Clark R E, Dodi I A, Hill S C, Lill J R, Aubert G, Macintyre A R, Rojas J, Bourdon A, Bonner P L, Wang L, Christmas S E, Travers P J, Creaser C S, Rees R C, Madrigal J A
Department of Life Sciences and Chemistry and Physics, Nottingham Trent University, Nottingham, United Kingdom.
Blood. 2001 Nov 15;98(10):2887-93. doi: 10.1182/blood.v98.10.2887.
The BCR-ABL oncogene is central in the pathogenesis of chronic myeloid leukemia (CML). Here, tandem nanospray mass spectrometry was used to demonstrate cell surface HLA-associated expression of the BCR-ABL peptide KQSSKALQR on class I-negative CML cells transfected with HLA-A*0301, and on primary CML cells from HLA-A3-positive patients. These patients mounted a cytotoxic T-lymphocyte response to KQSSKALQR that also killed autologous CML cells, and tetramer staining demonstrated the presence of circulating KQSSKALQR-specific T cells. The findings are the first demonstration that CML cells express HLA-associated leukemia-specific immunogenic peptides and provide a sound basis for immunization studies against BCR-ABL.
BCR-ABL致癌基因在慢性粒细胞白血病(CML)的发病机制中起核心作用。在此,串联纳米喷雾质谱法被用于证明在转染了HLA-A*0301的I类阴性CML细胞以及来自HLA-A3阳性患者的原发性CML细胞表面,BCR-ABL肽KQSSKALQR与HLA相关的表达。这些患者对KQSSKALQR产生了细胞毒性T淋巴细胞反应,该反应也杀死了自体CML细胞,并且四聚体染色证明存在循环的KQSSKALQR特异性T细胞。这些发现首次证明CML细胞表达与HLA相关的白血病特异性免疫原性肽,并为针对BCR-ABL的免疫研究提供了坚实的基础。