Departments of Respiratory Medicine and Clinical Immunology.
Cancer Stem Cell Biology.
J Immunother. 2022 Jan 1;45(1):56-66. doi: 10.1097/CJI.0000000000000405.
The HLA-A*24:02-restricted peptide vaccine targeting Wilms' tumor 1 (WT1) (WT1 vaccine) is a promising therapeutic strategy for ovarian cancer; however, its efficacy varies among patients. In this study, we analyzed WT1-specific immune responses in patients with advanced or recurrent ovarian cancer that was refractory to standard chemotherapies and their associations with clinical outcomes. In 25 patients, the WT1 vaccine was administered subcutaneously weekly for 3 months and biweekly thereafter until disease progression or severe adverse events. We assessed Wilms' tumor 1-specific cytotoxic T lymphocytes (WT1-CTLs) and Wilms' tumor 1 peptide-specific immunoglobulin G (WT1235-IgG). After vaccination, the percentage of tetramer high-avidity population of WT1-CTLs among CD8+ T lymphocytes (%tet-hi WT1-CTL) and the WT1235-IgG titer increased significantly, although the values were extremely low or below the limit of detection before vaccination (%tet-hi WT1-CTL: 0.003%-0.103%.; WT1235-IgG: <0.05-0.077 U/mL). Patients who had %tet-hi WT1-CTL of ≥0.25% (n=6) or WT1235-IgG of ≥0.10 U/mL (n=12) had a significantly longer progression-free survival than those of patients in the other groups. In addition, an increase in WT1235-IgG corresponded to a significantly longer progression-free survival (P=0.0496). In patients with systemic inflammation, as evidenced by elevated C-reactive protein levels, the induction of tet-hi WT1-CTL or WT1235-IgG was insufficient. Decreased serum albumin levels, multiple tumor lesions, poor performance status, and excess ascites negatively influenced the clinical effectiveness of the WT1 vaccine. In conclusion, the WT1 vaccine induced antigen-specific cellular and humoral immunity in patients with refractory ovarian cancer. Both %tet-hi WT1-CTL and WT1235-IgG levels are prognostic markers for the WT1 vaccine.
靶向 Wilms 瘤 1(WT1)的 HLA-A*24:02 限制性肽疫苗(WT1 疫苗)是一种有前途的卵巢癌治疗策略;然而,其疗效在患者之间存在差异。在这项研究中,我们分析了对标准化疗耐药的晚期或复发性卵巢癌患者的 WT1 特异性免疫反应及其与临床结局的关系。在 25 例患者中,WT1 疫苗每周皮下注射一次,持续 3 个月,此后每两周一次,直到疾病进展或出现严重不良事件。我们评估了 Wilms 瘤 1 特异性细胞毒性 T 淋巴细胞(WT1-CTL)和 Wilms 瘤 1 肽特异性免疫球蛋白 G(WT1235-IgG)。接种疫苗后,CD8+T 淋巴细胞中四聚体高亲和力群体的 WT1-CTL 的百分比(%tet-hi WT1-CTL)和 WT1235-IgG 滴度显著增加,尽管接种疫苗前这些值极低或低于检测限(%tet-hi WT1-CTL:0.003%-0.103%;WT1235-IgG:<0.05-0.077 U/mL)。%tet-hi WT1-CTL 为≥0.25%(n=6)或 WT1235-IgG 为≥0.10 U/mL(n=12)的患者的无进展生存期显著长于其他组的患者。此外,WT1235-IgG 的增加与无进展生存期显著延长相关(P=0.0496)。在存在全身性炎症的患者中,如 C 反应蛋白水平升高所证明的,高亲和力的四聚体 WT1-CTL 或 WT1235-IgG 的诱导不足。血清白蛋白水平降低、多发肿瘤病变、较差的表现状态和大量腹水对 WT1 疫苗的临床疗效有负面影响。总之,WT1 疫苗在耐药性卵巢癌患者中诱导了抗原特异性细胞和体液免疫。%tet-hi WT1-CTL 和 WT1235-IgG 水平均是 WT1 疫苗的预后标志物。