The observed sharp overexpression of cytotoxic genes in peripheral T cells and innate-like lymphocytes in patients, but not in immunised participants, was probably caused by increased interferon signalling.
The research further states that “Analysis of B and T cell receptor repertoires revealed that while the majority of clonal B and T cells in COVID-19 patients were effector cells, in vaccine recipients clonally expanded cells were primarily circulating memory cells.”
Simply put, this indicates that although memory response necessitates a slower-responding adaptive mode, effector cells initiate a faster and more robust innate response.
Whereas the vaccination primarily promotes adaptive immunity, natural immunity communicates much more innate immunity.
Last year, the media misled people into believing that a decline in antibody levels indicated a deterioration in immunity, which is exactly.
What is happening with today’s vaccinations. However, Nature said, “People who recover [even] from mild COVID-19 have bone-marrow cells that can churn out antibodies for decades.”
