Taborski U, Freitag W, Heremans H, Knop J
Immunobiology. 1986 Jul;171(4-5):329-38. doi: 10.1016/s0171-2985(86)80065-1.
The effects of a partially purified, splenocyte-derived murine interferon (MuIFN-gamma N) and a recombinant IFN-gamma (MuIFN-gamma R) on the T suppressor pathway and on the T effector cells of delayed type hypersensitivity were investigated in a 2,4-dinitrofluorobenzene contact sensitivity model. Various T cell subpopulations, suppressor T cells of afferent and efferent types, and an auxiliary T suppressor cells as well as a T effector cell of delayed type hypersensitivity were induced and the functions assessed in transfer experiments. Confirming the results of earlier experiments obtained with IFN-alpha, beta, the MuIFN-gamma N preparation and the rec. MuIFN-gamma R: enhanced the decreased response in animals sensitized with an antigen overload to an optimal response; inhibited the afferent-acting T suppressor cell in vivo and in vitro; inhibited the Ts-eff response; blocked the auxiliary T suppressor cell response after intravenous injection to recipients of Ts-eff cells on day 0 and 1; and did not suppress the activity of the T effector cell of delayed type hypersensitivity in vivo and in vitro (the MuIFN-gamma R was not tested). We conclude that IFN-gamma preferentially inhibited the T suppressor cell circuit of contact allergy. These results are similar to our observations on the inhibitory effects of a pure interferon-alpha, beta on the regulatory T suppressor cell circuit in contact allergy. Selective suppression of different T subpopulations by IFN-gamma may be an important regulatory mechanism in delayed type hypersensitivity.
在2,4-二硝基氟苯接触敏感性模型中,研究了部分纯化的、脾细胞衍生的鼠干扰素(MuIFN-γN)和重组IFN-γ(MuIFN-γR)对迟发型超敏反应的T抑制途径和T效应细胞的影响。诱导了各种T细胞亚群、传入和传出型抑制性T细胞、辅助性T抑制细胞以及迟发型超敏反应的T效应细胞,并在转移实验中评估了它们的功能。与早期使用IFN-α、β、MuIFN-γN制剂和重组MuIFN-γR获得的实验结果一致:增强了因抗原过载致敏的动物中降低的反应至最佳反应;在体内和体外抑制传入作用的T抑制细胞;抑制Ts-eff反应;在第0天和第1天静脉注射给Ts-eff细胞受体后,阻断辅助性T抑制细胞反应;并且在体内和体外不抑制迟发型超敏反应的T效应细胞的活性(未测试MuIFN-γR)。我们得出结论,IFN-γ优先抑制接触性过敏的T抑制细胞回路。这些结果与我们关于纯干扰素-α、β对接触性过敏中调节性T抑制细胞回路的抑制作用的观察结果相似。IFN-γ对不同T亚群的选择性抑制可能是迟发型超敏反应中的一种重要调节机制。