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通过DNA免疫的替代方法增强对流感病毒血凝素蛋白的黏膜免疫反应。

Enhancement of mucosal immune responses to the influenza virus HA protein by alternative approaches to DNA immunization.

作者信息

Sha Z, Vincent M J, Compans R W

机构信息

Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322, USA.

出版信息

Immunobiology. 1999 Feb;200(1):21-30. doi: 10.1016/S0171-2985(99)80030-8.

Abstract

DNA immunization provides many advantages as an approach to prevent infectious diseases. However, although previous studies using this approach have demonstrated immune responses in serum, they were not successful in inducing significant levels of antibodies in secretions. In this study, plasmid DNAs expressing the influenza virus hemagglutinin glycoprotein have been evaluated for their ability to induce antibody responses in serum and saliva when used alone or along with either liposomes or bioadhesive polymers as mucosal delivery vehicles. Significant levels of virus-specific Ig in serum as well as secretory IgA in saliva were detected in mice following mucosal DNA immunization. These antibodies were found to block the infectivity of the virus using a plaque reduction assay. Our findings thus indicate that mucosal DNA immunization with specific delivery systems can elicit virus-specific antibody responses in serum as well as IgA responses at mucosal surfaces.

摘要

DNA免疫作为一种预防传染病的方法具有诸多优势。然而,尽管此前使用该方法的研究已在血清中证实了免疫反应,但在诱导分泌物中产生显著水平的抗体方面却未取得成功。在本研究中,对表达流感病毒血凝素糖蛋白的质粒DNA进行了评估,以确定其单独使用或与脂质体或生物黏附聚合物作为黏膜递送载体联合使用时,诱导血清和唾液中抗体反应的能力。黏膜DNA免疫后,在小鼠血清中检测到了显著水平的病毒特异性Ig,在唾液中检测到了分泌型IgA。通过蚀斑减少试验发现,这些抗体能够阻断病毒的感染性。因此,我们的研究结果表明,使用特定递送系统进行黏膜DNA免疫可在血清中引发病毒特异性抗体反应,并在黏膜表面引发IgA反应。

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