Division of Allergy and Clinical Immunology, Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Eur J Immunol. 2012 Aug;42(8):2073-86. doi: 10.1002/eji.201142346. Epub 2012 Jul 4.
While the nasal mucosa is a potentially useful site for human immunization, toxin-based nasal adjuvants are generally unsafe and less effective in humans. Safe mucosal adjuvants that activate protective immunity via mucosal administration are highly dependent on barrier antigen sampling by epithelial and DCs. Here, we demonstrate that protein antigens formulated in unique oil-in-water nanoemulsions (NEs) result in distinctive transcellular antigen uptake in ciliated nasal epithelial cells, leading to delivery into nasal associated lymphoid tissue. NE formulation also enhances MHC class II expression in epithelial cells and DC activation/trafficking to regional lymphoid tissues in mice. These materials appear to induce local epithelial cell apoptosis and heterogeneous cytokine production by mucosal epithelial cells and mixed nasal tissues, including G-CSF, GM-CSF, IL-1a, IL-1b, IL-5, IL-6, IL-12, IP-10, KC, MIP-1a, TGF-β, and TSLP. This is the first observation of a nasal adjuvant that activates calreticulin-associated apoptosis of ciliated nasal epithelial cells to generate broad cytokine/chemokine responses in mucosal tissue.
虽然鼻腔黏膜是人体免疫的一个潜在有用部位,但基于毒素的鼻腔佐剂在人体中通常是不安全且效果较差的。通过黏膜给予可激活保护性免疫的安全黏膜佐剂高度依赖于上皮细胞和成纤维细胞状细胞对屏障抗原的采样。在这里,我们证明了在独特的油包水纳米乳液(NE)中配制的蛋白质抗原可导致纤毛状鼻上皮细胞中独特的跨细胞抗原摄取,从而递送至鼻相关淋巴组织。NE 制剂还增强了上皮细胞中的 MHC Ⅱ类表达,并激活/迁移至小鼠的区域性淋巴组织中的 DC。这些材料似乎通过黏膜上皮细胞和混合的鼻组织诱导局部上皮细胞凋亡和异质细胞因子产生,包括 G-CSF、GM-CSF、IL-1a、IL-1b、IL-5、IL-6、IL-12、IP-10、KC、MIP-1a、TGF-β 和 TSLP。这是首次观察到鼻腔佐剂可激活纤毛状鼻上皮细胞中钙网蛋白相关的凋亡,从而在黏膜组织中产生广泛的细胞因子/趋化因子反应。