Dautry-Varsat A, Hémar A, Cornet V, Duprez V
Unité de Génétique Somatique (UA CNRS 361), Institut Pasteur, Paris, France.
Blood. 1988 Aug;72(2):588-92.
The effect of cyclosporin A (CsA), a potent immunosuppressive agent, on a human T-cell line, IARC 301, which constitutively secretes interleukin-2 (IL-2) and expresses high-affinity IL-2 receptors, was investigated. We show that CsA inhibits IARC 301 cell growth. CsA also prevents the constitutive secretion of IL-2 in this T-cell line by blocking transcription of the IL-2 gene. If exogenous IL-2 is added together with CsA for 3 days, the cells grow as well as untreated controls. Thus, under such conditions, CsA inhibits IARC 301 growth by preventing its endogenous constitutive IL-2 synthesis. This demonstrates that IL-2 stimulates the proliferation of this cell line by an autocrine pathway, in agreement with our previous data. We also show for the first time, that CsA not only can inhibit IL-2 production of T cells upon activation, but that it can also prevent ongoing constitutive IL-2 synthesis of a T-cell line. Autocrine growth stimulation of tumor cells by cytokines has been demonstrated in a few cases. CsA inhibits synthesis of several cytokines. Probing for the autocrine growth of tumor cells by studying the effect of CsA and its reversibility by cytokines on their proliferation may be simple and useful.
研究了强效免疫抑制剂环孢素A(CsA)对人T细胞系IARC 301的作用,该细胞系组成性分泌白细胞介素2(IL-2)并表达高亲和力IL-2受体。我们发现CsA抑制IARC 301细胞生长。CsA还通过阻断IL-2基因的转录来阻止该T细胞系中IL-2的组成性分泌。如果将外源性IL-2与CsA一起添加3天,细胞的生长情况与未处理的对照相同。因此,在这种条件下,CsA通过阻止其内源性组成性IL-2合成来抑制IARC 301的生长。这表明IL-2通过自分泌途径刺激该细胞系的增殖,这与我们之前的数据一致。我们还首次表明,CsA不仅可以抑制激活后T细胞的IL-2产生,还可以阻止T细胞系中正在进行的组成性IL-2合成。在少数情况下,已证明细胞因子对肿瘤细胞有自分泌生长刺激作用。通过研究CsA的作用及其被细胞因子逆转对肿瘤细胞增殖的影响来探索肿瘤细胞的自分泌生长可能是简单而有用的。