Journal of Clinical and Cellular Immunology
Open Access
ISSN: 2155-9899
ISSN: 2155-9899
Andreas Weinhaeusel
AIT Austrian Institute of Technology GmbH, Austria
Keynote: J Clin Cell Immunol
An individualâ��s antibody profile or immunome is stable over years but can change in respect to pathological changes as well as these changes can be triggered by vaccination/ immunization or different therapeutic intervention. Antibody profiling on high density protein and peptide arrays has been shown to elucidate pathophysiological alterations in various indications like autoimmune, cancerous, and neurological disease, as well as in allergy and infectious disease. Protein-arrays are usually generated using recombinant expression, and have limited flexibility â�� but can be customized when proteins are available. Peptide-arrays can be easily customized to present proteins deduced from sequences, without the need of protein-expression. We have set up immunomics discovery technologies using protein- and peptide-microarrays (presenting 32000 spots or up to 6 mio peptides, respectively) as well as targeted multiplexed technologies for validation of findings. These are all customizable and affordable even when discovery studies are done with a small number of samples. In line with the different technologies we have established and optimized bioinformatics and laboratory methods and can provide complete workflows from design, experimental setup and sample analysis till data-analysis. This is also true when we have lower multi-plexed technologies available providing targeted micro-arrays (presenting hundred thousand antigens) as well as bead-arrays in an up to 500-plexed format for marker-refinement and confirmation. For broader validation and clinical studies we have both micro- and bead-array technologies established for analyzing large series of samples in 96-well microtiter-plates in medium-plexed assays. We have established and optimized different methods and combined these to a full workflow for providing modules as well as the entire pipeline for antibody-based analysis and diagnostics, which can be conducted with 10�¼l amounts of serum or plasma as well as using other body fluids like saliva.
Andreas Weinhaeusel by his profession is a Biotechnologist and Associate Professor for Molecular Biology at the University of Natural Resources and Applied Life Sciences, Vienna. During 1995-2004 he worked at the Children’s Cancer Research Institute, Vienna and he is experienced in human molecular genetic diagnostics and specialized on diagnostic-testing of syndromal and hereditary neoplastic disease. In 2001, he obtained the Post-doctoral graduation specialist in Human Genetics. Since 2004, he is working at the Molecular Diagnostics Business-unit of the AIT-Austrian Institute of Technology. He is specialized on DNA-methylation and autoantibody biomarker development using microarray and high throughput technologies.