首页> 外文OA文献 >Dendritic Cell Targeting of Bovine Viral Diarrhea Virus E2 Protein Expressed by Lactobacillus casei Effectively Induces Antigen-Specific Immune Responses via Oral Vaccination
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Dendritic Cell Targeting of Bovine Viral Diarrhea Virus E2 Protein Expressed by Lactobacillus casei Effectively Induces Antigen-Specific Immune Responses via Oral Vaccination

机译:由乳酸杆菌表达的牛病毒腹泻病毒E2蛋白的树突状细胞靶向通过口腔疫苗接种有效地诱导抗原特异性免疫应答

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摘要

Bovine viral diarrhea caused by bovine viral diarrhea virus (BVDV) is an important disease in cattle, resulting in significant economic losses to the cattle industry worldwide. In order to develop an effective vaccine against BVDV infection, we constructed a dendritic cell (DC)-targeting oral probiotic vaccine (pPG-E2-DCpep/LC W56) using Lactobacillus casei as antigen delivery carrier to express BVDV glycoprotein E2 fused with DC-targeting peptide, and the immunogenicity of orally administered probiotic vaccine was evaluated in mice model. Our results showed that after immunization with the probiotic vaccine, significantly levels of antigen-specific sera IgG and mucosal sIgA antibodies (p < 0.05) with BVDV-neutralizing activity were induced in vivo. Challenge experiment showed that pPG-E2-DCpep/LC W56 can provide effective immune protection against BVDV, and BVDV could be effectively cleared from the intestine of immunized mice post-challenge. Moreover, the pPG-E2-DCpep/LC W56 could efficiently activate DCs in the intestinal Peyer’s patches, and significantly levels of lymphoproliferative responses, Th1-associated IFN-γ, and Th2-associated IL-4 were observed in mice immunized with pPG-E2-DCpep/LC W56 (p < 0.01). Our results clearly demonstrate that the probiotic vaccine could efficiently induce anti-BVDV mucosal, humoral, and cellular immune responses via oral immunization, indicating a promising strategy for the development of oral vaccine against BVDV.
机译:由牛病毒腹泻病毒(BVDV)引起的牛病毒性腹泻是牛中的重要疾病,导致全球牛行业的显着经济损失。为了对BVDV感染进行有效的疫苗,我们构建了使用乳杆菌酪蛋白作为抗原递送载体的树突细胞(DC)的口腔益生菌疫苗(PPG-E2-DCPEP / LC W56),以表达与DC-融合的BVDV糖蛋白E2在小鼠模型中评价靶向肽,以及口服给药益生菌疫苗的免疫原性。我们的研究结果表明,在对益生菌疫苗免疫后,在体内诱导具有BVDV中和活性的抗原特异性血清IgG和粘膜SIGA抗体(P <0.05)的显着水平。挑战实验表明,PPG-E2-DCPEP / LC W56可以为BVDV提供有效的免疫保护,并且可以从攻击后免疫小鼠的肠道有效地清除BVDV。此外,PPG-E2-DCPEP / LC W56可以有效地激活肠道Peyer的贴片中的DC,并且在用PPG免疫的小鼠中观察到淋巴抑制反应,Th1相关的IFN-γ和Th2相关的IL-4的显着水平E2-DCPEP / LC W56(P <0.01)。我们的结果清楚地表明,益生菌疫苗可以通过口服免疫有效地诱导抗BVDV粘膜,体液和细胞免疫应答,表明对BVDV的口腔疫苗发育的有希望的策略。

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