Monoclonal antibodies for 'covid'

another important reason to establish that viruses don't exist

From wiki; ‘Sotrovimab's development began in December 2019, at Vir Biotechnology when Vir scientists first learned of the initial COVID-19 outbreak in China.[17] Vir subsidiary Humabs BioMed had already compiled a library of frozen blood samples from patients infected with viral diseases, including two samples from patients infected with SARS-CoV-1.[17] Vir scientists obtained samples of the novel SARS-CoV-2 virus and mixed them with various antibodies recovered from the old SARS-CoV-1 blood samples.[17] The objective was to identify antibodies effective against both SARS-CoV-1 and SARS-CoV-2.[17] This would imply that the antibodies were targeting highly conserved sequences and in turn would be more likely to remain effective against future variants of SARS-CoV-2.[17] In April 2020, Lawrence Berkeley National Laboratory conducted a X-ray crystallography study at Vir's request to investigate how such antibodies bind to SARS-CoV-2 at the molecular level.[17] The Berkeley Lab data helped Vir identify candidates for further study, and Vir eventually settled on a single candidate antibody, S309.[17] Vir collaborated with GlaxoSmithKline to make various refinements to S309, resulting in sotrovimab.[17]

Sotrovimab has been engineered to possess an Fc LS mutation (M428L/N434S) that confers enhanced binding to the neonatal Fc receptor[18] resulting in an extended half-life and potentially enhanced drug distribution to the lungs .’

In other words;

Scientists added stressed cell cultures (‘viruses’) to samples of people experiencing symptoms of detox. Some of the sticky globulins (antibodies) in the samples stuck to some of the proteins in the cell culture. The proteins that caused the most binding reaction where determined to be the viral antigens.

They put these proteins/ viral antigens into an animal, usually a mouse or a hamster, who produced antibody producing B cells. The B cells were fused with a myeloma and the antibodies continued to produced from these ‘immortal’ cells in culture.

The antibodies bind to and block the viral antigens.

However, the viral antigens are in fact cellular proteins which are involved in the detox and healing process. Thus the healing process is suppressed. Explaining the very small improvement allegedly seen in symptoms, but also the illness and damage that monoclonal antibodies produce; which may soon start to rival the adverse events of vaccines.

Not to mention the continued abuse and torture of animals in labs, all of which is solely for profit, unnecessary and barbaric.

Jo

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