Interleukin 2 (IL2) was discovered by Morgan et al. in 1976. Since then its unique functional property which induces the in vitro growth of antigen-stimulated T cells, especially cytotoxic T cells (CTL) opened a way to establish the T cell clone and gave us a way to explore the nature of T cell receptor molecule. Several kinds of T lymphoma cell lines or T hybridomas of mouse or human origin which produce IL2 have been established and the biochemical and functional properties of IL2 have been extensively studied. One of the important findings in Immunology is the discovery that IL2 exerts its function through the receptor on the antigen-activated T cells as peptide hormone does. The antigen-specific response of immunocompetent cells is assured by the antigen-specific appearance of IL2 receptor and by the fact that only the cells which have acquired the receptor can respond to IL2 to proliferate and differentiate to effector cells. Thus antigen-non-specific T cell factor such as IL2 can successfully function in the antigen-specific manner. Human IL2 cDNA has been cloned by the monumental achievement of Taniguchi et al. They determined the complete nucleotide sequence of IL2 cDNA and succeeded in the expression of IL2 cDNA in monkeys cell line, COS-7 cells. Their work gave us a chance to use pure IL2 which was produced by a cloned cDNA and thus a lot of reported studies on the functional properties of IL2 which have been done by using IL2 preparation contaminating a lot of other factors will be reevaluated and the true functions of IL2 will be established in near future. Up to present day, the in vivo effects of IL2 have not yet been established. Some encouraging studies showed the in vivo effects of IL2 and the successful therapeutic effects against tumor by co-administration of IL2 with tumor-specific CTL. It is now possible to use the product of a cloned IL2 cDNA to investigate the in vivo effects of IL2. It is highly expected that the promising results will be obtained and the application of several kinds of lymphokines such as IL2 to clinical fields will become possible.
白细胞介素2(IL2)于1976年由摩根等人发现。自那时起,其诱导抗原刺激的T细胞(尤其是细胞毒性T细胞,CTL)体外生长的独特功能特性,为建立T细胞克隆开辟了道路,并为我们探索T细胞受体分子的本质提供了途径。已经建立了几种产生IL2的小鼠或人源T淋巴瘤细胞系或T杂交瘤,并对IL2的生化和功能特性进行了广泛研究。免疫学的重要发现之一是,IL2像肽激素一样通过抗原激活的T细胞上的受体发挥作用。免疫活性细胞的抗原特异性反应通过IL2受体的抗原特异性出现以及只有获得该受体的细胞才能对IL2作出反应以增殖并分化为效应细胞这一事实来保证。因此,诸如IL2之类的抗原非特异性T细胞因子能够以抗原特异性方式成功发挥作用。人类IL2 cDNA已由谷口等人的巨大成就克隆出来。他们确定了IL2 cDNA的完整核苷酸序列,并成功地在猴细胞系COS-7细胞中表达了IL2 cDNA。他们的工作使我们有机会使用由克隆的cDNA产生的纯IL2,因此,许多使用污染了许多其他因子的IL2制剂进行的关于IL2功能特性的报道研究将被重新评估,并且IL2的真正功能将在不久的将来得以确立。到目前为止,IL2的体内作用尚未明确。一些令人鼓舞的研究显示了IL2的体内作用以及通过将IL2与肿瘤特异性CTL共同给药对肿瘤的成功治疗效果。现在可以使用克隆的IL2 cDNA产物来研究IL2的体内作用。人们高度期望能获得有前景的结果,并且诸如IL2之类的几种淋巴因子在临床领域的应用将成为可能。