Jonuleit H, Kühn U, Müller G, Steinbrink K, Paragnik L, Schmitt E, Knop J, Enk A H
Department of Dermatology, University of Mainz, Germany.
Eur J Immunol. 1997 Dec;27(12):3135-42. doi: 10.1002/eji.1830271209.
Culture conditions for human dendritic cells (DC) have been developed by several laboratories. Most of these culture methods, however, have used conditions involving fetal calf serum (FCS) to generate DC in the presence of granulocyte-macrophage colony-stimulating factor and interleukin (IL)-4. Recently, alternative culture conditions have been described using an additional stimulation with monocyte-conditioned medium (MCM) and FCS-free media to generate DC. As MCM is a rather undefined cocktail, the yield and quality of DC generated by these cultures varies substantially. We report that a defined cocktail of tumor necrosis factor (TNF)-alpha, IL-1beta and IL-6 equals MCM in its potency to generate DC. Addition of prostaglandin (PG)E2 to the cytokine cocktail further enhanced the yield, maturation, migratory and immunostimulatory capacity of the DC generated. More importantly, culture conditions also influenced the outcome of the T cell response induced. DC cultured with TNF-alpha/IL-1/IL-6 or MCM alone induced CD4+ T cells that release intermediate levels of interferon (IFN)-gamma and no IL-4 or IL-10. Production of IFN-gamma was significantly induced by addition of PGE2, while no effect on production of IL-4 or IL-10 was observed. Even more striking differences were observed for CD8+ T cells. While MCM conditions only induced IFN-gamma(low), IL-4(neg) cells, TNF-alpha/IL-1/IL-6 promoted growth of IFN-gamma(intermediate), IL-4(neg) CD8+ T cells. Addition of PGE2 again only further polarized this pattern enhancing IFN-gamma production by alloreactive CD8+ T cells in both cultures without inducing type 2 cytokines. Taken together, the data indicate that the defined cocktail TNF-alpha/IL-1/IL-6 can substitute for MCM and that addition of PGE2 further enhances the yield and quality of DC generated. TNF-alpha/IL-1, IL-6 + PGE2-cultured DC seem to be optimal for generation of IFN-gamma-producing CD4/CD8+ T cells.
多个实验室已开发出人类树突状细胞(DC)的培养条件。然而,这些培养方法大多采用含胎牛血清(FCS)的条件,在粒细胞 - 巨噬细胞集落刺激因子和白细胞介素(IL)-4存在的情况下生成DC。最近,有人描述了使用单核细胞条件培养基(MCM)和无FCS培养基进行额外刺激来生成DC的替代培养条件。由于MCM是一种成分相当不明确的混合物,这些培养方法所生成DC的产量和质量差异很大。我们报告,肿瘤坏死因子(TNF)-α、IL-1β和IL-6的特定组合在生成DC的效力上等同于MCM。向细胞因子组合中添加前列腺素(PG)E2进一步提高了所生成DC的产量、成熟度、迁移和免疫刺激能力。更重要的是,培养条件也影响了所诱导的T细胞反应的结果。单独用TNF-α/IL-1/IL-6或MCM培养的DC诱导产生释放中等水平干扰素(IFN)-γ且不产生IL-4或IL-10的CD4 + T细胞。添加PGE2可显著诱导IFN-γ的产生,而未观察到对IL-4或IL-10产生的影响。在CD8 + T细胞中观察到更显著的差异。虽然MCM条件仅诱导产生IFN-γ(低水平)、IL-4(阴性)细胞,但TNF-α/IL-1/IL-6促进了IFN-γ(中等水平)、IL-4(阴性)CD8 + T细胞的生长。添加PGE2再次仅进一步使这种模式极化,增强了两种培养物中同种异体反应性CD8 + T细胞的IFN-γ产生,而不诱导2型细胞因子。综上所述,数据表明特定组合TNF-α/IL-1/IL-6可替代MCM,并且添加PGE2进一步提高了所生成DC的产量和质量。TNF-α/IL-1、IL-6 + PGE2培养的DC似乎最适合生成产生IFN-γ的CD4/CD8 + T细胞。