Kita E, Kamikaidou N, Oku D, Nakano A, Katsui N, Kashiba S
Department of Bacteriology, Nara Medical University, Japan.
Nat Immun. 1992 Jan-Feb;11(1):46-55.
The present study was carried out to ascertain whether the active component of Corynebacterium kutscheri (CK-M) could stimulate host cells of mice to produce several cytokines. CK-M stimulated thioglycollate-induced peritoneal macrophages to produce interleukin 1 (IL-1) and tumor necrosis factor alpha (TNF-alpha) at concentrations of 1-100 ng/ml, and it also induced IL-2 and interferon-gamma (IFN-gamma) as well as IL-6 production by splenocytes. Maximum production of each cytokine induced by CK-M was obtained at the following doses: IL-1 at 5 ng/ml, TNF-alpha at 50 ng/ml, IL-2 at 1 microgram/ml, IL-6 at 500 ng/ml and IFN-gamma at 750 ng/ml. In contrast, IL-4 was not produced to a significant extent by CK-M-stimulated splenocytes. Furthermore, when mice were intravenously injected with 20 micrograms of CK-M, IL-2 and IFN-gamma production by splenocytes, upon stimulation with either formalin-killed C. kutscheri or mitogens, was significantly higher on day 10 of treatment than on day 2. Additionally, the cytotoxicity to L929 cells of this serum from CK-M-treated mice increased with time, and the activity in the serum of day 10 was not abrogated by the antibody to TNF-alpha. Data obtained here indicate that CK-M may preferentially stimulate type-1 helper T cells to produce IL-2 and IFN-gamma, and that the enhanced cytokine production could contribute to the nonspecific resistance induced by C. kutscheri.
本研究旨在确定科氏棒状杆菌(CK-M)的活性成分是否能刺激小鼠宿主细胞产生多种细胞因子。CK-M在浓度为1-100 ng/ml时,刺激巯基乙酸诱导的腹腔巨噬细胞产生白细胞介素1(IL-1)和肿瘤坏死因子α(TNF-α),它还诱导脾细胞产生IL-2、干扰素-γ(IFN-γ)以及IL-6。CK-M诱导的每种细胞因子的最大产量在以下剂量时获得:IL-1为5 ng/ml,TNF-α为50 ng/ml,IL-2为1微克/ml,IL-6为500 ng/ml,IFN-γ为750 ng/ml。相比之下,CK-M刺激的脾细胞未大量产生IL-4。此外,当给小鼠静脉注射20微克CK-M时,在第10天,经福尔马林灭活的科氏棒状杆菌或有丝分裂原刺激后,脾细胞产生的IL-2和IFN-γ显著高于第2天。另外,CK-M处理小鼠的血清对L929细胞的细胞毒性随时间增加,且第10天血清中的活性不会被抗TNF-α抗体消除。此处获得的数据表明,CK-M可能优先刺激1型辅助性T细胞产生IL-2和IFN-γ,且细胞因子产生的增强可能有助于科氏棒状杆菌诱导的非特异性抵抗力。