Umthong Supawadee, Buaklin Arun, Jacquet Alain, Sangjun Noppadol, Kerdkaew Ruthairat, Patarakul Kanitha, Palaga Tanapat
Interdisciplinary Program in Medical Microbiology, Graduate School, Chulalongkorn University, Bangkok 10330, Thailand.
Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand.
J Microbiol Biotechnol. 2015 Apr;25(4):526-36. doi: 10.4014/jmb.1408.08007.
Leptospirosis is a worldwide zoonotic disease caused by pathogenic Leptospira, a genus of which more than 250 serovars have been identified. Commercial bacterin vaccines are limited in that they lack both cross-protection against heterologous serovars and long-term protection. This study investigated in mice the immunogenicity of an anti-leptospirosis vaccine, using the outer membrane proteins LipL32 and Loa22 as antigens. The immunogenicity of this vaccine formulation was compared with those induced by vaccines based on LipL32 or Loa22 alone. A DNA-encapsulated chitosan nanoparticle was used for in vivo DNA delivery. Using a unique DNA plasmid expressing both lipL32 and loa22 for vaccination, higher antibody responses were induced than when combining plasmids harboring each gene separately. Therefore, this formulation was used to test the immunogenicity when administered by a heterologous prime (DNA)-boost (protein) immunization regimen. The specific antibody responses against LipL32 (total IgG and IgG1) and Loa22 (IgG1) were higher in mice receiving two antigens in combination than in those vaccinated with a single antigen alone. Although no significant difference in splenic CD4+ T cell proliferation was observed among all groups of vaccinated mice, splenocytes from mice vaccinated with two antigens exhibited higher interferon-γ and IL-2 production than when using single antigens alone upon in vitro restimulation. Taken together, the immunogenicity induced by LipL32 and Loa22 antigens in a heterologous primeboost immunization regimen using chitosan as a DNA delivery system induces higher immune response, and may be useful for developing a better vaccine for leptospirosis.
钩端螺旋体病是一种由致病性钩端螺旋体引起的全球性人畜共患病,该属已鉴定出250多种血清型。商业菌苗疫苗存在局限性,即它们既缺乏针对异源血清型的交叉保护,也缺乏长期保护。本研究在小鼠中研究了一种抗钩端螺旋体疫苗的免疫原性,使用外膜蛋白LipL32和Loa22作为抗原。将该疫苗制剂的免疫原性与单独基于LipL32或Loa22的疫苗所诱导的免疫原性进行了比较。使用DNA包裹的壳聚糖纳米颗粒进行体内DNA递送。使用表达lipL32和loa22的独特DNA质粒进行疫苗接种,比分别组合携带每个基因的质粒时诱导出更高的抗体反应。因此,该制剂用于测试通过异源初免(DNA)-加强(蛋白质)免疫方案给药时的免疫原性。联合接受两种抗原的小鼠中针对LipL32(总IgG和IgG1)和Loa22(IgG1)的特异性抗体反应高于单独接种单一抗原的小鼠。尽管在所有接种疫苗的小鼠组中未观察到脾CD4+T细胞增殖的显著差异,但在体外再刺激时,接种两种抗原的小鼠的脾细胞产生的干扰素-γ和IL-2比单独使用单一抗原时更高。综上所述,使用壳聚糖作为DNA递送系统的异源初免-加强免疫方案中,LipL32和Loa22抗原诱导的免疫原性可诱导更高的免疫反应,可能有助于开发更好的钩端螺旋体病疫苗。