Jansen J H, Fibbe W E, Willemze R, Kluin-Nelemans J C
Laboratory for Experimental Hematology, Leiden University Medical Center, The Netherlands.
Blut. 1990 May;60(5):269-74. doi: 10.1007/BF01736226.
Since its discovery in 1982, numerous biological activities of interleukin-4 (IL-4) have been described. Like other cytokines, IL-4 is highly pleiotropic, both with respect to the number of different target cells that are responsive to it and with respect to the number of different biological responses it elicits. Interleukin-4 was initially described as a costimulant for the proliferation of B lymphocytes stimulated with anti-IgM antibody. Synonyms for this cytokine are B cell growth factor-1 (BCGF-1) and B cell stimulatory factor-1 (BSF-1). After cloning of both the murine and human IL-4, the use of recombinant IL-4 enabled detailed studies of its biological functions. Many cell types, mainly of hematological origin, express receptors for IL-4. Accordingly, effects of IL-4 have been described on B lymphocytes, T lymphocytes, NK cells, mononuclear phagocytes, mast cells, fibroblasts and hematopoietic progenitor cells. Currently, there are three major areas in which IL-4 appears to play an important role: 1) regulation of B cell growth and of antibody isotype expression. In this context, a possible role for IL-4 in allergic reactions is of special interest. 2) Stimulation of T cell growth and the generation of cytotoxic T lymphocytes. In addition to the suppressive effects on the induction of non HLA-restricted cellular cytotoxicity by natural killer- (NK) and lymphokine-activated killer (LAK) cells, this suggests a role for IL-4 in the regulation of cellular immune responses. 3) Regulation of the growth and differentiation of hematopoietic bone marrow stem cells. IL-4 itself does not induce proliferation of hematological progenitor cells but it can modulate the growth-factor dependent proliferation of these cells. In this review the biological functions of IL-4, reported until present, are discussed.
自1982年被发现以来,白细胞介素-4(IL-4)的众多生物学活性已被描述。与其他细胞因子一样,IL-4具有高度的多效性,这体现在对其产生反应的不同靶细胞数量以及它引发的不同生物学反应数量方面。白细胞介素-4最初被描述为抗IgM抗体刺激的B淋巴细胞增殖的共刺激因子。这种细胞因子的同义词是B细胞生长因子-1(BCGF-1)和B细胞刺激因子-1(BSF-1)。在克隆了小鼠和人IL-4之后,重组IL-4的使用使得对其生物学功能进行详细研究成为可能。许多主要源自血液系统的细胞类型表达IL-4受体。因此,已经描述了IL-4对B淋巴细胞、T淋巴细胞、NK细胞、单核吞噬细胞、肥大细胞、成纤维细胞和造血祖细胞的作用。目前,IL-4似乎在三个主要领域发挥重要作用:1)B细胞生长和抗体同种型表达的调节。在这种情况下,IL-4在过敏反应中的可能作用特别令人感兴趣。2)T细胞生长的刺激和细胞毒性T淋巴细胞的产生。除了对自然杀伤(NK)细胞和淋巴因子激活的杀伤(LAK)细胞诱导的非HLA限制的细胞毒性的抑制作用外,这表明IL-4在细胞免疫反应调节中起作用。3)造血骨髓干细胞生长和分化的调节。IL-4本身不会诱导血液祖细胞的增殖,但它可以调节这些细胞的生长因子依赖性增殖。在这篇综述中,讨论了迄今为止报道的IL-4的生物学功能。