Cancer Vaccine Center, Kurume University, Kurume 839-0863, Japan.
Department of Gastroenterology and Hepatology, Kinki University Faculty of Medicine, Osaka 589-8511, Japan.
J Immunol Res. 2015;2015:473909. doi: 10.1155/2015/473909. Epub 2015 Oct 11.
Objective. To evaluate safety and immune responses of personalized peptide vaccination (PPV) for hepatitis C virus- (HCV-) positive advanced hepatocellular carcinoma (HCC). Patients and Methods. Patients diagnosed with HCV-positive advanced HCC were eligible for this study. A maximum of four HLA-matched peptides were selected based on the preexisting IgG responses specific to 32 different peptides, which consisted of a single HCV-derived peptide at core protein positions 35-44 (C-35) and 31 peptides derived from 15 different tumor-associated antigens (TAAs), followed by subcutaneous administration once per week for 8 weeks. Peptide-specific cytotoxic T lymphocyte (CTL) and IgG responses were measured before and after vaccination. Results. Forty-two patients were enrolled. Grade 3 injection site skin reaction was observed in 2 patients, but no other PPV-related severe adverse events were noted. Peptide-specific CTL responses before vaccination were observed in only 3 of 42 patients, but they became detectable in 23 of 36 patients tested after vaccination. Peptide-specific IgG responses were also boosted in 19 of 36 patients. Peptide-specific IgG1 responses to both C-35 and TAA-derived peptides could be potentially prognostic for overall survival. Conclusion. Further clinical study of PPV would be warranted for HCV-positive advanced HCC, based on the safety and strong immune induction.
评估针对丙型肝炎病毒(HCV)阳性晚期肝细胞癌(HCC)的个体化肽疫苗(PPV)的安全性和免疫应答。
本研究纳入了诊断为 HCV 阳性晚期 HCC 的患者。根据针对 32 种不同肽的预先存在的 IgG 反应,最多选择 4 种 HLA 匹配的肽,这些肽来自核心蛋白位置 35-44(C-35)的单个 HCV 衍生肽和 15 种不同肿瘤相关抗原(TAA)的 31 种肽,随后每周皮下注射一次,共 8 周。在接种前后测量肽特异性细胞毒性 T 淋巴细胞(CTL)和 IgG 反应。
共纳入 42 例患者。2 例患者出现 3 级注射部位皮肤反应,但未观察到其他与 PPV 相关的严重不良事件。在接种前,仅 42 例患者中的 3 例观察到肽特异性 CTL 反应,但在接种后检测的 36 例患者中有 23 例可检测到。19 例患者的肽特异性 IgG 反应也得到了增强。对 C-35 和 TAA 衍生肽的肽特异性 IgG1 反应可能与总生存预后相关。
基于安全性和强烈的免疫诱导,进一步的针对 HCV 阳性晚期 HCC 的 PPV 临床研究是合理的。