Development of avian influenza virus H5 DNA vaccine and MDP-1 gene of Mycobacterium bovis as genetic adjuvant.

Babak Jalilian, Abdul Rahman Omar, Mohd Hair Bejo, Noorjahan Banu Alitheen, Mehdi Rasoli, Sohkichi Matsumoto
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引用次数: 22

Abstract

Background: Studies have shown that DNA vaccines can induce protective immunity, which demonstrated the high potential of DNA vaccines as an alternative to inactivated vaccines. Vaccines are frequently formulated with adjuvants to improve their release, delivery and presentation to the host immune system.

Methods: The H5 gene of H5N1 virus (A/Ck/Malaysia/5858/04) was cloned separately into pcDNA3.1 + vector. The immunogenicity of the cloned H5 DNA vaccine was tested on SPF chickens using two different approaches. First approach was using H5 DNA vaccine (pcDNA3.1/H5) and the second was using H5 DNA vaccine in addition to the pcDNA3.1/MDP1 vaccine. Ten days old chickens inoculated three times with two weeks intervals. The spleen and muscle samples from chickens immunized with H5 (pcDNA3.1/H5) and H5 + MDP1 (pcDNA3.1/H5 + pcDNA3.1/MDP1) vaccines were collected after sacrificing the chickens and successfully expressed H5 and MDP1 RNA transcripts. The sera of immunized chickens were collected prior to first immunization and every week after immunization; and analyzed using enzyme-linked immunosorbent assay (ELISA) and hemagglutination inhibition (HI) test.

Results: Results of competitive ELISA showed successful antibody responses two weeks post immunization. The HI test showed an increased in antibody titers during the course of experiment in group immunized with H5 and H5 + MDP1 vaccines. The result showed that the constructed DNA vaccines were able to produce detectable antibody titer in which the group immunized with H5 + MDP1 vaccine produced higher antibody comparing to H5 vaccine alone.

Conclusions: This study shows for the first time the usefulness of MDP1 as a genetic adjuvant for H5 DNA vaccine.

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禽流感病毒H5 DNA疫苗及牛分枝杆菌MDP-1基因作为遗传佐剂的研制。
背景:研究表明DNA疫苗可以诱导保护性免疫,这表明DNA疫苗作为灭活疫苗的替代品具有很高的潜力。疫苗通常与佐剂配制,以改善其释放,传递和呈现给宿主免疫系统。方法:将H5N1病毒H5基因(A/Ck/Malaysia/5858/04)分别克隆到pcDNA3.1 +载体上。用两种不同的方法对克隆的H5 DNA疫苗的免疫原性进行了测试。第一种方法是使用H5 DNA疫苗(pcDNA3.1/H5),第二种方法是在pcDNA3.1/MDP1疫苗的基础上使用H5 DNA疫苗。10天大的鸡接种三次,间隔两周。用H5 (pcDNA3.1/H5)和H5 + MDP1 (pcDNA3.1/H5 + pcDNA3.1/MDP1)疫苗免疫鸡后,宰杀鸡采集脾脏和肌肉标本,成功表达H5和MDP1 RNA转录物。免疫鸡在第一次免疫前和免疫后每周采集血清;采用酶联免疫吸附试验(ELISA)和血凝抑制试验(HI)进行分析。结果:竞争性ELISA结果显示免疫后2周抗体应答成功。H5和H5 + MDP1疫苗免疫组在实验过程中抗体滴度升高。结果表明,构建的DNA疫苗能够产生可检测的抗体效价,其中H5 + MDP1疫苗免疫组比单独H5疫苗免疫组产生更高的抗体效价。结论:本研究首次证明了MDP1作为H5 DNA疫苗的遗传佐剂的有效性。
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