Melchers I, Fey K, Eichmann K
J Exp Med. 1982 Dec 1;156(6):1587-603. doi: 10.1084/jem.156.6.1587.
Splenic T cells exposed to concanavalin A (Con A), and subsequently to factors produced by rat spleen cells in response to Con A (Con A sup), acquire the ability to function as helper T (TH) cells in response to xenogeneic erythrocytes (RBC). Help is measured as the reconstitution of the plaque-forming cell response of a spleen cell population depleted of T cells by treatment with anti-Thy-1 serum and complement. We propose that precursor TH cells differentiate during the in vitro treatment into mature TH cells. As differentiation occurs under limiting dilution conditions, an estimation of the precursor frequency should in principle be possible. However, a single-hit Poisson distribution does not fit our data. Instead, we observe, dependent on the T cell concentration, three separate "peaks" of response. In many experiments, using sheep, horse, and chicken RBC as antigens, we reproducibly find these "peaks" at 40-190, 600-3,000, and 20,000-100,000 T cells, placed into limiting dilution cultures, respectively. By various experiments we can show that the helper activity is not due to passively transferred rat factors, but to the titrated cells themselves. The active cell is a T cell that appears to function in an antigen-specific way and to require direct cell contact to do so. It thus resembles the classical helper T cell. As we find precursor TH cells already at very low concentrations of T cells, we titrated the range between 0 and 100 T cells/well carefully. The bent shape of the titration curves does not always allow a statistically satisfying regression analysis, and we therefore cannot estimate precise precursor frequencies from every experiment. However, a common sense argument can be made that these frequencies must be on the order of 1/10-1/100 T cells. We propose that the limiting dilution curves obtained in this system most likely reflect fundamentally important cellular interactions that regulate immunological effector functions. We favor a concept of independently interacting sets of helper and suppressor T cells of various frequencies, but other models are possible.
暴露于伴刀豆球蛋白A(Con A)的脾T细胞,随后再接触大鼠脾细胞针对Con A产生的因子(Con A sup),获得了针对异种红细胞(RBC)发挥辅助性T(TH)细胞功能的能力。辅助作用通过用抗Thy-1血清和补体处理使T细胞耗竭的脾细胞群体的空斑形成细胞反应的重建来衡量。我们提出前体TH细胞在体外处理过程中分化为成熟的TH细胞。由于分化是在有限稀释条件下发生的,原则上应该可以估计前体频率。然而,单打击泊松分布并不适合我们的数据。相反,我们观察到,根据T细胞浓度的不同,有三个独立的反应“峰值”。在许多实验中,使用绵羊、马和鸡的RBC作为抗原,我们在分别放入有限稀释培养物的40 - 190、600 - 3000和20000 - 100000个T细胞时,可重复性地发现这些“峰值”。通过各种实验我们可以表明,辅助活性不是由于被动转移的大鼠因子,而是由于滴定的细胞本身。活性细胞是一种T细胞,似乎以抗原特异性方式发挥作用,并且需要直接的细胞接触才能如此。因此它类似于经典的辅助性T细胞。由于我们在非常低的T细胞浓度下就已经发现了前体TH细胞,我们仔细滴定了每孔0到100个T细胞的范围。滴定曲线的弯曲形状并不总是允许进行统计学上令人满意的回归分析,因此我们无法从每个实验中估计精确的前体频率。然而,可以有一个合理的观点认为这些频率必须在1/10 - 1/100个T细胞的数量级上。我们提出在该系统中获得的有限稀释曲线很可能反映了调节免疫效应功能的根本重要的细胞相互作用。我们倾向于一种不同频率的辅助性和抑制性T细胞独立相互作用组的概念,但其他模型也是可能的。