Aoki I, Tanaka S, Ishii N, Minami M, Klinman D M
Department of Pathology, Yokohama City University School of Medicine, Japan.
Eur J Immunol. 1996 Jun;26(6):1388-93. doi: 10.1002/eji.1830260631.
Short-term stimulation of mouse spleen cells in vitro with interleukin (IL)-3 induces the secretion of the Th2 cytokines IL-4 and IL-6. Non-B/non-T cells were the target of this IL-3 effect. However, during long-term antigen-dependent culture, T cells are the major source of IL-4 and IL-6. The addition of IL-3 to such cultures also led to a significant increase in IL-4 and IL-6 production. This Th2 cytokine secretion was amplified by the addition of irradiated non-B/non-T cells at the initiation of culture, and was inhibited by anti-IL-4 antibodies. These findings suggest that IL-3 induces the rapid release of IL-4 and IL-6 by non-B/non-T cells, thereby creating an immune milieu conducive to the development of antigen-specific IL-4 and IL-6-secreting Th2 cells.
在体外,用白细胞介素(IL)-3短期刺激小鼠脾细胞可诱导Th2细胞因子IL-4和IL-6的分泌。非B/非T细胞是这种IL-3效应的靶细胞。然而,在长期抗原依赖性培养过程中,T细胞是IL-4和IL-6的主要来源。向此类培养物中添加IL-3也导致IL-4和IL-6产量显著增加。在培养开始时添加经辐照的非B/非T细胞可放大这种Th2细胞因子的分泌,而抗IL-4抗体则可抑制该分泌。这些发现表明,IL-3诱导非B/非T细胞快速释放IL-4和IL-6,从而营造出有利于抗原特异性分泌IL-4和IL-6的Th2细胞发育的免疫环境。