Vie H, Miller R A
J Immunol. 1986 May 1;136(9):3292-7.
We present here a culture method for the estimation, in human blood, of the number of lymphocytes that can respond to mitogen by producing interleukin 2 (IL 2). T cells are cultured at limiting dilutions with PHA or Con A in the presence of Epstein Barr virus-transformed human lymphoblastoid cells (EB-LCL), and supernatants are tested 3 days later for IL 2 content by a cell proliferation assay. The distribution of negative wells follows the expected Poisson "single-hit" relationship, suggesting that the assay is sensitive to single cells of a single limiting cell type. On average, 16.3% of peripheral blood mononuclear cells can produce IL 2 in such clonal cultures (mean of 12 determinations; SD = 5.6%). Surprisingly, irradiation (up to 2000 rad) of the titrated responder cell population diminishes the estimated frequencies by less than 50%. The ability to detect IL 2 levels in cultures containing only a single, nonproliferating T lymphocyte allows us to estimate the amount of IL 2 generated by an individual effector cell during a 3-day culture interval after mitogen stimulation. The average responding, irradiated T cell generates 0.92 pg of IL 2 (median) within 3 days. The method presented provides a straightforward way to provide independent estimates of responding cell number and of lymphokine production per cell in a variety of clinical situations.
我们在此介绍一种用于估算人血中能够通过产生白细胞介素2(IL-2)对有丝分裂原作出反应的淋巴细胞数量的培养方法。将T细胞以有限稀释度与PHA或Con A一起在爱泼斯坦-巴尔病毒转化的人淋巴母细胞系(EB-LCL)存在的情况下进行培养,3天后通过细胞增殖试验检测上清液中的IL-2含量。阴性孔的分布遵循预期的泊松“单打击”关系,这表明该试验对单一限制细胞类型的单个细胞敏感。平均而言,16.3%的外周血单个核细胞能够在这种克隆培养中产生IL-2(12次测定的平均值;标准差=5.6%)。令人惊讶的是,对滴定的反应细胞群体进行照射(高达2000拉德)使估计频率降低不到50%。在仅含有单个不增殖T淋巴细胞的培养物中检测IL-2水平的能力使我们能够估算有丝分裂原刺激后3天培养间隔内单个效应细胞产生的IL-2量。平均有反应的受照射T细胞在3天内产生0.92皮克IL-2(中位数)。所介绍的方法提供了一种直接的方式,可在各种临床情况下独立估算反应细胞数量和每个细胞的淋巴因子产生量。