Liu D C, Grun J L, Maurer P H
Department of Pharmacology, Thomas Jefferson University, Philadelphia, Pennsylvania 19107.
Cell Immunol. 1991 Apr 1;133(2):420-33. doi: 10.1016/0008-8749(91)90115-r.
The random amino acid copolymer (Glu60, Phe40)n (GPhe) was previously shown to augment antigen-dependent proliferation of the murine TH2 cell lines DCL-2 and D10.G4.1. In the present study, the addition of GPhe to (Glu36, Lys24, Ala40)n (GLA)-primed BALB/c primary lymph node (1 degree LN) T cell cultures, the source of DCL-2, resulted in significant suppression of both the proliferative and lymphokine response to GLA. Suppression by GPhe of the 1 degree LN response was subsequently shown to be neither antigen- nor haplotype restricted, and was inhibitable by polyclonal anti-GPhe antibodies. Studies were extended to a GLA-reactive T cell hybridoma clone (DL.4G6.1). where significant suppression by GPhe of GLA-stimulated lymphokine production was observed as measured by markedly decreased HT-2 stimulatory activity of the collected supernatants. Subsequent antibody blocking experiments employing the monoclonal anti-murine IL-4 antibody 11B11 revealed that BALB/c GLA-reactive 1 degree LN T cells and DL.4G6.1 did not produce detectable levels of IL-4 in their culture fluids when stimulated by GLA, which suggested that these cells, unlike DCL-2, were TH1-like in nature. The addition of GPhe to the TH1 clones 5.2 and 5.9 resulted in significant suppression of proliferation to homologous antigen (ovalbumin), in contrast to the augmentation observed with the TH2 cell lines DCL-2 and D10.G4.1. It was concluded from these data, that the addition of GPhe to various T cell cultures lead to unusual suppressive and augmenting activities specific for TH1 and TH2 cells, respectively. Although the mechanism for these dichotomous effects of GPhe is as yet undetermined, several possibilities are considered.
随机氨基酸共聚物(Glu60,Phe40)n(GPhe)先前已被证明可增强小鼠TH2细胞系DCL-2和D10.G4.1的抗原依赖性增殖。在本研究中,将GPhe添加到(Glu36,Lys24,Ala40)n(GLA)引发的BALB/c原代淋巴结(1°LN)T细胞培养物(DCL-2的来源)中,导致对GLA的增殖反应和淋巴因子反应均受到显著抑制。随后发现,GPhe对1°LN反应的抑制既不受抗原限制也不受单倍型限制,并且可被多克隆抗GPhe抗体抑制。研究扩展到一个GLA反应性T细胞杂交瘤克隆(DL.4G6.1)。通过收集的上清液对HT-2刺激活性的显著降低来衡量,观察到GPhe对GLA刺激的淋巴因子产生有显著抑制作用。随后使用单克隆抗小鼠IL-4抗体11B11进行的抗体阻断实验表明,BALB/c GLA反应性1°LN T细胞和DL.4G6.1在受到GLA刺激时,其培养液中未产生可检测水平的IL-4,这表明这些细胞与DCL-2不同,本质上是TH1样细胞。与在TH2细胞系DCL-2和D10.G4.1中观察到的增强作用相反,将GPhe添加到TH1克隆5.2和5.9中导致对同源抗原(卵清蛋白)增殖的显著抑制。从这些数据得出结论,将GPhe添加到各种T细胞培养物中分别导致对TH1和TH2细胞特异的异常抑制和增强活性。尽管GPhe这些二分效应的机制尚未确定,但考虑了几种可能性。