We locked children down too long & hard & denied their IMMUNE system training (innate antibodies/immune system) needed); 'Adeno-associated virus 2 infection in children with non-A-E hepatitis'

by Paul Alexander

Lockdowns did this, prevented them from training immune system, Collins, Fauci & Birx & Walensky, such stupid inane a vapid health idiots, dangerous; they caused this dangerous dual adeno & hepatitis

Parents, pay attention please:

By locking children down and closing schools the insane way we did, we prevented children from sharing virus among themselves, infecting each other, and taxing and toning and tuning up their developing immune systems. This study is clearly showing us what happens due to the lockdowns.

The vast majority of these afflicted children are under 5 years old. Detected in plasma of all the sample, 9 out of 9 children, the adeno-associated virus. We see small sample size but the clarity of the data and the completeness is staggering. Though we still be cautious in the non-peer reviewed status at this time.

Fauci and Birx et al. caused this hepatitis devastation. They prevented the immune system of children the proper development at the proper time (window of opportunity) due to their lockdown lunacy and we are now seeing the impact and will see more, especially if we vaccinate with the COVID vaccine.

Due to post lockdowns, it is likely that children are now being devastated with two common viruses spreading among children e.g. Acute non-A-E paediatric hepatitis and adeno-associated virus 2 (AAV2).

Key phrases:

“Acute non-A-E paediatric hepatitis is associated with the presence of AAV2 infection, which could represent a primary pathogen or a useful biomarker of recent HAdV or HHV6B infection.”

“AAV2 typically requires a coinfecting ‘helper’ virus to replicate.” It needs another virus to co-infect, needs a ‘helper’ virus such as another adeno virus or a herpetic virus. You need to be unfortunate to be impacted by both at the same time.

“Adeno-associated virus 2 (AAV2), was detected in the plasma of 9/9 and liver of 4/4 patients but in 0/13 sera/plasma of age-matched healthy controls, 0/12 children with adenovirus (HAdV) infection and normal liver function and 0/33 children admitted to hospital with hepatitis of other aetiology.”

We all are exposed to these adeno viruses. Yet children subjected to lock downs and school closures and repeated, were thus exposed to these viruses (adeno etc.) later in life and likely did not develop immunity (the robust immune system) as they normally should e.g. the lockdowns, and now paying a price as the immunity has not been built up and many of these children now need liver transplants, catastrophic. Many of these children need liver transplantations which is very devastation at such an age. Will need life-long support. This acute hepatitis is devastating.

Similarly, if we vaccinate with the COVID vaccine, the vaccinal antibodies will subvert the innate antibodies in children from training by their binding to live viruses, pathogen in the environment. The vaccinal antibodies will now block the innate antibodies from binding and training and thus educating the innate immune system to cope with a broad range of viruses e.g. glycosylated viruses.

The lockdown and school closures caused this, NOT COVID, not the vaccine. But now we will do to children same with the vaccine. We will damage their immune system.

“An outbreak of acute hepatitis of unknown aetiology in children was first reported in Scotland in April 2022.1 Cases aged <16 years have since been identified in 35 countries.2 Here we report a detailed investigation of 9 early cases and 58 control subjects. Using next-generation sequencing and real-time PCR, adeno-associated virus 2 (AAV2), was detected in the plasma of 9/9 and liver of 4/4 patients but in 0/13 sera/plasma of age-matched healthy controls, 0/12 children with adenovirus (HAdV) infection and normal liver function and 0/33 children admitted to hospital with hepatitis of other aetiology.”

SOURCE:

Adeno-associated virus 2 infection in children with non-A-E hepatitis