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首页> 外文期刊>Vaccine >Intranasal administration of a flagellin-adjuvanted inactivated influenza vaccine enhances mucosal immune responses to protect mice against lethal infection.
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Intranasal administration of a flagellin-adjuvanted inactivated influenza vaccine enhances mucosal immune responses to protect mice against lethal infection.

机译:经鼻内施用鞭毛蛋白佐剂的灭活流感疫苗可增强粘膜免疫反应,从而保护小鼠免受致命感染。

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The influenza virus, a mucosal pathogen that infects the respiratory tract, is a major global health issue. There have been attempts to mucosally administer inactivated influenza vaccines to induce both mucosal and systemic immune responses. However, mucosally administered inactivated influenza vaccine has low immunogenicity, which is partially due to the lack of an effective mucosal adjuvant. The development of a safe and effective mucosal adjuvant is a prerequisite to the practical use of a mucosal inactivated influenza vaccine. We have previously demonstrated that a bacterial flagellin, Vibrio vulnificus FlaB, when mixed with antigen and administered intranasally, exerts a strong mucosal adjuvant activity by stimulating the Toll-like receptor 5 (TLR5). In this study, we tested whether the FlaB protein could serve as an effective mucosal adjuvant for an inactivated trivalent influenza vaccine (TIV) manufactured for humans; in a murine vaccination model, this vaccine consists of A/Brisbane/59/07 (H1N1 subtype), A/Uruguay/716/07 (H3N2 subtype), and B/Florida/4/06 (B type). Intranasal co-administration of the TIV with FlaB induced prominent humoral responses as demonstrated by high influenza-specific IgA levels in both the mucosal secretions and serum and significant specific IgG induction in the systemic compartment. The FlaB protein significantly potentiated influenza-specific cytokine production by draining lymph node cells and splenocytes. The FlaB mucosal adjuvant conferred excellent protection against a lethal challenge with a live virulent virus with high hemagglutination inhibition (HAI) antibody (Ab) titers. The FlaB did not accumulate in the olfactory nerve and epithelium, guaranteeing against a retrograde uptake into the central nervous system. These results suggest that FlaB can be used as a promising mucosal adjuvant for nasal inactivated influenza vaccine development.Digital Object Identifier http://dx.doi.org/10.1016/j.vaccine.2011.10.058
机译:流感病毒是一种感染呼吸道的粘膜病原体,是全球主要的健康问题。已经尝试过粘膜施用灭活的流感疫苗以诱导粘膜和全身免疫应答。然而,经粘膜施用的灭活流感疫苗具有低免疫原性,部分原因是缺乏有效的粘膜佐剂。安全有效的粘膜佐剂的开发是粘膜灭活流感疫苗实际使用的前提。先前我们已经证明,细菌鞭毛蛋白创伤弧菌FlaB,当与抗原混合并经鼻内给药时,可通过刺激Toll样受体5(TLR5)发挥强大的粘膜佐剂活性。在这项研究中,我们测试了FlaB蛋白是否可以作为为人类生产的灭活三价流感疫苗(TIV)的有效粘膜佐剂;在鼠类疫苗接种模型中,该疫苗由A /布里斯班/ 59/07(H1N1亚型),A /乌拉圭/ 716/07(H3N2亚型)和B /佛罗里达/ 4/06(B型)组成。 TIV与FlaB的鼻内联合给药可引起显着的体液反应,如粘膜分泌物和血清中高流感特异性IgA水平和全身区室中明显的特异性IgG诱导所证明。 FlaB蛋白通过排干淋巴结细胞和脾细胞显着增强了流感特异性细胞因子的产生。 FlaB粘膜佐剂可对具有高血凝抑制(HAI)抗体(Ab)滴度的活泼强毒病毒提供极好的保护,使其免受致命性攻击。 FlaB不会在嗅觉神经和上皮细胞中积聚,从而确保不会逆行摄取到中枢神经系统中。这些结果表明,FlaB可以用作鼻灭活流感疫苗开发的有希望的粘膜佐剂。数字对象标识符http://dx.doi.org/10.1016/j.vaccine.2011.10.058

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