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A peptide encoded by the human MAGE3 gene and presented by HLA-1344 induces cytolytic T lymphocytes that recognize tumor cells expressing MAGE3
Authors:Jean Herman  Pierre van der Bruggen  Immanuel F Luescher  Susanna Mandruzzato  Pedro Romero  Joëlle Thonnard  Katharina Fleischhauer  Thierry Boon  Pierre G Coulie
Institution:(1) Ludwig Institute for Cancer Research, 74 avenue Hippocrate, UCL 74.59 B-1200 Brussels, Belgium;(2) Cellular Genetics Unit, Université Catholique de Louvain, Brussels, Belgium;(3) Ludwig Institute for Cancer Research, Lausanne Branch, and University of Lausanne, 1066 Epalinges, Switzerland;(4) Laboratoire de Biologie Moléculaire Clinique, Cliniques Universitaires Saint Luc, Brussels, Belgium;(5) Laboratory of Experimental Hematology, DIBIT, Istituto Scientifico H. S. Raffaele, 20132 Milano, Italy
Abstract:The humanMAGE3 gene is expressed in a significant proportion of tumors of various histological types, but is silent in normal adult tissues other than testis and placenta. Antigens encoded byMAGE3 may therefore be useful targets for specific antitumor immunization. Two antigenic peptides encoded by theMAGE3 gene have been reported previously. One is presented to cytolytic T lymphocytes (CTL) by HLA-A1, the other by HLA-A2 molecules. Here we show that MAGE3 also codes for a peptide that is presented to CTL by HLA-1344.MAGE3 peptides containing the HLA-1344 peptide binding motif were synthesized. Peptide MEVDPIGHLY, which showed the strongest binding to HLA-1344, was used to stimulate blood T lymphocytes from normal HLA-1344 donors. CTL clones were obtained that recognized not only HLA-B44 cells sensitized with the peptide, but also HLA-B44 tumor cell lines expressingMAGE3. The proportion of metastatic melanomas expressing theMAGE3/HLA-1344 antigen should amount to approximately 17% in the Caucasian population, since 24% of individuals carry theHLA-B44 allele and 76% of these tumors express MAGE3.
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