Christensen Olaf, Lupu Alaviana, Schmidt Stefanie, Condomines Maud, Belle Sebastian, Maier Ariane, Hose Dirk, Neuber Brigitte, Moos Marion, Kleist Christian, Terness Peter, Ho Anthony D, Goldschmidt Hartmut, Klein Bernard, Hundemer Michael
Department of Internal Medicine V, University of Heidelberg, Heidelberg, Germany.
J Immunother. 2009 Jul-Aug;32(6):613-21. doi: 10.1097/CJI.0b013e3181a95198.
The Melan-A(aa26-35) (EAAGIGILTV) peptide is a human leukocyte antigen (HLA)-A2-restricted T-cell epitope within the Melan-A/MART-1 tumor antigen expressed on malignant melanoma cells. Melan-A and Melan-A analog (ELAGIGILTV, Melan-A(aa26-35A27L)) specific T-cells can be expanded reliably for immunotherapeutic approaches in vitro. We studied the ability of Melan-A analog (ELAGIGILTV, Melan-A(aa26-35A27L)) specific T-cells to recognize the HM1.24(aa22-30) (LLLGIGILV) peptide within the HM1.24 antigen presented by normal and malignant plasma cells. Peripheral blood mononuclear cells from HLA-A2+ healthy donors and HLA-A2+ multiple myeloma (MM) patients were stimulated with Melan-A analog peptide-loaded autologous dendritic cells, and expanded in vitro. T-cell activation was assessed by interferon-gamma specific enzyme-linked immunosorbent spot and cytotoxicity by (51)Chromium-release-assays. The frequency of Melan-A analog specific CD8+ T-cells was detected by using tetramers. Melan-A analog specific T-cells from HLA-A2+ healthy donors and HLA-A2+ MM patients showed a interferon-gamma secretion mediated by HM1.24(aa22-30) peptide-pulsed T2 cells and lysed the HLA-A2+ HM1.24+ U266 and XG-1 human myeloma derived cell-lines as well as the B-lymphoblastoid cell-line IM-9. Melan-A analog specific T-cells from MM patients specifically lysed autologous MM cells. The current data demonstrate that Melan-A analog specific T-cells crossreact with HM1.24(aa22-30). They might be a tool for the future use in immunotherapy against MM.
Melan-A(aa26 - 35)(EAAGIGILTV)肽是恶性黑色素瘤细胞上表达的Melan-A/MART-1肿瘤抗原内的一种人类白细胞抗原(HLA)-A2限制性T细胞表位。Melan-A和Melan-A类似物(ELAGIGILTV,Melan-A(aa26 - 35A27L))特异性T细胞可在体外可靠地扩增用于免疫治疗方法。我们研究了Melan-A类似物(ELAGIGILTV,Melan-A(aa26 - 35A27L))特异性T细胞识别正常和恶性浆细胞呈递的HM1.24抗原内的HM1.24(aa22 - 30)(LLLGIGILV)肽的能力。用负载Melan-A类似物肽的自体树突状细胞刺激来自HLA-A2 +健康供体和HLA-A2 +多发性骨髓瘤(MM)患者的外周血单个核细胞,并在体外扩增。通过干扰素-γ特异性酶联免疫吸附斑点法评估T细胞活化,通过(51)铬释放测定法评估细胞毒性。使用四聚体检测Melan-A类似物特异性CD8 + T细胞的频率。来自HLA-A2 +健康供体和HLA-A2 + MM患者的Melan-A类似物特异性T细胞显示出由HM1.24(aa22 - 30)肽脉冲的T2细胞介导的干扰素-γ分泌,并裂解了HLA-A2 + HM1.24 + U266和XG-1人骨髓瘤衍生细胞系以及B淋巴母细胞系IM-9。来自MM患者的Melan-A类似物特异性T细胞特异性裂解自体MM细胞。目前的数据表明,Melan-A类似物特异性T细胞与HM1.2(aa22 - 30)发生交叉反应。它们可能是未来用于抗MM免疫治疗的一种工具。