Yamamoto H, Hirayama M, Genyea C, Kaplan J
Department of Pediatrics, Wayne State University School of Medicine, Children's Hospital of Michigan, Detroit 48201.
J Immunol. 1994 Apr 15;152(8):3842-7.
In addition to generating cells with non-MHC-restricted cytotoxic activity that is characteristic of lymphokine-activated killer (LAK) cells, in vitro cultures of lymphocytes with relatively high concentrations of IL-2 generate cells that simultaneously exhibit two distinct types of suppressor activities: veto, the ability of cells to specifically suppress generation of allo-CTL against their own histocompatibility Ags; and natural suppression, the ability of these same cells to nonspecifically suppress the generation of allo-CTL against both their own and unrelated cell surface Ags. In contrast to veto, which is known to require cell-cell contact between veto-active cells and precursors of CTL, natural suppression is known to be mediated by soluble factors. To identify and characterize suppressor factors that might mediate the natural suppressor activity of IL-2-activated lymphocytes, murine spleen cells were cultured with 1000 U/ml IL-2, and, after varying periods of incubation, their LAK cytolytic activity and natural suppressor activity was determined and cell supernatants were collected and tested for their effects on mixed lymphocyte culture-induced generation of allo-CTL. Like the IL-2-activated lymphocytes themselves, supernatants of these cells nonspecifically inhibited mixed lymphocyte culture-induced generation of allo-CTL. Rabbit anti-TGF-beta specifically neutralized the suppressive effects of both LAK cell supernatants and the IL-2-activated lymphocytes themselves. These findings indicate that TGF-beta is the primary mediator of the natural suppressor activity of IL-2-activated lymphocytes.
除了产生具有非主要组织相容性复合体(MHC)限制的细胞毒性活性的细胞(这是淋巴因子激活的杀伤细胞[LAK细胞]的特征)外,用相对高浓度的白细胞介素-2(IL-2)进行淋巴细胞的体外培养可产生同时表现出两种不同类型抑制活性的细胞:否决,即细胞特异性抑制针对自身组织相容性抗原的同种异体细胞毒性T淋巴细胞(allo-CTL)产生的能力;以及天然抑制,即这些相同细胞非特异性抑制针对自身和无关细胞表面抗原的allo-CTL产生的能力。与已知需要否决活性细胞与CTL前体之间进行细胞接触的否决不同,天然抑制已知是由可溶性因子介导的。为了鉴定和表征可能介导IL-2激活的淋巴细胞天然抑制活性的抑制因子,将小鼠脾细胞与1000 U/ml的IL-2一起培养,并在不同的孵育时间后,测定其LAK细胞溶解活性和天然抑制活性,并收集细胞上清液并测试其对混合淋巴细胞培养诱导的allo-CTL产生的影响。与IL-2激活的淋巴细胞本身一样,这些细胞的上清液非特异性抑制混合淋巴细胞培养诱导的allo-CTL产生。兔抗转化生长因子-β(TGF-β)特异性中和了LAK细胞上清液和IL-2激活的淋巴细胞本身的抑制作用。这些发现表明TGF-β是IL-2激活的淋巴细胞天然抑制活性的主要介质。