Holán V, Minowada J
Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, Prague.
Immunol Cell Biol. 1993 Dec;71 ( Pt 6):509-15. doi: 10.1038/icb.1993.56.
The relationship between interleukin-1 (IL-1) and interleukin-2 (IL-2) production and immunophenotype marker profiles was studied in a panel of 29 leukaemia and human T cell lymphotropic virus-1 (HTLV-1)-transformed T cell lines. Culture supernatants from six of the 29 T cell lines tested increased IL-2 production by the MOLT-16 cell line in a manner similar to that of rIL-1 alpha or rIL-1 beta. The enhancing activity in the cell culture supernatants was inhibited by antibody against IL-1 alpha. Anti-IL-1 beta antibody had no inhibitory effect. All the cell lines producing IL-1 alpha had characteristics of activated mature T cells. They were terminal deoxyribonucleotidyl transferase (TdT)-, CD4+, CD8-, HLA-DR+ and all were strongly positive for IL-2R alpha (Tac antigen) expression. However, none of the IL-1 alpha producing cell lines secreted detectable IL-2. A significant quantity of IL-2 was found, after stimulation with phytohaemagglutinin, in supernatants from nine of the 29 cell lines tested. The majority of IL-2 producing cell lines originated from less mature, non-activated T cells, as they were characterized by the expression of TdT, lack of HLA-DR antigens and > 50% had no detectable IL-2R alpha. The results thus show that separate, phenotypically different leukaemia and HTLV-1-transformed T cell clones produce IL-1 alpha and IL-2.(ABSTRACT TRUNCATED AT 250 WORDS)
在一组29种白血病和人T细胞白血病病毒1型(HTLV-1)转化的T细胞系中,研究了白细胞介素-1(IL-1)和白细胞介素-2(IL-2)产生与免疫表型标志物谱之间的关系。在所检测的29种T细胞系中,有6种的培养上清液能以类似于重组IL-1α或重组IL-1β的方式增加MOLT-16细胞系的IL-2产生。细胞培养上清液中的增强活性被抗IL-1α抗体抑制。抗IL-1β抗体无抑制作用。所有产生IL-1α的细胞系都具有活化成熟T细胞的特征。它们末端脱氧核苷酸转移酶(TdT)阴性、CD4阳性、CD8阴性、HLA-DR阳性,并且IL-2Rα(Tac抗原)表达均呈强阳性。然而,没有一个产生IL-1α的细胞系分泌可检测到的IL-2。在用植物血凝素刺激后,在所检测的29种细胞系中有9种的上清液中发现了大量IL-2。大多数产生IL-2的细胞系起源于不太成熟、未活化的T细胞,因为它们的特征是TdT表达、缺乏HLA-DR抗原,并且超过50%没有可检测到的IL-2Rα。因此,结果表明,表型不同的白血病和HTLV-1转化的T细胞克隆分别产生IL-1α和IL-2。(摘要截短于250字)