B. Maecker, M.S. von Bergwelt-Baildon, K.S. Anderson, R.H. Vonderheide and J.L. Schultze Pages 609 - 619 ( 11 )
The disclosure of the human genome sequence and rapid advances in genomic expression profiling have revolutionized our knowledge about molecular changes in malignant diseases. Rapidly growing gene expression databases and improvements in bioinformatics tools set the stage for new approaches using large-scale molecular information to develop specific therapeutics in cancer. On one hand, the ability to detect clusters of genes differentially expressed in normal and malignant tissue may lead to widely applicable targeting of defined molecular structures. On the other hand, analyzing the ‘molecular fingerprint’ of an individual tumor raises the possibility of developing customized therapeutics. One approach to use the emerging new datasets for the development of novel therapeutics is to identify genes that are specifically expressed in tumors as targets for immune intervention. This review will focus on the process from in silico analysis of expression databases and screening of potential candidate genes by bioinformatics to the in vitro and in vivo analysis to determine the immunogenicity of candidate tumor antigens. Basic biological principles of ‘reverse immunology’ as well as technical advantages and difficulties will be addressed., Linking, Genomics, to, Immunotherapy, by, Reverse, Immunology, -, ‘Immunomics’, in, the, New, Millennium
Department of Adult Oncology, Dana-Farber Cancer Institute, 44 Binney Street, D540C, Boston, MA 02115, USA.