Toll-Like Receptor Activation by Generalized Modules for Membrane Antigens from Lipid A Mutants of Salmonella enterica Serovars Typhimurium and Enteritidis

O. Rossi, M. Caboni, A. Negrea, F. Necchi, R. Alfini, F. Micoli, A. Saul, C. MacLennan, S. Rondini, C. Gerke
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引用次数: 59

Abstract

ABSTRACT Invasive nontyphoidal Salmonella (iNTS) disease is a neglected disease with high mortality in children and HIV-positive individuals in sub-Saharan Africa, caused primarily by Africa-specific strains of Salmonella enterica serovars Typhimurium and Enteritidis. A vaccine using GMMA (generalized modules for membrane antigens) from S. Typhimurium and S. Enteritidis containing lipid A modifications to reduce potential in vivo reactogenicity is under development. GMMA with penta-acylated lipid A showed the greatest reduction in the level of cytokine release from human peripheral blood monocytes from that for GMMA with wild-type lipid A. Deletion of the lipid A modification genes msbB and pagP was required to achieve pure penta-acylation. Interestingly, ΔmsbB ΔpagP GMMA from S. Enteritidis had a slightly higher stimulatory potential than those from S. Typhimurium, a finding consistent with the higher lipopolysaccharide (LPS) content and Toll-like receptor 2 (TLR2) stimulatory potential of the former. Also, TLR5 ligand flagellin was found in Salmonella GMMA. No relevant contribution to the stimulatory potential of GMMA was detected even when the flagellin protein FliC from S. Typhimurium was added at a concentration as high as 10% of total protein, suggesting that flagellin impurities are not a major factor for GMMA-mediated immune stimulation. Overall, the stimulatory potential of S. Typhimurium and S. Enteritidis ΔmsbB ΔpagP GMMA was close to that of Shigella sonnei GMMA, which are currently in phase I clinical trials.
肠沙门氏菌血清型、鼠伤寒和肠炎脂质A突变体膜抗原的toll样受体激活
侵袭性非伤寒沙门菌(iNTS)是撒哈拉以南非洲地区儿童和hiv阳性个体中一种被忽视的高死亡率疾病,主要由非洲特异性肠炎沙门菌血清型鼠伤寒沙门菌和肠炎沙门菌引起。目前正在开发一种利用鼠伤寒沙门氏菌和肠炎沙门氏菌中含有脂质A修饰的GMMA(膜抗原通用模块)疫苗,以减少潜在的体内反应原性。与野生型脂质A相比,五酰化脂质A的GMMA在人外周血单核细胞中细胞因子释放水平的降低幅度最大。脂质A修饰基因msbB和pagP需要被删除才能实现纯五酰化。有趣的是,肠炎沙门氏菌ΔmsbB ΔpagP GMMA的刺激电位略高于鼠伤寒沙门氏菌,这一发现与前者更高的脂多糖(LPS)含量和toll样受体2 (TLR2)刺激电位一致。此外,在沙门氏菌GMMA中发现了TLR5配体鞭毛蛋白。即使将鼠伤寒沙门氏菌的鞭毛蛋白flc以高达总蛋白的10%的浓度添加,也未检测到对GMMA刺激电位的相关贡献,这表明鞭毛蛋白杂质不是GMMA介导的免疫刺激的主要因素。总的来说,鼠伤寒沙门氏菌和肠炎沙门氏菌ΔmsbB ΔpagP GMMA的刺激潜力接近目前处于I期临床试验的索尼氏志贺氏菌GMMA。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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