Enhancement of protection against various microbial infection by the modification of dominance of Thl or Th2 immune responses
Enhancement of protection against various microbial infection by the modification of dominance of Thl or Th2 immune responses
批准号:
11470070
负责人:
OKUDA Kenji
金额:
$9.79万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
1999
资助国家:
日本
项目状态:
已结题
起止时间:
1999 至 2001
中文摘要
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英文摘要
An experiment was conducted to test the possibility of protection inducement by a new type of DNA vaccine against Pseudomonas, HIV and influenza virus infection. The vaccine was constructed by inserting genes, which code the various protective antigens of the pathogenic organism. In addition, we synthesized DNA by using humanized codons.For the HIV vaccine, an examination was conducted to check the efficacy, immunogenicity and safety according to the method of medication. In order to do this the 18 genes that code HIV-1 antigenic epitopes, each made of about 15 amino acids, were connected in series. Investigations were made as to whether administrating DNA vaccine to pregnant animals will induce a higher immunogenicity in the offspring due to placental penetration. Results suggesting a possibility of higher immunogenicity in the offspring were obtained. Moreover, varying the administration method of the DNA vaccine by i.e. oral, intranasal, percutaneous, intravenous and rectal showed different results in mucosal, local and systemic immunities. In the research of the influenza virus vaccine, with the view to activate the CTL response,we constructed M gene plasmid that expresses the M protein which is the core of the virus. This DNA vaccine was revealed to be effective against the challenge using various influenza viruses. These results are highly suggestive that these so-called "humanized codon multivalent DNA vaccines" will be effective against various microorganisms and will be a vaccine for the next generation.
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Kusakabe K-i.: "The timing of GM-CSF expression plasmid administration influences the Th1/Th2 response induced by an HIV-1 specific DNA vaccine"J.Immunol.. 164・6. 3102-3111 (2000)
Kusakabe K-i.:“GM-CSF表达质粒施用的时机影响HIV-1特异性DNA疫苗诱导的Th1/Th2反应”J.Immunol.. 164・6(2000)。
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Hagiwara E.: "IL-12-encoding plasmid has a beneficial effect on spontaneous autoimmune disease in MRL/MP-lpr/lpr mice"Cytokine. 18. 1035-1041 (2000)
Hagiwara E.:“IL-12 编码质粒对 MRL/MP-lpr/lpr 小鼠的自发性自身免疫性疾病具有有益作用”细胞因子。
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Kawamoto S.: "Methods in Molecular Biology "NMDA Receptor Protocols", Expression of NMDA receptor channel subunit proteins using baculovirus and herpesvirus vectors"Humana Press Inc., Totowa, NJ., M.Li(Ed.). 19-32 (1999)
Kawamoto S.:“分子生物学方法“NMDA 受体方案”,使用杆状病毒和疱疹病毒载体表达 NMDA 受体通道亚基蛋白”Humana Press Inc.,Totowa,NJ.,M.Li(编辑)。
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Okuda K.: "Methods in Molecular Medicine "DNA Vaccines : Methods and Protocols", Cytokine and costimulatory factor-encoding plasmids as adjunvants for DNA vaccination"Humana press, Totowa, NJ., D.B.a.W.Lowrie, R.G.(Ed.). 197-204 (1999)
Okuda K.:“分子医学方法“DNA 疫苗:方法和方案”,细胞因子和共刺激因子编码质粒作为 DNA 疫苗接种的佐剂”Humana press,Totowa,NJ.,D.B.a.W.Lowrie,R.G.(编辑)。
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Lu Y: "Macrophage inflammatory protein-1α(MEP-1α) expression plasmid enhances DNA vaccine-induced immune response against HIV-1"Clin Exp Immunol. 115(2). 335-341 (1999)
Lu Y:“巨噬细胞炎症蛋白-1α (MEP-1α) 表达质粒增强 DNA 疫苗诱导的针对 HIV-1 的免疫反应”Clin Exp Nutritionl 115(2) (1999)。
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共 74 条
Developmental research of new generation DNA vaccine against microorganism using synthesized DNA
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Study on the DNA immunization against microbial infection
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负责人:OKUDA Kenji
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依托单位:
国内基金
海外基金
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