Kurahashi K, Yamamura M, Nakamura K, Kato K, Katsunuma T
Department of Biochemistry, School of Medicine, Tokai University, Kanagawa, Japan.
Tokai J Exp Clin Med. 1988 Dec;13(6):337-44.
This study was carried out to elucidate the interaction of alpha-1-antichymotrypsin (ACT) with the immune reaction induced by interleukin-2 (IL-2). ACT, isolated from human sera and determined to be a single glycoprotein, was added to human peripheral T-cell cultured with IL-2. It was found that ACT effectively suppressed T-cell activation induced by IL-2, but the suppressive effect of ACT was inversely proportional to the concentration of IL-2. A similar effect was found when T-cells were stimulated with PHA. ACT had a suppressive effect when suboptimal concentrations of PHA were used, however this suppressive effect could not be found at the optimal PHA concentration. These findings suggest that ACT may be a regulatory agent in immune reactivity where low concentrations of IL-2 are present. Even under normal conditions, an individual is surrounded and invaded by numerous foreign elements and it may be that small amounts of IL-2 are constantly produced, which would indefinitely trigger chained immune reactions if there were no regulatory agent like ACT.
本研究旨在阐明α-1-抗糜蛋白酶(ACT)与白细胞介素-2(IL-2)诱导的免疫反应之间的相互作用。从人血清中分离并确定为单一糖蛋白的ACT,被添加到用IL-2培养的人外周血T细胞中。发现ACT能有效抑制IL-2诱导的T细胞活化,但ACT的抑制作用与IL-2的浓度呈反比。当用PHA刺激T细胞时也发现了类似的效果。当使用次优浓度的PHA时,ACT具有抑制作用,然而在最佳PHA浓度下未发现这种抑制作用。这些发现表明,在存在低浓度IL-2的免疫反应性中,ACT可能是一种调节因子。即使在正常情况下,个体也会被大量外来物质包围和侵袭,可能会不断产生少量的IL-2,如果没有像ACT这样的调节因子,这将无限期地引发连锁免疫反应。