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Adjuvants modulating mucosal immune responses or directing systemic responses towards the mucosa

机译:佐剂调节粘膜免疫反应或将全身反应引导至粘膜

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摘要

In developing veterinary mucosal vaccines and vaccination strategies, mucosal adjuvants are one of the key players for inducing protective immune responses. Most of the mucosal adjuvants seem to exert their effect via binding to a receptor/or target cells and these properties were used to classify the mucosal adjuvants reviewed in the present paper: (1) ganglioside receptor-binding toxins (cholera toxin, LT enterotoxin, their B subunits and mutants); (2) surface immunoglobulin binding complex CTA1-DD; (3) TLR4 binding lipopolysaccharide; (4) TLR2-binding muramyl dipeptide; (5) Mannose receptor-binding mannan; (6) Dectin-1-binding ss 1,3/1,6 glucans; (7) TLR9-binding CpG-oligodeoxynucleotides; (8) Cytokines and chemokines; (9) Antigen-presenting cell targeting ISCOMATRIX and ISCOM. In addition, attention is given to two adjuvants able to prime the mucosal immune system following a systemic immunization, namely 1alpha, 25(OH)2D3 and cholera toxin.
机译:在开发兽用粘膜疫苗和疫苗接种策略中,粘膜佐剂是诱导保护性免疫反应的关键因素之一。大多数黏膜佐剂似乎是通过与受体/或靶细胞结合而发挥作用,这些特性被用于对黏膜佐剂进行分类:(1)神经节苷脂受体结合毒素(霍乱毒素,LT肠毒素,其B亚基和突变体); (2)表面免疫球蛋白结合复合物CTA1-DD; (3)TLR4结合脂多糖; (4)TLR2结合的鼠基二肽; (5)结合甘露糖受体的甘露聚糖; (6)Dectin-1-binding ss 1,3 / 1,6葡聚糖; (7)TLR9-结合的CpG-寡脱氧核苷酸; (八)细胞因子和趋化因子; (9)靶向抗原呈递细胞的ISCOMATRIX和ISCOM。另外,注意了在全身性免疫后能够引发粘膜免疫系统的两种佐剂,即1alpha,25(OH)2D3和霍乱毒素。

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