Holter W, Majdic O, Kalthoff F S, Knapp W
Institute of Immunology, VIRCC, University of Vienna, Austria.
Eur J Immunol. 1992 Oct;22(10):2765-7. doi: 10.1002/eji.1830221047.
Interleukin (IL)-4 is a cytokine with a broad range of effects on immune cells, however, little is known regarding the regulation of its production in freshly isolated human peripheral blood mononuclear cells (PBMC). Here we report the production of IL-4 in such cells following stimulation with monoclonal antibodies (mAb) directed against different cell surface antigens. We show that triggering via CD2 is more efficient for IL-4 production than triggering via the CD3 complex. The addition of a CD28 mAb enhances IL-4 production approximately threefold. Cell depletion experiments show that among CD2 plus CD28-stimulated PBMC the production of IL-4 is restricted to the CD8-CD45RA-T cell subpopulation. mAb interfering with the binding of IL-2 to its receptor can inhibit the production of IL-4 in CD2 plus CD28-stimulated PBMC. As IL-2 induces cell proliferation and production of interferon-gamma, but not production of IL-4, it follows that IL-2 is necessary but not sufficient for IL-4 production.
白细胞介素(IL)-4是一种对免疫细胞具有广泛作用的细胞因子,然而,对于其在新鲜分离的人外周血单个核细胞(PBMC)中的产生调控知之甚少。在此我们报告,在用针对不同细胞表面抗原的单克隆抗体(mAb)刺激后,此类细胞中IL-4的产生情况。我们表明,通过CD2触发比通过CD3复合物触发对IL-4产生更有效。添加CD28 mAb可使IL-4产生增加约三倍。细胞去除实验表明,在CD2加CD28刺激的PBMC中,IL-4的产生仅限于CD8-CD45RA-T细胞亚群。干扰IL-2与其受体结合的mAb可抑制CD2加CD28刺激的PBMC中IL-4的产生。由于IL-2诱导细胞增殖和干扰素-γ的产生,但不诱导IL-4的产生,因此IL-2对于IL-4的产生是必要的,但不是充分的。