Pollock Kevin G J, Conacher Margaret, Wei Xiao-Qing, Alexander James, Brewer James M
Department of Immunology and Bacteriology, University of Glasgow, Western Infirmary, Glasgow, UK.
Immunology. 2003 Feb;108(2):137-43. doi: 10.1046/j.1365-2567.2003.01581.x.
Previous studies have shown that the antigen-specific T helper 2 (Th2) response induced by alum adjuvants is interleukin (IL)-4 independent. As a role for IL-18 in Th2 induction has recently been described, in addition to its role in enhancing Th1 responses, we have studied the Th2 response induced by ovalbumin (OVA) adsorbed to alum in wild-type and IL-18-deficient mice. Our results indicate that while endogenous IL-18 facilitates alum-induced IL-4 production, OVA-specific immunoglobulin G1 (IgG1) and IgE production remain unaffected. Furthermore, antigen-specific Th1 responses induced with alum/IL-12-adsorbed OVA were demonstrated to be highly IL-18 dependent. Despite these observations, injection of BALB/c mice with exogenous IL-18 adsorbed to alum/OVA did not alter IL-4 or interferon-gamma production by T cells and had little effect on the relative production of IgG1/IgG2a antibody subclasses compared with alum/OVA inoculated mice. However, the previously described synergism between IL-12 and IL-18 in Th1 induction was evident as the Th1-promoting activity of alum/IL-12 against adsorbed OVA was greatly augmented by the coadministration of IL-18. These results indicate that while alum-induced IL-18 can facilitate Th2 induction, the addition of exogenous IL-18 cannot further enhance the alum-induced Th2 response.
先前的研究表明,明矾佐剂诱导的抗原特异性辅助性T细胞2(Th2)反应不依赖白细胞介素(IL)-4。由于最近已描述了IL-18在Th2诱导中的作用,除了其在增强Th1反应中的作用外,我们研究了野生型和IL-18缺陷型小鼠中吸附于明矾的卵清蛋白(OVA)诱导的Th2反应。我们的结果表明,虽然内源性IL-18促进明矾诱导的IL-4产生,但OVA特异性免疫球蛋白G1(IgG1)和IgE产生不受影响。此外,已证明用明矾/IL-12吸附的OVA诱导的抗原特异性Th1反应高度依赖IL-18。尽管有这些观察结果,但与接种明矾/OVA的小鼠相比,给BALB/c小鼠注射吸附于明矾/OVA的外源性IL-18并未改变T细胞产生的IL-4或干扰素-γ,并且对IgG1/IgG2a抗体亚类的相对产生影响很小。然而,如IL-18的共同给药极大地增强了明矾/IL-12对吸附OVA的Th1促进活性,因此IL-12和IL-18在Th1诱导中先前描述的协同作用是明显的。这些结果表明,虽然明矾诱导的IL-18可促进Th2诱导,但添加外源性IL-18不能进一步增强明矾诱导的Th2反应。