Scheynius A, Larsson P, Skoglund C, Holmdahl R, Klareskog L
Department of Clinical Immunology, Karolinska Institute, Stockholm, Sweden.
Scand J Immunol. 1989 Jun;29(6):671-7. doi: 10.1111/j.1365-3083.1989.tb01171.x.
An important question in local immune regulation in the skin is how keratinocytes at inflammatory sites can modify a local T-cell response to antigens introduced via the skin. In the present study we investigated the effects of rat epidermal cells obtained from the site of a tuberculin reaction, on the proliferative response of a syngeneic purified protein derivative (PPD)-specific CD4+ T-cell line. Epidermal cell suspensions from the tuberculin-reactive ears contained 23-37% cells expressing class II transplantation antigens as judged by immunocytochemistry compared with 2-3% in normal epidermis. When comparing the capacity of these two different epidermal cell populations to induce a PPD-specific T-cell response in vitro, it was found that the PPD-reactive epidermal cells induced a lower T-cell response than did normal epidermal cells. This discrepancy cannot be explained by an infiltration of inflammatory cells into the epidermis of tuberculin-reactive ears. Our data indicate that epidermal cells modified during a delayed-type hypersensitivity reaction in vivo may suppress an antigen-specific T-cell proliferation.
皮肤局部免疫调节中的一个重要问题是,炎症部位的角质形成细胞如何改变对经皮肤引入抗原的局部T细胞反应。在本研究中,我们调查了从结核菌素反应部位获取的大鼠表皮细胞,对同基因纯化蛋白衍生物(PPD)特异性CD4+ T细胞系增殖反应的影响。通过免疫细胞化学判断,来自结核菌素反应耳部的表皮细胞悬液中,有23%-37%的细胞表达II类移植抗原,而正常表皮中这一比例为2%-3%。当比较这两种不同表皮细胞群体在体外诱导PPD特异性T细胞反应的能力时,发现PPD反应性表皮细胞诱导的T细胞反应低于正常表皮细胞。这种差异不能用炎性细胞浸润到结核菌素反应耳部的表皮来解释。我们的数据表明,体内迟发型超敏反应过程中发生改变的表皮细胞可能会抑制抗原特异性T细胞增殖。