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Glycans from avian influenza virus are recognized by chicken dendritic cells and are targets for the humoral immune response in chicken

机译:禽流感病毒的聚糖被鸡树突状细胞识别,是鸡体液免疫反应的靶标

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To increase our understanding of the interaction between avian influenza virus and its chicken host, we identified receptors for putative avian influenza virus (AIV) glycan determinants on chicken dendritic cells. Chicken dendritic cells (DCs) were found to recognize glycan determinants containing terminal αGalNAc, Galα1-3Gal, GlcNAcβ1-4GlcNAcβ1-4GlcNAcβ (chitotriose) and Galα1-2Gal. Infection of chicken dendritic cells with either low pathogenic (LP) or highly pathogenic (HP) AIV results in elevated mRNA expression of homologs of the mouse C-type lectins DEC205 and macrophage mannose receptor (MMR), whereas expression levels of the human dendritic cell-specific intercellular adhesion molecule-3-grabbing non-integrin (DC-SIGN) homolog remained unchanged.Following uptake and subsequent presentation of avian influenza virus by DCs, adaptive immunity, including humoral immune responses are induced. We have investigated the antibody responses against virus glycan epitopes after avian influenza virus infection. Using glycan micro-array analysis we showed that chicken contained antibodies that predominantly recognize terminal Galα1-3Gal-R, chitotriose and Fucα1-2Galβ1-4GlcNAc-R (H-type 2). After influenza-infection, glycan array analysis showed that both levels and repertoire of glycan-recognizing antibodies decreased. However, analysis of the sera by ELISA indicated that the levels of different isotypes of anti-glycan Abs against specific glycan antigens was increased after influenza-infection, suggesting that the presentation of the glycan antigens and iso-type of the Abs are critical parameters to take into account when measuring anti-glycan Abs. This novel approach in avian influenza research may contribute to the development of a broad spectrum vaccine and improves our mechanistic understanding of innate and adaptive responses to glycans.
机译:为了增加我们对禽流感病毒与其鸡宿主之间相互作用的了解,我们鉴定了鸡树突状细胞上假定的禽流感病毒(AIV)聚糖决定簇的受体。发现鸡树突状细胞(DC)识别包含末端αGalNAc,Galα1-3Gal,GlcNAcβ1-4GlcNAcβ1-4GlcNAcβ(壳三糖)和Galα1-2Gal的聚糖决定簇。用低致病性(LP)或高致病性(HP)AIV感染鸡树突状细胞会导致小鼠C型凝集素DEC205和巨噬细胞甘露糖受体(MMR)同源物的mRNA表达升高,而人树突状细胞的表达水平升高特异性细胞间粘附分子3-捕获非整联蛋白(DC-SIGN)同源物保持不变。在DC吸收并随后呈递禽流感病毒之后,诱导了包括体液免疫反应在内的适应性免疫。我们已经研究了禽流感病毒感染后针对病毒聚糖表位的抗体反应。使用聚糖微阵列分析,我们发现鸡所含抗体主要识别末端Galα1-3Gal-R,壳三糖和Fucα1-2Galβ1-4GlcNAc-R(H型2)。流行性感冒感染后,聚糖阵列分析显示,可识别聚糖的抗体的水平和组成均下降。但是,通过ELISA进行的血清分析表明,流感病毒感染后,针对特定聚糖抗原的抗聚糖Abs不同同种型的水平增加,这表明聚糖抗原的呈递和Abs的同种型是关键的参数。测量抗多糖抗体时要考虑到这一点。禽流感研究中的这种新方法可能有助于开发广谱疫苗,并提高我们对聚糖的先天和适应性反应的机制理解。

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