Gigaohm Biological (16 March)
At 01:47 Jonathan discusses whether the JNJ/AZ transformation and hepatitis are Connected. Johnson & Johnson (JnJ) and Astra Zeneca (Az) “vaccines” were made with a monkey adenovirus shell. Basically they took out the insides and put their mRNA instructions inside. All humans (and many animals) carry adenoviruses, often in their gut and they are harmless. The adenovirus has been linked with the increase in hepatitis and liver failure in children. JC does not believe that JnJ and Az deattenuated (recombination with wild virus) J.C. believes that is more likely that your immune response is directed at the adenovirus monkey shell as well as the spike-protein. In other words evolutionary pressure is put on the relatively “benign” adenovirus monkey shell. A new niche created for adenovirus? Below is a hypothesis that argues for deattenuation. And riddle me this, riddle me that…why are we seeing a rise in cases of monkey pox?
Maybe they have a better reason for restricting J&J?
Did their attenuated/nonreplicating adenovirus recombine with a wild adenovirus to start causing a new form of viral hepatitis in kids?
We have a great deal to talk about tomorrow night.
Biology: Get Some.
— 🔬 ))ay( 🚴 (@jjcouey) May 16, 2022
And the connection grows stronger
They found Hadv-4 in the hepatitis cases, which belongs to human type F (Hadv-F)
And what are Hadv-F close to – monkey adeno !
More closer than other human adeno
Even the AZ adeno (Y25) has a lot of homology https://t.co/oXOlb0N5On
— sandeep chakraborty (@sanchak74) May 4, 2022
It seems obvious this is a deattenuation event. Either they are picking up kids who are cross reacting Y25<->hAdV41 … or… their test for hAdV41 is actually detecting a deattenuated Y25
And they don’t have a clue.
— Jikkyleaks (Fan account) 🐭 (@Jikkyleaks) May 4, 2022
Wonder where it’s coming from 🤔🤔🤔 pic.twitter.com/zorzm5GrHL
— Kat😺🏴🇬🇧 (@Kat1022_) May 16, 2022