cytotoxic T cells (18)."
"the intranasal administration of a vaccine is inherently associated with an IgA response. An additional benefit of IgA is based on its non-inflammatory effects"
"the intranasal route was superior to the IM route in terms of a systemic and local humoral response, and both had a stronger systemic and pulmonary CTL response"
"Sterilizing immunity requires neutralizing antibodies at the site of infection, which for respiratory viruses such as SARS-CoV-2 implies the occurrence of neutralizing IgA in mucosal secretions.
"Vaccines that are injected into the muscle – i.e., the interior of the body – will only induce IgG and circulating IgA, not secretory IgA. Such antibodies cannot and will not effectively protect the mucous membranes from infection by SARS-CoV-2."
You can also learn a lot just from listening to this video;
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For my Norwegian followers;
Jan Raa, professor emeritus i mikrobiologi. Forskningsdirektør i offentlige FoU-institutter og i private biomedisinske bedrifter. Har ledet utvikling av fiskevaksiner i Norge.
"This study was able to determine that multiciliated cells in the nasal epithelium are the first cells that are targeted in the early COVID-19 infection."
"This implies that targeting these cells using specific treatments, such as through nasal sprays, can be an ideal strategy to curb COVID-19 infection in the early stages."
Some say that there was no pandemic (they are right), but there certainly was an attempt to create one.
Some say that there was no SARS-COVID-19 virus, that were it not for the RT-PCR tests no one would have noticed the "pandemic". That they just rebranded the common flu, after all, where did it go in 2020/21?
In this 🧵 I will attempt to explain what I believe happened based on all the data I have collected, some of which I will present here.
The reason the pandemic failed is connected to the reason the vaccine also failed. In fact, it seems the vaccine was ready before the virus release/emergence.
Just listen to Stéphane Bancel, the CEO of Moderna;
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SARS-CoV-2 was created by the EcoHealth Alliance at the Wuhan Institute of Virology, coordinated by Peter Daszak @PeterDaszak
Any virus will bypass even the best facemasks through the nasolacrimal duct (also called the tear duct).
Your tears clean your eyes from dust, pollen, and viruses, which are then drained into your nose.
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Any droplet of infected fluid that lands on your facemask are turned into tiny aerosol particles as you inhale, and gets deep into your lungs, increasing the chances of getting infected. In other words, masks make things worse.
Why the vaccines cannot protect against infection by respiratory viruses: ⬇️
➡️ A fundamental mistake underlying the development of the COVID-19 vaccines was to neglect the functional distinction between the two major categories of antibodies that the body produces...
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...in order to protect itself from pathogenic microbes.
➡️ The first category (secretory IgA) is produced by immune cells (lymphocytes) which are located
directly underneath the mucous membranes that line the respiratory and intestinal tract.
The antibodies produced by...
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...these lymphocytes are secreted through and to the surface of the mucous membranes. These antibodies are thus on-site to meet air-borne viruses, and they may be able to prevent viral binding and infection of the cells.
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