化学
免疫系统
硒
体内
下调和上调
吞噬作用
受体
多糖
体外
生物化学
细胞因子
分子生物学
细胞生物学
分泌物
白细胞介素
药理学
PLGA公司
CD40
基因表达
作者
Chunyan Chen,Guilan Fan,Yi Lin,Zijie Zheng,Xueli Zhang,Yuqi Zhang,Tao Qin,Zhe Ren,Chunyan Chen,Guilan Fan,Yi Lin,Zijie Zheng,Xueli Zhang,Yuqi Zhang,Tao Qin,Zhe Ren
标识
DOI:10.1002/cbdv.202501322
摘要
ABSTRACT In this study, a nano‐drug delivery system based on poly(lactic‐co‐glycolic acid) (PLGA) that modified selenated Myricaria germanica polysaccharide (sMGP) was developed to enhance immune responses. At the O to W1 ratio of 8.29, the W2 to primary emulsion ratio of 7.62, and the concentration of PLGA was 37.94 mg/mL, the entrapment efficiency of sMGP‐PLGA was 90.27%. In vitro, at the concentration of 3.125–25 µg/mL, sMGP‐PLGA significantly enhanced the phagocytosis of RAW264.7 macrophages, facilitated the upregulation of surface molecules CD40 and CD86, and increased the secretion of cytokines interferon‐gamma (IFN‐γ) and interleukin (IL)‐4, as well as the gene expression levels of toll‐like receptor 4 and nuclear factor kappa B. In vivo sMGP‐PLGA significantly increased the Newcastle disease antibodies, IFN‐γ, and IL‐6 levels, activated the immune functionality of spleen, thymus, and bursa of Fabricius, and improved the organ index. Meanwhile, sMGP‐PLGA promoted the proliferation of T and B lymphocytes. These findings indicate that sMGP‐PLGA could enhance the immune activity.
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