Siriraj Center of Research of Excellence in Immunoregulation, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Center for Research and Innovation, Faculty of Medical Technology, Mahidol University, Nakhon Pathom, Thailand.
Microb Pathog. 2019 Jul;132:215-221. doi: 10.1016/j.micpath.2019.05.008. Epub 2019 May 7.
Enterovirus 71 (EV71) and coxsackievirus A16 (CA16) are common causative agents of mild and self-limiting symptoms of childhood hand, foot, and mouth disease (HFMD). However, some EV71-infected HFMD patients can develop severe neurological and/or fatal cardiopulmonary complications. In Thailand, HFMD associated with the EV71 subgenotypes C4a and B5 were reported to be associated with diverse outcomes. However, variations in enterovirus subgenotypes and virulence factors have not been fully elucidated; this study elucidated these variations in peripheral blood mononuclear cells (PBMCs) exposed to different subgenotypes of isolated enteroviruses for 24 and 48 h. Following infection, viral titers were determined by plaque assay. Infected cells and intracellular cytokines were quantified using flow cytometry, and multiplex assay was used to examine cytokine release. All isolated subgenotypes showed replication capability in PBMCs; specifically, the replication titer of EV71 C4a tended to be higher than titers of EV71 B5 and CA16. Additionally, the infectivity of EV71 B5 was higher in monocytes than in lymphocytes. Compared with EV71 B5, EV71 C4a and CA16 had greater ability to induce intra- and extracellular cytokine responses. These findings provide new insights into variations in cellular immune responses to different EV71 subgenotypes isolated from Thai patients, which should be considered for the development of vaccines and therapeutic agents.
肠道病毒 71 型(EV71)和柯萨奇病毒 A16 型(CA16)是引起儿童手足口病(HFMD)轻症和自限性症状的常见病原体。然而,一些感染 EV71 的 HFMD 患者可发展为严重的神经和/或致命性心肺并发症。在泰国,报道与 EV71 亚组 C4a 和 B5 相关的 HFMD 与不同的结局有关。然而,肠道病毒亚组和毒力因子的变异尚未完全阐明;本研究阐明了在分离的肠道病毒不同亚组作用下 24 小时和 48 小时外周血单个核细胞(PBMCs)中的这些变异。感染后,通过噬斑法测定病毒滴度。使用流式细胞术定量感染细胞和细胞内细胞因子,并使用多重分析检测细胞因子释放。所有分离的亚组均显示在 PBMCs 中有复制能力;具体而言,EV71 C4a 的复制滴度趋于高于 EV71 B5 和 CA16 的滴度。此外,EV71 B5 在单核细胞中的感染性高于淋巴细胞。与 EV71 B5 相比,EV71 C4a 和 CA16 具有更强的诱导细胞内和细胞外细胞因子反应的能力。这些发现为不同 EV71 亚组引起的细胞免疫反应变异提供了新的见解,这对于疫苗和治疗药物的开发应加以考虑。