Orr Mark T, Orgun Nural N, Wilson Christopher B, Way Sing Sing
Department of Immunology, University of Washington School of Medicine, Seattle, WA 98195, USA.
J Immunol. 2007 Apr 15;178(8):4731-5. doi: 10.4049/jimmunol.178.8.4731.
The vast majority of the world's population is infected with HSV. Although antiviral therapy can reduce the incidence of reactivation and asymptomatic viral shedding, and limit morbidity and mortality from active disease, it cannot cure infection. Therefore, the development of an effective vaccine is an important global health priority. In this study, we demonstrate that recombinant Listeria monocytogenes (Lm) expressing the H-2K(b) glycoprotein B (gB)(498-505) peptide from HSV-1 triggers a robust CD8 T cell response to this Ag resulting in protective immunity to HSV infection. Following challenge with HSV-1, immune-competent mice primed with recombinant Lm-expressing gB(498-505) Ag were protected from HSV-induced paralysis. Protection was associated with dramatic reductions in recoverable virus, and early expansion of HSV-1-specific CD8 T cells in the regional lymph nodes. Thus, recombinant Lm-expressing Ag from HSV represents a promising new class of vaccines against HSV infection.
世界上绝大多数人口都感染了单纯疱疹病毒(HSV)。虽然抗病毒治疗可以降低病毒再激活和无症状病毒脱落的发生率,并限制活动性疾病的发病率和死亡率,但它无法治愈感染。因此,开发一种有效的疫苗是全球重要的卫生优先事项。在本研究中,我们证明,表达来自HSV-1的H-2K(b)糖蛋白B(gB)(498-505)肽的重组单核细胞增生李斯特菌(Lm)引发针对该抗原的强大CD8 T细胞反应,从而产生对HSV感染的保护性免疫。在用HSV-1攻击后,用表达gB(498-505)抗原的重组Lm进行免疫的免疫活性小鼠免受HSV诱导的麻痹。保护作用与可恢复病毒的显著减少以及区域淋巴结中HSV-1特异性CD8 T细胞的早期扩增有关。因此,表达来自HSV抗原的重组Lm代表了一类有前景的抗HSV感染新型疫苗。