2012Jiguang shengwu xuebaoRequires access

Immune Effect of DNA Prime-Protein Boost Immune Strategy Based on H9N2 Avian Influenza Virus Matrix Protein 2

Chang Haiyan

Open publisher page 0 citations

Abstract

Influenza matrix protein 2(M2) is highly conserved in influenza A viruses.Considering the low immunogenicity of M2,DNA prime-protein boost immunization strategy was explored to improve the immune effect in our study.The M2 DNA plasmid and the sM2 protein(i.e.M2 protein without transmembrane domain expressed in E.coli) from avian influenza virus A/Chicken/Jiangsu/7/2002(H9N2) were prepared.The M2 DNA was intramuscularly injected into BALB/c mice by electroporation,and the sM2 protein was administered to mice by nasal dropping.The immunization interval was 3 weeks.Three weeks after the last immunization,the mice were challenged with lethal(5LD50) homologous virus.The effects of various immune strategies were evaluated by survival rate,body weight change,lung virus titer and the M2-specific IgG antibody levels in mice.The results showed that,compared with the unimmunized mice,M2 DNA prime + protein boost twice could provide complete protection for mice against lethal homologous virus challenge.

About this research paper

What this paper is about

Influenza matrix protein 2(M2) is highly conserved in influenza A viruses.Considering the low immunogenicity of M2,DNA prime-protein boost immunization strategy was explored to improve the immune effect in our study.The M2 DNA plasmid and the sM2 protein(i.e.M2 protein without transmembrane domain expressed in E.coli) from avian influenza virus A/Chicken/Jiangsu/7/2002(H9N2) were prepared.The M2 DNA was intramuscularly injected into BALB/c mice by electroporation,and the sM2 protein was administered to mice by nasal dropping.The immunization interval was 3 weeks.Three weeks after the last immunization,the mice were challenged with lethal(5LD50) homologous virus.The effects of various immune strategies were evaluated by survival rate,body weight change,lung virus titer and the M2-specific IgG antibody levels in mice.The results showed that,compared with the unimmunized mice,M2 DNA prime + protein boost twice could provide complete protection for mice against lethal homologous virus challenge.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Influenza matrix protein 2(M2) is highly conserved in influenza A viruses.Considering the low immunogenicity of M2,DNA prime-protein boost immunization strategy was explored to improve the immune effect in our study.The M2 DNA plasmid and the sM2 protein(i.e.M2 protein without transmembrane domain expressed in E.coli) from avian influenza virus A/Chicken/Jiangsu/7/2002(H9N2) were prepared.The M2 DNA was intramuscularly injected into BALB/c mice by electroporation,and the sM2 protein was administered to mice by nasal dropping.The immunization interval was 3 weeks.Three weeks after the last immunization,the mice were challenged with lethal(5LD50) homologous virus.The effects of various immune strategies were evaluated by survival rate,body weight change,lung virus titer and the M2-specific IgG antibody levels in mice.The results showed that,compared with the unimmunized mice,M2 DNA prime + protein boost twice could provide complete protection for mice against lethal homologous virus challenge.

Key concepts: Immunogenicity, Viral matrix protein, Virology, Virus, DNA vaccination, Biology, Immune system, Influenza A virus subtype H5N1

Related papers

Back to paper searchBrowse research topicsOriginal source
Immune Effect of DNA Prime-Protein Boost Immune Strategy Based on H9N2 Avian Influenza Virus Matrix Protein 2 — Research Paper | ScholarLens