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DNA 疫苗编码禽流感病毒 H5 和结核分枝杆菌 Esat-6 可提高鸡对 AIV 的抗体反应。

DNA vaccine encoding avian influenza virus H5 and Esat-6 of Mycobacterium tuberculosis improved antibody responses against AIV in chickens.

机构信息

Institute of Bioscience, University Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia.

出版信息

Comp Immunol Microbiol Infect Dis. 2010 Dec;33(6):491-503. doi: 10.1016/j.cimid.2009.08.004. Epub 2009 Sep 24.

Abstract

The H5 gene of avian influenza virus (AIV) strain A/chicken/Malaysia/5744/2004(H5N1) was cloned into pcDNA3.1 vector, and Esat-6 gene of Mycobacterium tuberculosis was fused into downstream of the H5 gene as a genetic adjuvant for DNA vaccine candidates. The antibody level against AIV was measured using enzyme-linked immunosorbent assay (ELISA) and haemagglutination inhibition (HI) test. Sera obtained from specific-pathogen-free chickens immunized with pcDNA3.1/H5 and pcDNA3.1/H5/Esat-6 demonstrated antibody responses as early as 2 weeks after the first immunization. Furthermore, the overall HI antibody titer in chickens immunized with pcDNA3.1/H5/Esat-6 was higher compared to the chickens immunized with pcDNA3.1/H5 (p<0.05). The results suggested that Esat-6 gene of M. tuberculosis is a potential genetic adjuvant for the development of effective H5 DNA vaccine in chickens.

摘要

禽流感病毒(AIV)株 A/鸡/马来西亚/5744/2004(H5N1)的 H5 基因被克隆到 pcDNA3.1 载体中,结核分枝杆菌的 Esat-6 基因被融合到 H5 基因的下游,作为 DNA 疫苗候选物的遗传佐剂。使用酶联免疫吸附试验(ELISA)和血凝抑制(HI)试验测量针对 AIV 的抗体水平。用 pcDNA3.1/H5 和 pcDNA3.1/H5/Esat-6 免疫的无特定病原体鸡的血清在首次免疫后 2 周即可产生抗体反应。此外,用 pcDNA3.1/H5/Esat-6 免疫的鸡的总体 HI 抗体滴度高于用 pcDNA3.1/H5 免疫的鸡(p<0.05)。结果表明,结核分枝杆菌的 Esat-6 基因是开发鸡用有效 H5 DNA 疫苗的潜在遗传佐剂。

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