Brinkmann V, Geiger T, Alkan S, Heusser C H
Allergy/Immunology, Pharmaceuticals Research Division, Ciba-Geigy Limited, Basel, Switzerland.
J Exp Med. 1993 Nov 1;178(5):1655-63. doi: 10.1084/jem.178.5.1655.
An increased ratio of T helper type 2 (Th2)- vs Th1-like cells contributes to the immune dysregulation in allergic disease situations and in many chronic infections, including AIDS. Th2-type immune responses are characterized by Th cells that produce increased levels of interleukin-4 (IL-4) and decreased levels of interferon gamma (IFN-gamma). The induction of either a Th1- or a Th2-like phenotype may be critically controlled by the antigen-presenting cells and their cytokines, e.g., IFN-alpha. In this study we have determined the frequencies of potential IL-4- and/or IFN-gamma-producing T cells in the peripheral blood of randomly selected healthy individuals, and analyzed whether IFN-alpha controls IL-4 and/or IFN-gamma production. Purified CD4+ or CD8+ T cells were stimulated for 24 h via the T cell receptor/CD3 complex in the presence or absence of IFN-alpha, and single IL-4- and IFN-gamma-secreting cells were detected in enzyme-linked immunospot assays. In the absence of IFN-alpha, CD4 cells produced IFN-gamma at frequencies of 1:50-300, and produced IL-4 at frequencies of 1:110-<1:100,000. Addition of IFN-alpha during the activation of CD4 cells increased the levels of IFN-gamma mRNA. As a consequence, the numbers of IFN-gamma-producing CD4 cells and the amounts of secreted IFN-gamma increased 10-fold. In contrast, IFN-alpha did not increase the frequency of IL-4-secreting CD4 cells. In the absence of IFN-alpha, addition of exogenous IL-4 to cultures of CD4 cells suppressed IFN-gamma secretion by 70%. However, in the presence of IFN-alpha, IL-4 did not display any suppressive effect. Compared with CD4 cells, CD8 cells produced IFN-gamma more frequently (1:5-10) but IL-4 less frequently (1:5,300 to < 1:100,000). IFN-alpha did not display any effect on the frequency of either IFN-gamma or IL-4 production by CD8 cells. Taken together the results indicate that IFN-alpha increases the frequency of IFN-gamma-secreting CD4 Th cells and antagonizes the suppressive effect of IL-4 on IFN-gamma production. As a consequence, IFN-alpha may favor the induction and maintenance of Th1-like cells and thereby counteract Th2-driven allergic immune responses.
辅助性T细胞2型(Th2)与Th1样细胞的比例增加,会导致过敏性疾病以及包括艾滋病在内的许多慢性感染中的免疫失调。Th2型免疫反应的特征是Th细胞产生的白细胞介素-4(IL-4)水平升高,而干扰素γ(IFN-γ)水平降低。Th1或Th2样表型的诱导可能受到抗原呈递细胞及其细胞因子(如IFN-α)的严格控制。在本研究中,我们测定了随机选择的健康个体外周血中潜在产生IL-4和/或IFN-γ的T细胞频率,并分析了IFN-α是否控制IL-4和/或IFN-γ的产生。在有或没有IFN-α的情况下,通过T细胞受体/CD3复合物刺激纯化的CD4+或CD8+T细胞24小时,并在酶联免疫斑点试验中检测单个分泌IL-4和IFN-γ的细胞。在没有IFN-α的情况下,CD4细胞产生IFN-γ的频率为1:50 - 300,产生IL-4的频率为1:110 - <1:100,000。在激活CD4细胞期间添加IFN-α会增加IFN-γ mRNA的水平。结果,产生IFN-γ的CD4细胞数量和分泌的IFN-γ量增加了10倍。相比之下,IFN-α并没有增加分泌IL-4的CD4细胞的频率。在没有IFN-α的情况下,向CD4细胞培养物中添加外源性IL-4可使IFN-γ分泌减少70%。然而,在有IFN-α的情况下,IL-4没有显示出任何抑制作用。与CD4细胞相比,CD8细胞更频繁地产生IFN-γ(1:5 - 10),但产生IL-4的频率较低(1:5,300至<1:100,000)。IFN-α对CD8细胞产生IFN-γ或IL-4的频率没有任何影响。综合这些结果表明,IFN-α增加了分泌IFN-γ的CD4 Th细胞的频率,并拮抗了IL-4对IFN-γ产生的抑制作用。因此,IFN-α可能有利于Th1样细胞的诱导和维持,从而抵消Th2驱动的过敏性免疫反应。