Rosenwasser L J, Rosenthal A S
J Immunol. 1978 Jun;120(6):1991-5.
The data in this report describe a T cell proliferation assay with nylon wool column-purified murine lymph node lymphocyte from animals immunized by footpad injection of antigen in CFA. It was found that the in vitro immune response of sensitized T cells to soluble protein antigens was functionally dependent on the presence of adherent cells, more specifically macrophages, at all concentrations of in vitro antigen challenge. The response was due to T cells in that cytotoxic treatment of the immune lymphocyte cells with anti-Thy 1.2 serum and complement effectively eliminated the antigen-specific DNA synthetic responses. The antigen-specific proliferation of murine lymphocytes depleted of adhereent cells could not be reconstituted with either guinea pig macrophages nor murine fibroblasts, indicating the existence of species and cell type specificity. In contrast to previous observations in the guinea pig, soluble products of cultured adherent cells could at least partially replace the function of intact macrophages in the response to antigen.
本报告中的数据描述了一种T细胞增殖试验,该试验使用的是来自经足垫注射CFA中抗原免疫的动物的经尼龙毛柱纯化的小鼠淋巴结淋巴细胞。结果发现,在所有体外抗原刺激浓度下,致敏T细胞对可溶性蛋白抗原的体外免疫反应在功能上依赖于贴壁细胞,更具体地说是巨噬细胞的存在。这种反应是由T细胞引起的,因为用抗Thy 1.2血清和补体对免疫淋巴细胞进行细胞毒性处理可有效消除抗原特异性DNA合成反应。去除贴壁细胞的小鼠淋巴细胞的抗原特异性增殖,既不能用豚鼠巨噬细胞也不能用小鼠成纤维细胞重建,这表明存在物种和细胞类型特异性。与先前在豚鼠中的观察结果相反,培养的贴壁细胞的可溶性产物在对抗抗原的反应中至少可以部分替代完整巨噬细胞的功能。