Süss J, Vogt K H, Stiller K J, Stelzner A, Schmidt J
Acta Biol Med Ger. 1979;38(1):107-18.
A rapid and precise method for the assay of cell-mediated immune response basing on protein synthesis stimulation of mitogen-activated guinea pig lymphocytes is modified in a way that enables the study of virus-immunological problems. When used as a micromethod it has the following advantages over conventional methods: short-term cell culture, need of low quantities of cells and rapid preparation of great numbers of samples for radioactivity measurements. In this study we report the results of comparative experiments on measuring lymphocyte stimulation after addition of PHA and stimulation of sensitized lymphocytes following contact with homologous influenza virus antigen in vitro. The most important reaction parameters are as follows: 5-6 . 10(5) spleen lymphocytes/microculture in microtiter plates, use of Eagles's MEM cell culture medium without leucine, supplemented with HEPES buffer and 10% autologous guinea pig serum; optimum lymphocyte stimulation by addition of 0.5 microliter PHA or 0.1-1.0 microgram virus protein/ml; immuno-stimulation by PHA can be measured in vitro already after 6 h and by influenzavirus antigen already after 24 h.
一种基于丝裂原激活的豚鼠淋巴细胞蛋白质合成刺激来检测细胞介导免疫反应的快速精确方法,经过改进后可用于研究病毒免疫学问题。当作为微量方法使用时,它相对于传统方法具有以下优点:短期细胞培养、所需细胞量少以及能快速制备大量用于放射性测量的样品。在本研究中,我们报告了添加PHA后测量淋巴细胞刺激以及体外接触同源流感病毒抗原后致敏淋巴细胞刺激的对比实验结果。最重要的反应参数如下:在微量滴定板中每微培养物5 - 6×10⁵个脾淋巴细胞,使用不含亮氨酸的伊格尔氏MEM细胞培养基,添加HEPES缓冲液和10%自体豚鼠血清;添加0.5微升PHA或0.1 - 1.0微克病毒蛋白/毫升可实现最佳淋巴细胞刺激;PHA诱导的免疫刺激在6小时后即可在体外检测到,流感病毒抗原诱导的免疫刺激在24小时后即可检测到。