Kjerrulf M, Grdic D, Ekman L, Schön K, Vajdy M, Lycke N Y
Department of Medical Microbiology and Immunology, University of Göteborg, Sweden.
Immunology. 1997 Sep;92(1):60-8. doi: 10.1046/j.1365-2567.1997.00312.x.
Interferon-gamma (IFN-gamma) receptor knock-out (IFN-gamma R -/-) mice were used to analyse the role of IFN-gamma in mucosal immune responses following oral immunization. We found that the IFN-gamma R -/- mice demonstrated 50% reduced spot-forming cell (SFC) responses in the gut lamina propria and spleen after oral immunization with keyhold limpet haemocyanin (KLH) plus cholera toxin (CT) adjuvant. The IFN-gamma R -/- mice exhibited 10-fold reduced total serum KLH-specific antibody levels compared with wild-type mice after oral immunization, while after intravenous immunization, no such difference was seen, suggesting a selective impairment of mucosal immune responses. Moreover, oral immunizations resulted in impaired interleukin-4 (IL-4), IL-10 and IFN-gamma production by spleen T cells from IFN-gamma R -/- mice, indicating that no reciprocal up-regulation of Th2-activities had occurred despite the lack of IFN-gamma R function. No reduction in Th1 or Th2 cytokines was observed following systemic immunizations. Despite potentially strong modulating effects of IFN-gamma on epithelial cell IgA transcytosis and electrolyte barrier functions, CT-immunized IFN-gamma R -/- mice demonstrated unaltered protection against CT in ligated intestinal loops together with normal anti-CT IgA and total IgA levels in gut lavage. Oral feeding with KLH followed by parenteral immunization resulted in strongly suppressed SFC numbers and reduced cell-mediated immunity in both wild-type and IFN-gamma R -/- mice. CT-adjuvant abrogated induction of oral tolerance in both IFN-gamma R -/- and wild-type mice. Collectively, our data argue that the two major response patterns induced by oral administration of protein antigen, i.e. active IgA immunity and oral tolerance, are differently regulated. Thus, IFN-gamma R -/- mice have impaired mucosal immune responses while induction of oral tolerance appears to be unaffected by the lack of IFN-gamma functions.
利用干扰素-γ(IFN-γ)受体敲除(IFN-γ R -/-)小鼠分析IFN-γ在口服免疫后黏膜免疫反应中的作用。我们发现,在用钥孔血蓝蛋白(KLH)加霍乱毒素(CT)佐剂进行口服免疫后,IFN-γ R -/-小鼠肠道固有层和脾脏中的斑点形成细胞(SFC)反应降低了50%。与野生型小鼠相比,口服免疫后IFN-γ R -/-小鼠的血清总KLH特异性抗体水平降低了10倍,而静脉注射免疫后未观察到这种差异,这表明黏膜免疫反应存在选择性损伤。此外,口服免疫导致IFN-γ R -/-小鼠脾脏T细胞产生白细胞介素-4(IL-4)、IL-10和IFN-γ受损,这表明尽管缺乏IFN-γ R功能,但Th2活性并未发生相互上调。全身免疫后未观察到Th1或Th2细胞因子减少。尽管IFN-γ对上皮细胞IgA转胞吞作用和电解质屏障功能可能有很强的调节作用,但用CT免疫的IFN-γ R -/-小鼠在结扎肠袢中对CT的保护作用未改变,肠道灌洗液中的抗CT IgA和总IgA水平正常。用KLH口服喂养后进行胃肠外免疫,导致野生型和IFN-γ R -/-小鼠的SFC数量强烈抑制,细胞介导的免疫降低。CT佐剂消除了IFN-γ R -/-和野生型小鼠口服耐受的诱导。总体而言,我们的数据表明,口服蛋白质抗原诱导的两种主要反应模式,即活性IgA免疫和口服耐受,受到不同的调节。因此,IFN-γ R -/-小鼠的黏膜免疫反应受损,而口服耐受的诱导似乎不受IFN-γ功能缺乏的影响。