Sherman W, Liu Z, Inghirami G, Reed E F, Harris P E, Suciu-Foca N M
Department of Pathology, College of Physicians and Surgeons, Columbia University, New York, N.Y. 10032.
Immunol Res. 1993;12(4):338-48. doi: 10.1007/BF02935507.
From the peripheral blood of a patient with chronic lymphocytic leukemia (CLL) we generated a T-cell line and clones which recognized autologous CLL. The line comprised T-cell clones which responded to the CLL as well as to autologous Epstein-Barr virus (EBV)-transformed B cells in an HLA-DR-restricted fashion. In addition, the line comprised clones which were CLL-specific and showed no reactivity against EBV-transformed B cells and against autologous peripheral blood mononuclear cells obtained during remission. The proliferative response of the CLL-specific T-cell clone was inhibited by monoclonal antibodies to HLA-DR11, the major histocompatibility complex (MHC)-restrictive element. These results indicate that the MHC class-II molecule of CLL binds a tumor-specific peptide which is recognized by autologous T cells in an MHC class-II-restricted fashion. Such a peptide may serve as a target for immunotherapy.
我们从一名慢性淋巴细胞白血病(CLL)患者的外周血中培养出了一个T细胞系和多个克隆,这些克隆能够识别自体CLL。该细胞系包含以HLA-DR限制方式对CLL以及自体爱泼斯坦-巴尔病毒(EBV)转化的B细胞产生反应的T细胞克隆。此外,该细胞系还包含对CLL具有特异性且对EBV转化的B细胞以及缓解期获得的自体外周血单个核细胞无反应性的克隆。针对主要组织相容性复合体(MHC)限制性元件HLA-DR11的单克隆抗体可抑制CLL特异性T细胞克隆的增殖反应。这些结果表明,CLL的MHC II类分子结合了一种肿瘤特异性肽,该肽以MHC II类限制方式被自体T细胞识别。这样一种肽可能成为免疫治疗的靶点。