Flesch I E, Wandersee A, Kaufmann S H
Department of Immunology, University of Ulm, Germany.
J Immunol. 1997 Jul 1;159(1):7-10.
IL-4 is a major promotor of Th2 differentiation and an antagonist of IFN-gamma production. Although experimental listeriosis is characterized by a Th1 response, IL-4-producing cells were detected in spleens of mice promptly after Listeria monocytogenes infection. We identified this early IL-4 as inducer of the chemokine, monocyte chemoattractant protein-1 (MCP-1), which mainly attracts monocytes/macrophages, but not neutrophils. MCP-1-secreting cells were demonstrable in spleens of mice infected with L. monocytogenes, and IL-4 neutralization with anti-IL-4 mAb 11B11 markedly diminished frequencies of MCP-1-producing cells. Cell depletion experiments and studies with gene disruption mutant mice lacking distinct T cell subsets and surface MHC molecules point to CD4+ NK1+ T cells as a cellular source of early IL-4. Since monocyte infiltration to infective foci contributes to early control of listeriosis, our results suggest that IL-4-producing CD4+ NK1+ T cells participate in the innate immune response against L. monocytogenes through MCP-1 induction.
白细胞介素-4(IL-4)是Th2分化的主要促进因子,也是γ干扰素产生的拮抗剂。尽管实验性李斯特菌病以Th1反应为特征,但在单核细胞增生李斯特菌感染后,小鼠脾脏中很快就检测到了产生IL-4的细胞。我们确定这种早期的IL-4是趋化因子单核细胞趋化蛋白-1(MCP-1)的诱导剂,MCP-1主要吸引单核细胞/巨噬细胞,而不是中性粒细胞。在感染单核细胞增生李斯特菌的小鼠脾脏中可证实有分泌MCP-1的细胞,用抗IL-4单克隆抗体11B11中和IL-4可显著降低产生MCP-1细胞的频率。细胞清除实验以及对缺乏不同T细胞亚群和表面MHC分子的基因敲除突变小鼠的研究表明,CD4+NK1+T细胞是早期IL-4的细胞来源。由于单核细胞浸润到感染灶有助于早期控制李斯特菌病,我们的结果表明,产生IL-