Krakauer Teresa
Department of Immunology, Molecular Translational Sciences Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702-5011, USA.
Toxins (Basel). 2015 Feb 13;7(2):553-9. doi: 10.3390/toxins7020553.
Staphylococcal enterotoxin B (SEB) and related exotoxins are important virulence factors produced by Staphylococcus aureus as they cause human diseases such as food poisoning and toxic shock. These toxins bind directly to cells of the immune system resulting in hyperactivation of both T lymphocytes and monocytes/macrophages. The excessive release of proinflammatory cytokines from these cells mediates the toxic effects of SEB. This study examined the inhibitory activities of an anti-inflammatory drug, sulfasalazine, on SEB-stimulated human peripheral blood mononuclear cells (PBMC). Sulfasalazine dose-dependently inhibited tumor necrosis factor α, interleukin 1 (IL-1) β, IL-2, IL-6, interferon γ (IFNγ), and various chemotactic cytokines from SEB-stimulated human PBMC. Sulfasalazine also potently blocked SEB-induced T cell proliferation and NFκB activation. These results suggest that sulfasalazine might be useful in mitigating the toxic effects of SEB by blocking SEB-induced host inflammatory cascade and signaling pathways.
葡萄球菌肠毒素B(SEB)及相关外毒素是金黄色葡萄球菌产生的重要毒力因子,因为它们会引发食物中毒和中毒性休克等人类疾病。这些毒素直接与免疫系统细胞结合,导致T淋巴细胞和单核细胞/巨噬细胞过度活化。这些细胞中促炎细胞因子的过度释放介导了SEB的毒性作用。本研究检测了一种抗炎药物柳氮磺胺吡啶对SEB刺激的人外周血单核细胞(PBMC)的抑制活性。柳氮磺胺吡啶剂量依赖性地抑制了SEB刺激的人PBMC产生的肿瘤坏死因子α、白细胞介素1(IL-1)β、IL-2、IL-6、干扰素γ(IFNγ)以及各种趋化细胞因子。柳氮磺胺吡啶还能有效阻断SEB诱导的T细胞增殖和NFκB活化。这些结果表明,柳氮磺胺吡啶可能通过阻断SEB诱导的宿主炎症级联反应和信号通路,对减轻SEB的毒性作用有用。