Physical and Life Sciences Directorate, Lawrence Livermore National Laboratory, 7000 East Avenue, Livermore, CA 94550, USA.
BMC Microbiol. 2012 May 20;12:79. doi: 10.1186/1471-2180-12-79.
Rapid detection and therapeutic intervention for infectious and emerging diseases is a major scientific goal in biodefense and public health. Toward this end, cytokine profiles in human blood were investigated using a human whole blood ex vivo exposure model, called WEEM.
Samples of whole blood from healthy volunteers were incubated with seven pathogens including Yersinia pseudotuberculosis, Yersinia enterocolitica, Bacillus anthracis, and multiple strains of Yersinia pestis, and multiplexed protein expression profiling was conducted on supernatants of these cultures with an antibody array to detect 30 cytokines simultaneously. Levels of 8 cytokines, IL-1α, IL-1β, IL-6, IL-8, IL-10, IP-10, MCP-1 and TNFα, were significantly up-regulated in plasma after bacterial exposures of 4 hours. Statistical clustering was applied to group the pathogens based on the host response protein expression profiles. The nearest phylogenetic neighbors clustered more closely than the more distant pathogens, and all seven pathogens were clearly differentiated from the unexposed control. In addition, the Y. pestis and Yersinia near neighbors were differentiated from the B. anthracis strains.
Cluster analysis, based on host response cytokine profiles, indicates that distinct patterns of immunomodulatory proteins are induced by the different pathogen exposures and these patterns may enable further development into biomarkers for diagnosing pathogen exposure.
快速检测和治疗传染病和新兴疾病是生物防御和公共卫生领域的主要科学目标。为此,使用称为 WEEM 的人体全血体外暴露模型研究了人血液中的细胞因子谱。
将来自健康志愿者的全血样本与包括假结核耶尔森氏菌、肠侵袭性耶尔森氏菌、炭疽芽孢杆菌和多种鼠疫耶尔森氏菌在内的七种病原体一起孵育,并对这些培养物的上清液进行了多重蛋白质表达谱分析,使用抗体阵列同时检测 30 种细胞因子。在细菌暴露 4 小时后,IL-1α、IL-1β、IL-6、IL-8、IL-10、IP-10、MCP-1 和 TNFα 这 8 种细胞因子的水平在血浆中显著上调。应用统计聚类根据宿主反应蛋白表达谱对病原体进行分组。最近的系统发育邻居比更远的病原体聚类更紧密,所有七种病原体都与未暴露的对照明显区分开来。此外,鼠疫耶尔森氏菌和耶尔森氏菌近邻与炭疽芽孢杆菌菌株区分开来。
基于宿主反应细胞因子谱的聚类分析表明,不同病原体暴露诱导了不同的免疫调节蛋白模式,这些模式可能进一步发展为诊断病原体暴露的生物标志物。