Invention Application
US20050201985A1 Modified adenoviral vectors for use in vaccines and gene therapy 审中-公开
用于疫苗和基因治疗的修饰的腺病毒载体

Modified adenoviral vectors for use in vaccines and gene therapy
Abstract:
The present invention provides novel methods and means for influencing the CTL-sensitivity of antigen presenting cells (such as dendritic cells) upon viral infections. The invention provides gene delivery vehicles useful in different therapeutic settings such as vaccination and/or gene therapy.
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