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demonstrate that PLGA nanoparticles encapsulating recombinant human myelin basic protein (MBP) significantly ameliorate EAE severity and neuroinflammation, supporting MBP as a viable tolerogenic cargo beyond MOG-based models

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The trajectory appeared similar across types of weight-loss medication

Abstract Aims/hypothesis Our aim was to assess treatment discontinuation, reinitiation and switching between drugs within the same drug class for glucagon-like peptide-1 (GLP-1) receptor agonists and sodium-glucose cotransporter 2 (SGLT2) inhibitors in individuals with type 2 diabetes