Heitmann Jonas S, Jung Susanne, Wacker Marcel, Maringer Yacine, Nelde Annika, Bauer Jens, Denk Monika, Hoenisch-Gravel Naomi, Richter Marion, Oezbek Melek T, Dubbelaar Marissa L, Bilich Tatjana, Pumptow Marina, Martus Peter, Illerhaus Gerald, Denzlinger Claudio, Steinbach Francesca, Aulitzky Walter-Erich, Müller Martin R, Dörfel Daniela, Rammensee Hans-Georg, Salih Helmut R, Walz Juliane S
Clinical Collaboration Unit Translational Immunology, German Cancer Consortium (DKTK), Department of Internal Medicine, University Hospital Tübingen, Tübingen, Germany.
Cluster of Excellence iFIT (EXC2180) "Image-Guided and Functionally Instructed Tumor Therapies", University of Tübingen, Tübingen, Germany.
Front Immunol. 2024 Nov 26;15:1482715. doi: 10.3389/fimmu.2024.1482715. eCollection 2024.
Cancer peptide vaccination represents a promising therapeutic approach, but has been hampered by lack of suitable antigens and restricted applicability due to different HLA backgrounds of individual patients. We here introduce a novel warehouse-based concept for composition of personalized peptide vaccines and report on its successful application in a Phase II clinical trial in patients with chronic lymphocytic leukemia (CLL) after first-line therapy. 26 CLL patients in at least partial remission (PR) after 6 months of immuno-chemotherapy were vaccinated with a personalized vaccine compiled from a premanufactured peptide warehouse comprising immunopeptidome-defined CLL-associated peptides. Primary objective was evaluation of immunogenicity, secondary objectives were safety and minimal residual disease (MRD) response. Immunopeptidome-guided vaccine composition was throughout successful, proving the feasibility of warehouse-based vaccine design. Vaccination was well tolerated, with local injection site reactions being the most common adverse event. Only few patients showed vaccine-induced T cell responses, attributable to their inability to mount strong immune responses due to immune-chemotherapy and lack of potent adjuvant formulations. Both issues are addressed within a follow-up trial (NCT04688385), combining the immunopeptidome-guided warehouse-based vaccine design reported here with a potent novel adjuvant evaluating personalized multi- peptide vaccination in CLL patients under T cell supportive BTK inhibitor therapies.
www.clinicaltrialsregister.eu, identifier NCT02802943.
癌症肽疫苗接种是一种有前景的治疗方法,但由于缺乏合适的抗原以及个体患者不同的HLA背景导致适用性受限,其发展受到阻碍。我们在此引入一种基于仓库的个性化肽疫苗组成新概念,并报告其在一线治疗后的慢性淋巴细胞白血病(CLL)患者的II期临床试验中的成功应用。26例在免疫化疗6个月后至少达到部分缓解(PR)的CLL患者接种了由包含免疫肽组定义的CLL相关肽的预制肽库编制而成的个性化疫苗。主要目标是评估免疫原性,次要目标是安全性和微小残留病(MRD)反应。免疫肽组引导的疫苗组成始终成功,证明了基于仓库的疫苗设计的可行性。疫苗接种耐受性良好,局部注射部位反应是最常见的不良事件。只有少数患者表现出疫苗诱导的T细胞反应,这归因于他们由于免疫化疗而无法产生强烈的免疫反应以及缺乏有效的佐剂配方。在一项后续试验(NCT04688385)中解决了这两个问题,该试验将本文报道的免疫肽组引导的基于仓库的疫苗设计与一种有效的新型佐剂相结合,在T细胞支持性BTK抑制剂治疗下评估CLL患者的个性化多肽疫苗接种。