Trial watch: anticancer vaccination with dendritic cells

Bibliographic Details
Title: Trial watch: anticancer vaccination with dendritic cells
Authors: Francisca Borges, Raquel S. Laureano, Isaure Vanmeerbeek, Jenny Sprooten, Octavie Demeulenaere, Jannes Govaerts, Lisa Kinget, Saurabh Saraswat, Benoit Beuselinck, Steven De Vleeschouwer, Paul Clement, Frederik De Smet, RĂ¼diger V. Sorg, Angeliki Datsi, Nathalie Vigneron, Stefan Naulaerts, Abhishek D. Garg
Source: OncoImmunology, Vol 13, Iss 1 (2024)
Publisher Information: Taylor & Francis Group, 2024.
Publication Year: 2024
Collection: LCC:Immunologic diseases. Allergy
LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
Subject Terms: Antigen cross-presentation, clinical trial, DAMPs, dendritic cells, immune checkpoint blockers, T cell priming, Immunologic diseases. Allergy, RC581-607, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
More Details: Dendritic cells (DCs) are critical players at the intersection of innate and adaptive immunity, making them ideal candidates for anticancer vaccine development. DC-based immunotherapies typically involve isolating patient-derived DCs, pulsing them with tumor-associated antigens (TAAs) or tumor-specific antigens (TSAs), and utilizing maturation cocktails to ensure their effective activation. These matured DCs are then reinfused to elicit tumor-specific T-cell responses. While this approach has demonstrated the ability to generate potent immune responses, its clinical efficacy has been limited due to the immunosuppressive tumor microenvironment. Recent efforts have focused on enhancing the immunogenicity of DC-based vaccines, particularly through combination therapies with T cell-targeting immunotherapies. This Trial Watch summarizes recent advances in DC-based cancer treatments, including the development of new preclinical and clinical strategies, and discusses the future potential of DC-based vaccines in the evolving landscape of immuno-oncology.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2162402X
2162-402X
Relation: https://doaj.org/toc/2162-402X
DOI: 10.1080/2162402X.2024.2412876
Access URL: https://doaj.org/article/62ea562a7fa84a7596a062de5d9f27c9
Accession Number: edsdoj.62ea562a7fa84a7596a062de5d9f27c9
Database: Directory of Open Access Journals
More Details
ISSN:2162402X
DOI:10.1080/2162402X.2024.2412876
Published in:OncoImmunology
Language:English