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Neither approach resolves the deeper problem: People are already injecting drugs that scientists have not adequately studied

The development of HBsAg-HBIG IC as a therapeutic vaccine for CHB was based on the concept that the Fc fragment of antibodies in the IC could interact with Fc receptors on DCs cells, and initiate more effective immune responses in hosts

These peptides have NEVER been approved, so there's no "label" to go off of

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In microbial infections, more pathogenic mechanisms have been described