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Picrasidine S Induces cGAS-Mediated Cellular Immune Response as a Novel Vaccine Adjuvant.

Xiaofan DingMengxue SunFusheng GuoXinmin QianHaoyu YuanWenjiao LouQixuan WangXiaoguang LeiWenwen Zeng
Published in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2024)
New adjuvants that trigger cellular immune responses are urgently needed for the effective development of cancer and virus vaccines. Motivated by recent discoveries that show activation of type I interferon (IFN-I) signaling boosts T cell immunity, this study proposes that targeting this pathway can be a strategic approach to identify novel vaccine adjuvants. Consequently, a comprehensive chemical screening of 6,800 small molecules is performed, which results in the discovery of the natural compound picrasidine S (PS) as an IFN-I inducer. Further analysis reveals that PS acts as a powerful adjuvant, significantly enhancing both humoral and cellular immune responses. At the molecular level, PS initiates the activation of the cGAS-IFN-I pathway, leading to an enhanced T cell response. PS vaccination notably increases the population of CD8+ central memory (T CM )-like cells and boosts the CD8+ T cell-mediated anti-tumor immune response. Thus, this study identifies PS as a promising candidate for developing vaccine adjuvants in cancer prevention.
Keyphrases
  • immune response
  • dendritic cells
  • toll like receptor
  • papillary thyroid
  • early stage
  • squamous cell
  • small molecule
  • gene expression
  • genome wide
  • working memory
  • single cell
  • lymph node metastasis
  • inflammatory response