Zelba Henning, Kyzirakos Christina, Kayser Simone, Shao Borong, Reinhardt Annekathrin, Pieper Natalia, Rabsteyn Armin, Döcker Dennis, Armeanu-Ebinger Sorin, Kloor Matthias, Hadaschik Dirk, Schulze Martin, Battke Florian, Golf Alexander, Biskup Saskia
Zentrum für Humangenetik Tübingen, 72076 Tübingen, Germany.
Institut für Medizinische Genetik und Angewandte Genomik, Universitätsklinikum Tübingen, 72076 Tübingen, Germany.
Vaccines (Basel). 2024 Apr 9;12(4):397. doi: 10.3390/vaccines12040397.
Ovarian cancer is one of the most common cancers among women and the most lethal malignancy of all gynecological cancers. Surgery is promising in the early stages; however, most patients are first diagnosed in the advanced stages, where treatment options are limited. Here, we present a 49-year-old patient who was first diagnosed with stage III ovarian cancer. After the tumor progressed several times under guideline therapies with no more treatment options available at that time, the patient received a fully individualized neoantigen-derived peptide vaccine in the setting of an individual healing attempt. The tumor was analyzed for somatic mutations via whole exome sequencing and potential neoepitopes were vaccinated over a period of 50 months. During vaccination, the patient additionally received anti-PD-1 therapy to prevent further disease progression. Vaccine-induced T-cell responses were detected using intracellular cytokine staining. After eleven days of in vitro expansion, four T-cell activation markers (namely IFN-ɣ, TNF-α, IL-2, and CD154) were measured. The proliferation capacity of neoantigen-specific T-cells was determined using a CFSE proliferation assay. Immune monitoring revealed a very strong CD4+ T-cell response against one of the vaccinated peptides. The vaccine-induced T-cells simultaneously expressed CD154, TNF, IL-2, and IFN-ɣ and showed a strong proliferation capacity upon neoantigen stimulation. Next-generation sequencing, as well as immunohistochemical analysis, revealed a loss of Beta-2 microglobulin (B2M), which is essential for MHC class I presentation. The results presented here implicate that the application of neoantigen-derived peptide vaccines might be considered for those cancer stages, where promising therapeutic options are lacking. Furthermore, we provide more data that endorse the intensive investigation of B2M loss as a tumor escape mechanism in clinical trials using anti-cancer vaccines together with immune-checkpoint inhibitors.
卵巢癌是女性中最常见的癌症之一,也是所有妇科癌症中致死性最高的恶性肿瘤。手术在早期阶段很有前景;然而,大多数患者首次确诊时已处于晚期,此时治疗选择有限。在此,我们介绍一位49岁的患者,她首次被诊断为III期卵巢癌。在按照指南治疗肿瘤多次进展且当时已无更多治疗选择后,该患者在个体化的治疗尝试中接受了完全个体化的新抗原衍生肽疫苗。通过全外显子测序分析肿瘤的体细胞突变,并在50个月的时间里接种潜在的新表位。在接种疫苗期间,患者还接受了抗PD-1治疗以防止疾病进一步进展。使用细胞内细胞因子染色检测疫苗诱导的T细胞反应。在体外扩增11天后,检测四种T细胞激活标志物(即IFN-γ、TNF-α、IL-2和CD154)。使用CFSE增殖试验测定新抗原特异性T细胞的增殖能力。免疫监测显示针对其中一种接种肽的CD4+T细胞反应非常强烈。疫苗诱导的T细胞同时表达CD154、TNF、IL-2和IFN-γ,并在新抗原刺激下表现出很强的增殖能力。下一代测序以及免疫组化分析显示β2微球蛋白(B2M)缺失,而B2M对于MHC I类呈递至关重要。此处呈现的结果表明,对于缺乏有前景治疗选择的癌症阶段,可考虑应用新抗原衍生肽疫苗。此外,我们提供了更多数据,支持在使用抗癌疫苗联合免疫检查点抑制剂的临床试验中,深入研究B2M缺失作为一种肿瘤逃逸机制。