Fahlén-Yrlid Linda, Gustafsson Tobias, Westlund Jessica, Holmberg Anna, Strömbeck Anna, Blomquist Margareta, MacPherson Gordon G, Holmgren Jan, Yrlid Ulf
Department of Microbiology and Immunology, Institute of Biomedicine, The Mucosal Immunobiology and Vaccine Center, University of Gothenburg Vaccine Research Institute, Göteborg, Sweden.
J Immunol. 2009 Oct 15;183(8):5032-41. doi: 10.4049/jimmunol.0803992. Epub 2009 Sep 28.
To generate vaccines that protect mucosal surfaces, a better understanding of the cells required in vivo for activation of the adaptive immune response following mucosal immunization is required. CD11c(high) conventional dendritic cells (cDCs) have been shown to be necessary for activation of naive CD8(+) T cells in vivo, but the role of cDCs in CD4(+) T cell activation is still unclear, especially at mucosal surfaces. The activation of naive Ag-specific CD4(+) T cells and the generation of Abs following mucosal administration of Ag with or without the potent mucosal adjuvant cholera toxin were therefore analyzed in mice depleted of CD11c(high) cDCs. Our results show that cDCs are absolutely required for activation of CD4(+) T cells after oral and nasal immunization. Ag-specific IgG titers in serum, as well as Ag-specific intestinal IgA, were completely abrogated after feeding mice OVA and cholera toxin. However, giving a very high dose of Ag, 30-fold more than required to detect T cell proliferation, to cDC-ablated mice resulted in proliferation of Ag-specific CD4(+) T cells. This proliferation was not inhibited by additional depletion of plasmacytoid DCs or in cDC-depleted mice whose B cells were MHC-II deficient. This study therefore demonstrates that cDCs are required for successful mucosal immunization, unless a very high dose of Ag is administered.
为了研发能保护黏膜表面的疫苗,需要更深入地了解黏膜免疫后在体内激活适应性免疫反应所需的细胞。已证明CD11c(高表达)传统树突状细胞(cDCs)对于体内初始CD8⁺ T细胞的激活是必需的,但cDCs在CD4⁺ T细胞激活中的作用仍不清楚,尤其是在黏膜表面。因此,在缺失CD11c(高表达)cDCs的小鼠中,分析了在有或没有强效黏膜佐剂霍乱毒素的情况下,黏膜给予抗原后初始抗原特异性CD4⁺ T细胞的激活以及抗体的产生。我们的结果表明,口服和鼻内免疫后,cDCs对于CD4⁺ T细胞的激活是绝对必需的。给小鼠喂食卵清蛋白(OVA)和霍乱毒素后,血清中的抗原特异性IgG滴度以及肠道中的抗原特异性IgA完全消失。然而,给cDC缺失的小鼠给予非常高剂量的抗原(比检测T细胞增殖所需剂量高30倍),会导致抗原特异性CD4⁺ T细胞增殖。这种增殖不受浆细胞样DCs的额外缺失的抑制,也不受B细胞MHC-II缺陷的cDC缺失小鼠的抑制。因此,这项研究表明,除非给予非常高剂量的抗原,否则cDCs是成功进行黏膜免疫所必需的。