医学
鼻咽癌
细胞毒性T细胞
免疫学
免疫系统
CD8型
爱泼斯坦-巴尔病毒
免疫疗法
抗原
T细胞
病毒
放射治疗
内科学
生物
体外
生物化学
作者
Patrizia Comoli,Paolo Pedrazzoli,Rita Maccario,Sabrina Basso,Ornella Carminati,Massimo Labirio,Roberta Schiavo,Simona Secondino,Chiara Frasson,Cesare Perotti,Mauro Moroni,Franco Locatelli,Salvatore Siena
标识
DOI:10.1200/jco.2005.02.6195
摘要
Purpose Nasopharyngeal carcinoma (NPC) is an Epstein-Barr virus (EBV) –related malignancy expressing EBV antigens that are possible targets of cell therapy, including latent membrane protein 2 (LMP2). We conducted a clinical trial of EBV-targeted cell therapy with autologous virus-specific cytotoxic T lymphocytes (CTLs) for NPC refractory to conventional treatments. Patients and Methods Ten patients with EBV-related stage IV NPC in progression after conventional radiotherapy and chemotherapy received intravenously autologous EBV-specific CTLs reactivated and expanded ex vivo from peripheral blood lymphocytes through stimulation with EBV-transformed autologous B-lymphoblastoid cell lines (LCL). Toxicity, specific cellular immune responses, and clinical tumor responses were evaluated. Results EBV-specific CTLs could be generated in all patients and were predominantly CD3 + /CD8 + T lymphocytes displaying specific killing of autologous EBV-LCL, autologous NPC cells as well as autologous targets bearing the EBV antigen LMP2. Patients received two to 23 infusions of EBV-specific CTLs that were well tolerated with the exception of grade 1 to 2 inflammatory reactions at the tumor site in two cases. Control of disease progression was obtained in six of 10 patients (two with partial response and four with stable disease). Analysis of interferon-γ–producing cells demonstrated an increased frequency of EBV-specific immunity, with appearance of LMP2-specific responses in four patients, of whom three had clinical benefit. Conclusion Cell therapy with EBV-targeted autologous CTLs is safe, induces LMP-2-specific immunologic responses, and is associated with objective responses and control of disease progression in patients with stage IV NPC resistant to conventional treatments.
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