Erschienen in:
01.06.2003 | Symposium Series
International conference: Progress in vaccination against cancer (PIVAC) 2002, Nottingham, UK
verfasst von:
Robert C. Rees, R. Adrian Robins, Graham Pawelec, Ludmila Muller, Geng Li, Ian Spendlove
Erschienen in:
Cancer Immunology, Immunotherapy
|
Ausgabe 6/2003
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Excerpt
Applying new methods for detecting and quantifying responses to tumour antigens is essential for accurate evaluation of patients undergoing immunotherapy. A good example of these new approaches is MHC tetramer technology, where T cells recognizing a particular MHC-peptide combination can be identified and counted by their binding of labelled tetrameric MHC-peptide complexes. This was illustrated by A. Dodi (London) in patients with chronic myelogenous leukaemia (CML). There is an "ideal" candidate antigen in CML represented by the bcr/abl fusion protein resulting from the presence of the Philadelphia chromosome. Tetramer-positive cells, recognising the HLA-A* 0301-restricted peptide KQSSKALQR which is uniquely associated with the fusion sequence, can be detected in patients. CD8
+ T cells expand in response to peptide in vitro and are able to recognise and kill CML cells that express the bcr/abl fusion peptide, illustrating its importance as a target for immunotherapy [
4]. …