So first of all, let’s just talk theoretically. If you get a flu shot, there’s a number of dead or weak flu viruses that are injected into your arm. They stay there. Your body circulates, your immune system recognises them, develops antibodies, develops B cells and T cells to that. They stay there and you develop an immunity. When you catch the flu, it comes into your nose and it is trapped in your nasal mucosa. Your immune system encounters the virus in the nasal mucosa where there are various mechanisms for it to stay for a while while you develop antibodies and you develop B cells and T cells.
We have never in the past had a situation where our immune systems are confronted with a spike protein suddenly appearing in the blood at any and all parts of the body. So, theoretically, because it is such a totally different procedure, it should be properly tested before it is proclaimed to be either effective or safe. The next thing we don’t know is – comparing it again to the flu vaccine – how much of the dead material or the attenuated virus goes into your body.
With these messenger RNA portions telling yourselves to make spike protein; I don’t know – and I don’t think anybody who knows has ever said it – but certainly it is not known how much of the spike it is produced. And [whether] it is the same in all people. Do some people produce so much spike protein and other people produce so much depending on how their cells respond? And nor do we know for how long; does it just make it once – so there’s just one production of spike protein and then it’s the end? Or does it keep on for an hour or a day or for ten days or for two months?
So the amount of spike protein that is generated is uncontrollable, it’s unknown. The duration of time over which it will be generated and also where in your body it will be produced [is also unknown]. So these are such importantly different variables compared to the localised inoculation which is controlled that it is, to me, reckless to use that in humans until you have properly proven in animals that you know what you’re doing and it’s effective and safe.
So those are the reasons why theoretically I would be worried about this vaccination. However, [also] excited, because if it works – it would be an amazing scientific breakthrough that would be good for humanity and could possibly be used in many other things and infection, such as cancer or other diseases. So, it’s a very interesting scientific breakthrough. But the effects of it are not known.
Now, normally vaccines and other new drugs or whatever get tested in animals before it gets tested in humans. What we are told is that in the case of this all previous attempts at developing mRNA vaccinations for coronavirus in animals, not SARS-CoV-2, previous attempts have all failed.
So the animal trials have never succeeded. Also in this – in the Covid-19, SARS-CoV-2 – the animal trials failed. And the reason that we are told by virologists or immunologists why they failed is because of immunosuppression and because of another phenomenon called antibody dependent enhancement. -
Dr Herman Edeling