Daradoumis Joana, Müller Mikkel Dons, Neckermann Patrick, Asbach Benedikt, Schrödel Silke, Thirion Christian, Wagner Ralf, Thor Straten Per, Holst Peter Johannes, Boilesen Ditte
InProTher ApS, Bioinnovation Institute, Ole Maaløes Vej 3, 2200 Copenhagen, Denmark.
Department of Immunology and Microbiology, University of Copenhagen, Blegdamsvej 3B, 2200 Copenhagen, Denmark.
Cancers (Basel). 2023 Dec 15;15(24):5863. doi: 10.3390/cancers15245863.
Persistent human papillomavirus (HPV) infection is responsible for practically all cervical and a high proportion of anogenital and oropharyngeal cancers. Therapeutic HPV vaccines in clinical development show great promise in improving outcomes for patients who mount an anti-HPV T-cell response; however, far from all patients elicit a sufficient immunological response. This demonstrates a translational gap between animal models and human patients. Here, we investigated the potential of a new assay consisting of co-culturing vaccine-transduced dendritic cells (DCs) with syngeneic, healthy, human peripheral blood mononuclear cells (PBMCs) to mimic a human in vivo immunization. This new promising human ex vivo PBMC assay was evaluated using an innovative therapeutic adenovirus (Adv)-based HPV vaccine encoding the E1, E2, E6, and E7 HPV16 genes. This new method allowed us to show that vaccine-transduced DCs yielded functional effector T cells and unveiled information on immunohierarchy, showing E1-specific T-cell immunodominance over time. We suggest that this assay can be a valuable translational tool to complement the known animal models, not only for HPV therapeutic vaccines, and supports the use of E1 as an immunotherapeutic target. Nevertheless, the findings reported here need to be validated in a larger number of donors and preferably in patient samples.
持续性人乳头瘤病毒(HPV)感染几乎是所有宫颈癌以及很大一部分肛门生殖器癌和口咽癌的病因。处于临床开发阶段的治疗性HPV疫苗在改善能够产生抗HPV T细胞应答的患者的治疗效果方面显示出巨大潜力;然而,远非所有患者都能引发足够的免疫应答。这表明动物模型与人类患者之间存在转化差距。在此,我们研究了一种新检测方法的潜力,该方法是将经疫苗转导的树突状细胞(DC)与同基因的健康人外周血单核细胞(PBMC)共培养,以模拟人体的体内免疫接种。我们使用一种基于创新治疗性腺病毒(Adv)的HPV疫苗对这种新的、有前景的人离体PBMC检测方法进行了评估,该疫苗编码HPV16的E1、E2、E6和E7基因。这种新方法使我们能够证明经疫苗转导的DC产生了功能性效应T细胞,并揭示了免疫层次结构方面的信息,显示随着时间推移E1特异性T细胞具有免疫优势。我们认为,这种检测方法可以成为一种有价值的转化工具,以补充已知的动物模型,不仅适用于HPV治疗性疫苗,还支持将E1用作免疫治疗靶点。尽管如此,此处报告的研究结果需要在更多的供体中进行验证,最好是在患者样本中进行验证。