Generation of antibodies by genetic immunization
Generation of antibodies by genetic immunization
批准号:
6485127
负责人:
Hans Herweijer
金额:
$10.91万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-04-01 至 2002-11-30
关键词:
DNA antibody flow cytometry gene delivery system gene expression humoral immunity immunocytochemistry immunogenetics immunologic substance development /preparation laboratory mouse liver cells luciferin monooxygenase passive immunization plasmids tissue /cell culture transfection /expression vector western blottings
中文摘要
说明:(申请人提供)基因免疫提供专业
英文摘要
DESCRIPTION: (Provided by Applicant) Genetic immunization provides major
advantages over classic protein/peptide immunization for the generation of
antigen-specific antibodies. In vivo expression of the antigen following gene
transfer results in proper modification and folding, and thus presentation of
natural epitopes. For many antigen candidates, no purified protein is available
and peptide synthesis is not always feasible. To efficiently enable the
generation of useful antibodies via genetic immunization methods, two technical
hurdles need to be overcome, First, one needs to be able to screen for the
presence of the antibodies in the sera of genetically immunized mice, without
the availability of antigen. This problem can be solved by expressing the
antigen from plasmid DNA expression vectors after in vitro or in vivo
high-efficiency gene transfer. Cells expressing the antigen can be used in
immunohistochemistry, flow cytometry, or Western blotting analysis to identify
antigen-specific antibodies. Second, efficient, simple, and cost effective in
vivo gene transfer is required to induce a humoral immune response. Mirus'
intravascular plasmid DNA gene transfer methods fulfill these requirements and
can efficiently induce antibody responses against expressed transgenes.
In this Phase I application, we propose to determine which intravascular gene
transfer method result in the most efficient humoral immune response against
different classes of expressed antigens. We will also optimize Western blotting
antibody screening methods by expressing antigens in different cell lines and
in liver cells. During the Phase II studies, we will further optimize genetic
immunization methods by including cytokine genes, refining the immunization
schedule, and testing different expression vectors and mouse strains. The
screening methods will be improved by testing pooling of sera (to limit the
initial number of assays), and testing other assays (immunohistochemistry, flow
cytometry, ELISA). This technology will allow Mirus to provide a comprehensive
antibody generation service, identify novel antibodies for the research market
as well as for therapeutic targets, and introduce genetic immunization and
antibody screening kits.
PROPOSED COMMERCIAL APPLICATION: NOT AVAILABLE
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
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海外基金