接受HLA-Cw*0702相关表位MAGE-A12:170-178免疫治疗的转移性黑色素瘤患者的临床和免疫学评估
Clinical and immunological evaluation of patients with metastatic melanoma undergoing immunization with the HLA-Cw*0702-associated epitope MAGE-A12:170-178.
作者信息
Bettinotti Maria P, Panelli Monica C, Ruppe Erin, Mocellin Simone, Phan Giao Q, White Donald E, Marincola Francesco M
机构信息
Department of Transfusion Medicine, Clinical Center, National Institutes of Health, Bethesda, MD 20892, USA.
出版信息
Int J Cancer. 2003 Jun 10;105(2):210-6. doi: 10.1002/ijc.11045.
Patients with metastatic melanoma who expressed HLA-Cw0702 and whose tumors had demonstrable MAGE-A12 expression were immunized with the peptide MAGE-A12:170-178 administered subcutaneously in incomplete Freund's adjuvant (IFA). The peptide was administered either every week or every 3 weeks for 4 cycles. Patients were evaluated for toxicity and for immunologic and clinical response to peptide immunization. Pre-treatment fine needle aspirates were obtained to document MAGE-A12 expression for enrollment. MAGE-A12 mRNA was identified in 62% of specimens. Nine patients were selected for vaccination based on MAGE-A12 expression and the presence of HLA-Cw0702. The immune response was monitored both by tetrameric HLA-Cw*0702/MAGE-A12:170-178 complexes and by analysis of interferon-gamma mRNA transcription using a quantitative real-time polymerase chain reaction assay after peptide-specific stimulation. The samples consisted of circulating lymphocytes analyzed ex vivo or after 10 to 14 days of in vitro sensitization. One of 9 patients sustained an ongoing partial clinical response. No convincing evidence of enhancement of the systemic immune response against MAGE-A12:170-178 could be documented. Because of the modest immunological and clinical results, the present protocol has been discontinued as new routes of administration are being considered.
表达HLA - Cw0702且肿瘤有可检测到的MAGE - A12表达的转移性黑色素瘤患者,用肽MAGE - A12:170 - 178皮下注射免疫,佐剂为不完全弗氏佐剂(IFA)。肽每周或每3周给药1次,共4个周期。对患者进行毒性评估以及对肽免疫的免疫和临床反应评估。获取治疗前细针穿刺抽吸物以记录MAGE - A12表达用于入组。62%的标本中鉴定出MAGE - A12 mRNA。基于MAGE - A12表达和HLA - Cw0702的存在选择9例患者进行疫苗接种。通过四聚体HLA - Cw*0702/MAGE - A12:170 - 178复合物以及在肽特异性刺激后使用定量实时聚合酶链反应测定法分析干扰素 - γ mRNA转录来监测免疫反应。样本包括离体分析的循环淋巴细胞或体外致敏10至14天后的淋巴细胞。9例患者中有1例持续有部分临床反应。没有可记录的令人信服的证据表明针对MAGE - A12:170 - 178的全身免疫反应增强。由于免疫和临床结果不显著,随着正在考虑新的给药途径,目前的方案已停止。