Immunization of mice by Hollow Mesoporous Silica Nanoparticles as carriers of Porcine Circovirus Type 2 ORF2 Protein

被引:70
作者
Guo, Hui-Chen [1 ,2 ]
Feng, Xiao-Ming [1 ,2 ]
Sun, Shi-Qi [1 ,2 ]
Wei, Yan-Quan [1 ,2 ]
Sun, De-Hui [1 ,2 ]
Liu, Xiang-Tao [1 ,2 ]
Liu, Zai-Xin [1 ,2 ]
Luo, Jian-Xiong [1 ,2 ]
Yin, Hong [1 ,2 ]
机构
[1] Chinese Acad Agr Sci, State Key Lab Vet Etiol Biol, Lanzhou Vet Res Inst, Lanzhou 730046, Gansu, Peoples R China
[2] Chinese Acad Agr Sci, Natl Foot & Mouth Dis Reference Lab, Lanzhou Vet Res Inst, Lanzhou 730046, Gansu, Peoples R China
基金
中国国家自然科学基金;
关键词
Hollow mesoporous silica nanoparticles (HMSNs); Porcine circovirus type 2 (PCV2): ORF2; Delivery; Immunization; Mice; MULTISYSTEMIC WASTING SYNDROME; MAJOR CAPSID PROTEIN; DRUG-DELIVERY; FUNCTIONAL DIVERSITY; PCV2; IDENTIFICATION; VACCINATION; REPLICATION; PROTECTION; ANTIBODY;
D O I
10.1186/1743-422X-9-108
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Backgroud: Porcine circovirus type 2 (PCV2) is a primary etiological agent of post-weaning multi-systemic wasting syndrome (PMWS), which is a disease of increasing importance to the pig industry worldwide. Hollow mesoporous silica nanoparticles (HMSNs) have gained increasing interest for use in vaccines. Methods: To study the potential of HMSNs for use as a protein delivery system or vaccine carriers. HMSNs were synthesized by a sol-gel/emulsion(oil-in-water/ethanol) method, purified PCV2 GST-ORF2-E protein was loaded into HMSNs, and the resulting HMSN/protein mixture was injected into mice. The uptake and release profiles of protein by HMSNs in vitro were investigated. PCV2 GST-ORF2-E specific antibodies and secretion of IFN-gamma were detected by enzyme-linked immunosorbent assays, spleen lymphocyte proliferation was measured by the MTS method, and the percentage of CD4+ and CD8+ were determined by flow cytometry. Results: HMSNs were found to yield better binding capacities and delivery profiles of proteins; the specific immune response induced by PCV2 GST-ORF2-E was maintained for a relatively long period of time after immunization with the HMSN/protein complex. Conclusion: The findings suggest that HMSNs are good protein carriers and have high potential for use in future applications in therapeutic drug delivery.
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页数:10
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