Laboratory of Molecular Immunology, Department of Microbiology, Faculty of Biological Sciences, University of Concepción, Concepción, Chile.
Biomed Res Int. 2017;2017:6535479. doi: 10.1155/2017/6535479. Epub 2017 Sep 7.
As an alternative brucellosis prevention method, we evaluated the immunogenicity induced by new multivalent DNA vaccines in BALB/c mice. We constructed the vaccines by fusion of BAB1_0273 and/or BAB1_0278 open reading frames (ORFs) from genomic island 3 (GI-3) and the 2308 gene with a link based on prolines and alanines (pV273-, pV278- and pV273-278-, resp.). Results show that immunization with all tested multivalent DNA vaccines induced a specific humoral and cellular immune response. These novel multivalent vaccines significantly increased the production of IgM, IgG, and IgG2a antibodies as well as IFN- levels and the lymphoproliferative response of splenocytes. Although immunization with these multivalent vaccines induced a typical T-helper 1- (Th1-) dominated immune response, such immunogenicity conferred low protection levels in mice challenged with the 2308 pathogenic strain. Our results demonstrated that the expression of BAB1_0273 and/or BABl_0278 antigens conjugated to SOD protein can polarize mice immunity to a Th1-type phenotype, conferring low levels of protection.
作为布鲁氏菌病的一种替代预防方法,我们评估了新的多价 DNA 疫苗在 BALB/c 小鼠中诱导的免疫原性。我们通过融合基因组岛 3(GI-3)中的 BAB1_0273 和/或 BAB1_0278 开放阅读框(ORF)和基于脯氨酸和丙氨酸的链接(pV273-、pV278-和 pV273-278-,分别)构建了这些疫苗。结果表明,用所有测试的多价 DNA 疫苗免疫均可诱导特异性体液和细胞免疫应答。这些新型多价疫苗显著增加了 IgM、IgG 和 IgG2a 抗体的产生以及 IFN-水平和脾细胞的淋巴增殖反应。尽管这些多价疫苗免疫诱导了典型的辅助性 T 细胞 1(Th1-)优势免疫应答,但这种免疫原性在 2308 致病性菌株攻毒的小鼠中赋予了低水平的保护。我们的结果表明,与 SOD 蛋白偶联的 BAB1_0273 和/或 BABl_0278 抗原的表达可以使小鼠的免疫偏向 Th1 表型,赋予低水平的保护。