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Trial watch: Dendritic cell (DC)-based immunotherapy for cancer.
Laureano, Raquel S; Sprooten, Jenny; Vanmeerbeerk, Isaure; Borras, Daniel M; Govaerts, Jannes; Naulaerts, Stefan; Berneman, Zwi N; Beuselinck, Benoit; Bol, Kalijn F; Borst, Jannie; Coosemans, An; Datsi, Angeliki; Fucíková, Jitka; Kinget, Lisa; Neyns, Bart; Schreibelt, Gerty; Smits, Evelien; Sorg, Rüdiger V; Spisek, Radek; Thielemans, Kris; Tuyaerts, Sandra; De Vleeschouwer, Steven; de Vries, I Jolanda M; Xiao, Yanling; Garg, Abhishek D.
Affiliation
  • Laureano RS; Laboratory of Cell Stress & Immunity, Department of Cellular & Molecular Medicine, KU Leuven, Leuven, Belgium.
  • Sprooten J; Laboratory of Cell Stress & Immunity, Department of Cellular & Molecular Medicine, KU Leuven, Leuven, Belgium.
  • Vanmeerbeerk I; Laboratory of Cell Stress & Immunity, Department of Cellular & Molecular Medicine, KU Leuven, Leuven, Belgium.
  • Borras DM; Laboratory of Cell Stress & Immunity, Department of Cellular & Molecular Medicine, KU Leuven, Leuven, Belgium.
  • Govaerts J; Laboratory of Cell Stress & Immunity, Department of Cellular & Molecular Medicine, KU Leuven, Leuven, Belgium.
  • Naulaerts S; Laboratory of Cell Stress & Immunity, Department of Cellular & Molecular Medicine, KU Leuven, Leuven, Belgium.
  • Berneman ZN; Department of Haematology, Antwerp University Hospital, Edegem, Belgium.
  • Beuselinck B; Vaccine and Infectious Disease Institute, Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.
  • Bol KF; Center for Cell Therapy and Regenerative Medicine, Antwerp University Hospital, Edegem, Belgium.
  • Borst J; Department of General Medical Oncology, UZ Leuven, Leuven, Belgium.
  • Coosemans A; Department of Tumour Immunology, Radboud Institute for Molecular Life Sciences; Radboud University Medical Center, Nijmegen, The Netherlands.
  • Datsi A; Department of Medical Oncology, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Fucíková J; Department of Immunology and Oncode Institute, Leiden University Medical Center, Leiden, The Netherlands.
  • Kinget L; Department of Oncology, Laboratory of Tumor Immunology and Immunotherapy, ImmunOvar Research Group, Ku Leuven, Leuven Cancer Institute, Leuven, Belgium.
  • Neyns B; Institute for Transplantation Diagnostics and Cell Therapeutics, Heinrich-Heine University, Düsseldorf, Germany.
  • Schreibelt G; Sotio Biotech, Prague, Czech Republic.
  • Smits E; Department of Immunology, Charles University, University Hospital Motol, Prague, Czech Republic.
  • Sorg RV; Department of General Medical Oncology, UZ Leuven, Leuven, Belgium.
  • Spisek R; Department of Medical Oncology, UZ Brussel, Brussels, Belgium.
  • Thielemans K; Department of Tumour Immunology, Radboud Institute for Molecular Life Sciences; Radboud University Medical Center, Nijmegen, The Netherlands.
  • Tuyaerts S; Center for Cell Therapy and Regenerative Medicine, Antwerp University Hospital, Edegem, Belgium.
  • De Vleeschouwer S; Center for Oncological Research, Integrated Personalized and Precision Oncology Network, University of Antwerp, Wilrijk, Belgium.
  • de Vries IJM; Institute for Transplantation Diagnostics and Cell Therapeutics, Heinrich-Heine University, Düsseldorf, Germany.
  • Xiao Y; Sotio Biotech, Prague, Czech Republic.
  • Garg AD; Department of Immunology, Charles University, University Hospital Motol, Prague, Czech Republic.
Oncoimmunology ; 11(1): 2096363, 2022.
Article in En | MEDLINE | ID: mdl-35800158
Dendritic cell (DC)-based vaccination for cancer treatment has seen considerable development over recent decades. However, this field is currently in a state of flux toward niche-applications, owing to recent paradigm-shifts in immuno-oncology mobilized by T cell-targeting immunotherapies. DC vaccines are typically generated using autologous (patient-derived) DCs exposed to tumor-associated or -specific antigens (TAAs or TSAs), in the presence of immunostimulatory molecules to induce DC maturation, followed by reinfusion into patients. Accordingly, DC vaccines can induce TAA/TSA-specific CD8+/CD4+ T cell responses. Yet, DC vaccination still shows suboptimal anti-tumor efficacy in the clinic. Extensive efforts are ongoing to improve the immunogenicity and efficacy of DC vaccines, often by employing combinatorial chemo-immunotherapy regimens. In this Trial Watch, we summarize the recent preclinical and clinical developments in this field and discuss the ongoing trends and future perspectives of DC-based immunotherapy for oncological indications.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cancer Vaccines / Neoplasms Limits: Humans Language: En Journal: Oncoimmunology Year: 2022 Document type: Article Affiliation country: Bélgica Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cancer Vaccines / Neoplasms Limits: Humans Language: En Journal: Oncoimmunology Year: 2022 Document type: Article Affiliation country: Bélgica Country of publication: Estados Unidos