赛马鲁肽
免疫系统
免疫原性
兴奋剂
胰高血糖素样肽1受体
接种疫苗
免疫学
医学
受体
2型糖尿病
糖尿病
内科学
内分泌学
利拉鲁肽
作者
Gustav van Niekerk,Lotte Coelmont,Yeranddy A. Alpízar,Lara Kelchtermans,Elias Broeckhoven,Kai Dallmeier
标识
DOI:10.1016/j.cytogfr.2024.07.006
摘要
Glucagon-like peptide-1 receptor agonists (GLP-1RAs), such as semaglutide (Ozempic®), have emerged as effective treatments for diabetes and weight management. However, recent evidence indicates that GLP-1R signalling influences various tissues, including the immune system. Notably, GLP-1 has a short half-life (< 5 minutes) and exists in the picomolar range, while GLP-1RAs like semaglutide have extended half-lives of several days and are administered at supraphysiological doses. This review explores the potential impact of these medications on vaccine efficacy. We examine evidence suggesting that GLP-1RAs may attenuate vaccine responses through direct effects on immune cells and modulation of other tissues. Additionally, we discuss how GLP-1R signalling may create a tolerogenic environment, potentially reducing vaccine immunogenicity. Given the widespread use of GLP-1RAs, it is crucial to understand their impact on immune responses and the translational implications for vaccination outcomes.
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