Collectively, these biomaterial-based therapies deliver payloads to induce durable antigen-specific tolerance while minimizing systemic side effects
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It enhances glucose-dependent insulin secretion, inhibits glucagon release, slows gastric emptying, and suppresses appetite via central nervous system pathways (Milder et al
GLP-1 agonism is a mechanism of action typically not used by these drugs, and in the context of Eriomin, it appears to be a relatively safe mechanism, as no significant adverse effects were reported in this study or the other clinical study
The cell then exports the spike protein to the cell membrane