Chitosan, hydroxypropyltrimethyl ammonium chloride chitosan and sulfated chitosan nanoparticles as adjuvants for inactivated Newcastle disease vaccine

被引:54
作者
Yang, Yue [1 ,2 ,3 ]
Xing, Ronge [1 ,2 ]
Liu, Song [1 ,2 ]
Qin, Yukun [1 ,2 ]
Li, Kecheng [1 ,2 ]
Yu, Huahua [1 ,2 ]
Li, Pengcheng [1 ,2 ]
机构
[1] Chinese Acad Sci, Key Lab Expt Marine Biol, Ctr Ocean Mega Sci, Inst Oceanol, 7 Nanhai Rd, Qingdao 266071, Shandong, Peoples R China
[2] Qingdao Natl Lab Marine Sci & Technol, Lab Marine Drugs & Bioprod, 1 Wenhai Rd, Qingdao 266237, Shandong, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
国家重点研发计划;
关键词
Newcastle disease virus; Adjuvant; Nanoparticle; Chitosan; Hydroxypropyltrimethyl ammonium chloride chitosan; Sulfated chitosan; ASTRAGALUS POLYSACCHARIDE; INTRANASAL VACCINATION; IMMUNE-RESPONSE; DELIVERY; MUCOSAL; ENHANCE; MICROPARTICLES; IMMUNIZATION; MACROPHAGES; VETERINARY;
D O I
10.1016/j.carbpol.2019.115423
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Chitosan (CS) and its water-soluble derivatives, hydroxypropyltrimethyl ammonium chloride chitosan (HACC) and sulfated chitosan (SCS), were used as adjuvants of inactivated Newcastle disease (ND) vaccine. First, NDV-loaded and blank CS, HACC/CS and SCS nanoparticles were prepared. The particle sizes were respectively 343.43 +/- 4.12, 320.03 +/- 0.84, 156.2 +/- 9.29 nm and the zeta potentials were respectively +19.67 +/- 0.58, +18.3 +/- 0.5, -17.8 +/- 2.65 mV under the optimal conditions. Then chickens were immunized with nanoparticles or commercial inactivated oil emulsion vaccine. After immunization, the humoral immunity levels of the chickens were evaluated. The cellular immunity levels were determined by the quantification of cytokines, lymphocyte proliferation assay, the percentages of CD4(+) and CD8(+) T lymphocytes. Finally, the chickens were challenged with highly virulent virus. The results demonstrated that the humoral immunity levels in NDV-loaded CS and HACC/CS nanoparticles groups were lower than commercial vaccine but the cellular immunity levels are better. Moreover, the prevention effects of NDV-loaded CS and HACC/CS nanoparticles against highly virulent NDV are comparable to commercial vaccine. Our study provides the basis of developing HACC and CS as effective vaccine adjuvants.
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页数:9
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