Related Experiment Video
Updated: Sep 29, 2025

Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
A novel immunopeptidomic-based pipeline for the generation of personalized oncolytic cancer vaccines
Sara Feola1,2,3, Jacopo Chiaro1,2,3, Beatriz Martins1,2,3
1Drug Research Program (DRP) ImmunoViroTherapy Lab (IVT), Division of Pharmaceutical Biosciences, Faculty of Pharmacy, Viikinkaari 5E, University of Helsinki, Helsinki, Finland.
Abstract:
Besides the isolation and identification of major histocompatibility complex I-restricted peptides from the surface of cancer cells, one of the challenges is eliciting an effective antitumor CD8+ T-cell-mediated response as part of therapeutic cancer vaccine. Therefore, the establishment of a solid pipeline for the downstream selection of clinically relevant peptides and the subsequent creation of therapeutic cancer vaccines are of utmost importance. Indeed, the use of peptides for eliciting specific antitumor adaptive immunity is hindered by two main limitations: the efficient selection of the most optimal candidate peptides and the use of a highly immunogenic platform to combine with the peptides to induce effective tumor-specific adaptive immune responses. Here, we describe for the first time a streamlined pipeline for the generation of personalized cancer vaccines starting from the isolation and selection of the most immunogenic peptide candidates expressed on the tumor cells and ending in the generation of efficient therapeutic oncolytic cancer vaccines. This immunopeptidomics-based pipeline was carefully validated in a murine colon tumor model CT26. Specifically, we used state-of-the-art immunoprecipitation and mass spectrometric methodologies to isolate >8000 peptide targets from the CT26 tumor cell line. The selection of the target candidates was then based on two separate approaches: RNAseq analysis and HEX software. The latter is a tool previously developed by Jacopo, 2020, able to identify tumor antigens similar to pathogen antigens in order to exploit molecular mimicry and tumor pathogen cross-reactive T cells in cancer vaccine development. The generated list of candidates (26 in total) was further tested in a functional characterization assay using interferon-γ enzyme-linked immunospot (ELISpot), reducing the number of candidates to six. These peptides were then tested in our previously described oncolytic cancer vaccine platform PeptiCRAd, a vaccine platform that combines an immunogenic oncolytic adenovirus (OAd) coated with tumor antigen peptides. In our work, PeptiCRAd was successfully used for the treatment of mice bearing CT26, controlling the primary malignant lesion and most importantly a secondary, nontreated, cancer lesion. These results confirmed the feasibility of applying the described pipeline for the selection of peptide candidates and generation of therapeutic oncolytic cancer vaccine, filling a gap in the field of cancer immunotherapy, and paving the way to translate our pipeline into human therapeutic approach.
Insights
We developed a streamlined pipeline to create personalized cancer vaccines by identifying tumor-specific peptides and using an oncolytic adenovirus platform. This approach successfully controlled tumor growth in mice, offering a promising new avenue for cancer immunotherapy.
Area of Science:
- Immunology
- Oncology
- Vaccine Development
Background:
- Eliciting effective antitumor CD8+ T-cell responses for cancer vaccines is challenging.
- Selecting optimal peptide candidates and using immunogenic platforms are key limitations in peptide-based cancer vaccines.
Purpose of the Study:
- To establish a streamlined, immunopeptidomics-based pipeline for generating personalized cancer vaccines.
- To validate the pipeline using a murine colon tumor model (CT26) and an oncolytic cancer vaccine platform (PeptiCRAd).
Main Methods:
- Isolation of >8000 peptides from CT26 tumor cells using immunoprecipitation and mass spectrometry.
- Selection of peptide candidates via RNAseq analysis and HEX software, followed by functional validation using interferon-γ ELISpot assays.
- Testing selected peptides with the PeptiCRAd oncolytic cancer vaccine platform in a CT26 murine model.
Main Results:
- Identified and selected immunogenic peptides from CT26 tumor cells.
- The PeptiCRAd vaccine platform, incorporating selected peptides, demonstrated significant control of primary and secondary tumors in mice.
- Validated the pipeline's feasibility for generating effective therapeutic oncolytic cancer vaccines.
Conclusions:
- The developed pipeline offers a robust method for selecting personalized cancer vaccine candidates.
- The PeptiCRAd platform combined with selected peptides shows therapeutic potential in controlling cancer progression.
- This approach represents a significant advancement in cancer immunotherapy, with potential for human therapeutic translation.
More Related Videos
07:33Preparation, Characteristics, Toxicity, and Efficacy Evaluation of the Nasal Self-Assembled Nanoemulsion Tumor Vaccine In Vitro and In Vivo
Published on: September 28, 2022
10:18Author Spotlight: Magnetic Fluorescent Bead-Based Dual-Reporter Flow Analysis of PDL1-Vaxx Peptide Vaccine-Induced Antibody Blockade of the PD-1/PD-L1 Interaction
Published on: July 7, 2023
Related Concept Videos
Tumor Immunotherapy
Cancer Vaccines
Cancer vaccines come in two categories: preventive (prophylactic) and treatment (active). Preventive vaccines, such as the Human Papillomavirus (HPV) vaccine, protect against viruses that cause certain...
Combination Therapies and Personalized Medicine
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...
Targeted Cancer Therapies
There are several types of targeted therapies against...