Auböck J, Niederwieser D, Romani N, Fritsch P, Huber C
Arch Dermatol Res. 1985;277(4):270-5. doi: 10.1007/BF00509079.
Primary human epidermal cell cultures composed of keratinocytes and melanocytes were exposed to supernatants of phytohaemagglutinin (PHA)-stimulated T cells, various lymphokines and interferon-beta, and checked for the emergence of HLA-DR antigen using immunofluorescence and immunoelectron microscopy. HLA-DR expression was induced by the supernatants and human recombinant interferon-gamma (rIFN-gamma), whereas recombinant interferon-alpha 2, interleukin-2 and non-recombinant human interferon-beta had no such effect. The threshold concentration of rIFN-gamma required to induce this phenomenon was 10 IU/ml; no further increase of reaction intensity was observed using doses of more than 100 IU/ml. Maximum reaction intensity was achieved after 72 h of incubation; a minimum of 3 h of incubation with rIFN-gamma followed by 72 h incubation in rIFN-gamma-free medium proved sufficient to induce HLA-DR expression. The inductive effect of the supernatants and rIFN-gamma could be completely abrogated by pretreatment with excess doses of the monoclonal antibody GZ4 specific for human IFN-gamma. Keratinocytes and melanocytes reacted in an identical fashion both qualitatively and quantitatively in all experiments. These data indicate that IFN-gamma possesses specific signal functions in the induction of HLA-DR expression on epidermal cells.
将由角质形成细胞和黑素细胞组成的原代人表皮细胞培养物暴露于植物血凝素(PHA)刺激的T细胞的上清液、各种淋巴因子和干扰素-β中,并使用免疫荧光和免疫电子显微镜检查HLA-DR抗原的出现情况。上清液和重组人干扰素-γ(rIFN-γ)可诱导HLA-DR表达,而重组干扰素-α2、白细胞介素-2和非重组人干扰素-β则无此作用。诱导该现象所需的rIFN-γ阈值浓度为10 IU/ml;使用超过100 IU/ml的剂量未观察到反应强度进一步增加。孵育72小时后达到最大反应强度;在rIFN-γ中孵育至少3小时,然后在无rIFN-γ的培养基中孵育72小时,已证明足以诱导HLA-DR表达。用过量的针对人IFN-γ的单克隆抗体GZ4预处理可完全消除上清液和rIFN-γ的诱导作用。在所有实验中,角质形成细胞和黑素细胞在定性和定量方面均以相同方式反应。这些数据表明,IFN-γ在诱导表皮细胞上的HLA-DR表达中具有特定的信号功能。