Cistanche deserticola polysaccharide- functionalized dendritic fibrous nano-silica −based adjuvant for H9N2 oral vaccine enhance systemic and mucosal immunity in chickens

佐剂 粘膜免疫 多糖 化学 疫苗佐剂 免疫 免疫系统 纳米- 免疫学 医学 材料科学 生物化学 复合材料
作者
Jin He,Xuanqi Lu,Ningning Mao,Tianyu Zhu,Lin Yu,Yaming Yu,Peng Song,Xiangwen Deng,Bing Hu,Wenming Jiang,Yu Lu,Deyun Wang,Deyun Wang
出处
期刊:International Journal of Pharmaceutics [Elsevier BV]
卷期号:660: 124318-124318 被引量:9
标识
DOI:10.1016/j.ijpharm.2024.124318
摘要

Avian influenza virus subtype H9N2 has the ability to infect birds and humans, further causing significant losses to the poultry industry and even posing a great threat to human health. Oral vaccine received particular interest for preventing majority infection due to its ability to elicit both mucosal and systemic immune responses, but their development is limited by the bad gastrointestinal (GI) environment, compact epithelium and mucus barrier, and the lack of effective mucosal adjuvants. Herein, we developed the dendritic fibrous nano-silica (DFNS) grafted with Cistanche deserticola polysaccharide (CDP) nanoparticles (CDP-DFNS) as an adjuvant for H9N2 vaccine. Encouragingly, CDP-DFNS facilitated the proliferation of T and B cells, and further induced the activation of T lymphocytes in vitro. Moreover, CDP-DFNS/H9N2 significantly promoted the antigen-specific antibodies levels in serum and intestinal mucosal of chickens, indicating the good ability to elicit both systemic and mucosal immunity. Additional, CDP-DFNS facilitate the activation of CD4 + and CD8 + T cells both in spleen and intestinal mucosal, and the indexes of immune organs. This study suggested that CDP-DFNS may be a new avenue for development of oral vaccine against pathogens that are transmitted via mucosal route.
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