Vine J B, Geppert T D, Lipsky P E
Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas 75235.
J Immunol. 1988 Oct 15;141(8):2593-600.
Soluble mitogens, such as PHA induce accessory cell (AC)-dependent T cell proliferation. One function of the AC is to create a stimulatory matrix. Therefore, experiments were carried out to determine whether PHA immobilized onto microtiter plates could stimulate T cells in the absence of AC. Peripheral blood T4 cells were cultured under limiting dilution conditions with either soluble or immobilized PHA with or without rIL-1 beta, rIL-2, r-TNF-alpha, an anti-CD28 mAb (9.3), or irradiated EBV-transformed B cells as AC. The frequency of proliferating T4 cells was assessed by examining wells microscopically, and the frequency of T4 cells producing IL-2 was assessed by examining the ability of supernatants to support CTLL-2 proliferation. The percentage of T4 cells growing and producing IL-2 was determined by a maximum likelihood procedure. Immobilized, but not soluble, PHA induced a mean of 20.0 +/- 2.6% of T4 cells to grow in the complete absence of AC in medium supplemented with rIL-2. Whereas rIL-1 beta, rTNF-alpha, and 9.3 were unable to support T4 cell growth in the absence of rIL-2, each enhanced the percentage of T4 cells responding to immobilized PHA in the presence of rIL-2. In contrast, both soluble and immobilized PHA were unable to induce T4 cell IL-2 production in the absence of AC, even when cultures were supplemented with rIL-1 beta or 9.3. In the presence of AC, a small percentage of T4 cells (5.4 to 11.7%) was stimulated to produce detectable amounts of IL-2 by either immobilized or soluble PHA. Moreover, in the presence of AC, a very small population (approximately 1%) of PHA-stimulated T4 cells proliferated without supplemental rIL-2. The data indicate that a matrix of immobilized PHA is sufficient for some T4 cells to be activated to respond to IL-2, whereas others require additional signals provided by rIL-1 beta, rTNF alpha, 9.3, or AC. In contrast, neither soluble nor immobilized PHA is sufficient to induce T cell IL-2 production. This response requires signals provided by intact AC.
可溶性丝裂原,如PHA可诱导辅助细胞(AC)依赖性T细胞增殖。AC的一个功能是形成刺激基质。因此,开展实验以确定固定在微量滴定板上的PHA在无AC的情况下是否能刺激T细胞。外周血T4细胞在有限稀释条件下与可溶性或固定化PHA一起培养,添加或不添加rIL-1β、rIL-2、r-TNF-α、抗CD28单克隆抗体(9.3),或经辐照的EBV转化B细胞作为AC。通过显微镜检查孔来评估增殖T4细胞的频率,通过检测上清液支持CTLL-2增殖的能力来评估产生IL-2的T4细胞的频率。通过最大似然法确定生长并产生IL-2的T4细胞的百分比。在补充有rIL-2的培养基中,固定化而非可溶性PHA在完全无AC的情况下可诱导平均20.0±2.6%的T4细胞生长。虽然在无rIL-2的情况下rIL-1β、rTNF-α和9.3无法支持T4细胞生长,但在有rIL-2的情况下,它们均提高了对固定化PHA作出反应的T4细胞的百分比。相反,即使培养物补充了rIL-1β或9.3,可溶性和固定化PHA在无AC的情况下均无法诱导T4细胞产生IL-2。在有AC的情况下,固定化或可溶性PHA均可刺激一小部分T4细胞(5.4%至11.7%)产生可检测量的IL-2。此外,在有AC的情况下,非常小的一部分(约1%)受PHA刺激的T4细胞在无补充rIL-2的情况下增殖。数据表明,固定化PHA基质足以使一些T4细胞被激活以对IL-2作出反应,而其他细胞则需要rIL-1β、rTNF-α、9.3或AC提供的额外信号。相反,可溶性或固定化PHA均不足以诱导T细胞产生IL-2。这种反应需要完整AC提供的信号。