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Small-scale manufacturing of neoantigen-encoding messenger RNA for early-phase clinical trials.
Ingels, Joline; De Cock, Laurenz; Mayer, Rupert L; Devreker, Pam; Weening, Karin; Heyns, Kelly; Lootens, Nele; De Smet, Saskia; Brusseel, Marieke; De Munter, Stijn; Pille, Melissa; Billiet, Lore; Goetgeluk, Glenn; Bonte, Sarah; Jansen, Hanne; Lint, Sandra Van; Leclercq, Georges; Taghon, Tom; Menten, Björn; Vermaelen, Karim; Impens, Francis; Vandekerckhove, Bart.
Afiliação
  • Ingels J; Department of Diagnostic Sciences, Ghent University, Ghent, Belgium; Cancer Research Institute, Ghent, Belgium.
  • De Cock L; Cancer Research Institute, Ghent, Belgium; Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
  • Mayer RL; Department of Biomolecular Medicine, Ghent University, Ghent, Belgium; VIB-UGent Center for Medical Biotechnology, Vlaams Instituut voor Biotechnologie, Ghent, Belgium.
  • Devreker P; Cell Therapy Unit, Department of Regenerative Medicine, Ghent University Hospital, Ghent, Belgium.
  • Weening K; Department of Diagnostic Sciences, Ghent University, Ghent, Belgium.
  • Heyns K; Department of Respiratory Medicine, Ghent University Hospital, Ghent, Belgium.
  • Lootens N; Cell Therapy Unit, Department of Regenerative Medicine, Ghent University Hospital, Ghent, Belgium.
  • De Smet S; Cell Therapy Unit, Department of Regenerative Medicine, Ghent University Hospital, Ghent, Belgium.
  • Brusseel M; Cell Therapy Unit, Department of Regenerative Medicine, Ghent University Hospital, Ghent, Belgium.
  • De Munter S; Department of Diagnostic Sciences, Ghent University, Ghent, Belgium; Cancer Research Institute, Ghent, Belgium.
  • Pille M; Department of Diagnostic Sciences, Ghent University, Ghent, Belgium.
  • Billiet L; Department of Diagnostic Sciences, Ghent University, Ghent, Belgium.
  • Goetgeluk G; Department of Diagnostic Sciences, Ghent University, Ghent, Belgium; Cancer Research Institute, Ghent, Belgium.
  • Bonte S; Cancer Research Institute, Ghent, Belgium; Department of Internal Medicine and Pediatrics, Ghent University, Ghent, Belgium.
  • Jansen H; Department of Diagnostic Sciences, Ghent University, Ghent, Belgium.
  • Lint SV; Cancer Research Institute, Ghent, Belgium; Department of Respiratory Medicine, Ghent University Hospital, Ghent, Belgium.
  • Leclercq G; Department of Diagnostic Sciences, Ghent University, Ghent, Belgium.
  • Taghon T; Department of Diagnostic Sciences, Ghent University, Ghent, Belgium.
  • Menten B; Cancer Research Institute, Ghent, Belgium; Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
  • Vermaelen K; Cancer Research Institute, Ghent, Belgium; Department of Respiratory Medicine, Ghent University Hospital, Ghent, Belgium.
  • Impens F; Cancer Research Institute, Ghent, Belgium; Department of Biomolecular Medicine, Ghent University, Ghent, Belgium; VIB-UGent Center for Medical Biotechnology, Vlaams Instituut voor Biotechnologie, Ghent, Belgium.
  • Vandekerckhove B; Department of Diagnostic Sciences, Ghent University, Ghent, Belgium; Cancer Research Institute, Ghent, Belgium; Cell Therapy Unit, Department of Regenerative Medicine, Ghent University Hospital, Ghent, Belgium. Electronic address: bart.vandekerckhove@ugent.be.
Cytotherapy ; 24(2): 213-222, 2022 02.
Article em En | MEDLINE | ID: mdl-34696961
ABSTRACT
Messenger RNA (mRNA) has become a promising tool in therapeutic cancer vaccine strategies. Owing to its flexible design and rapid production, mRNA is an attractive antigen delivery format for cancer vaccines targeting mutated peptides expressed in a tumor-the so-called neoantigens. These neoantigens are rarely shared between patients, and inclusion of these antigens in a vaccine requires the production of individual batches of patient-tailored mRNA. The authors have developed MIDRIXNEO, a personalized mRNA-loaded dendritic cell vaccine targeting tumor neoantigens, which is currently being evaluated in a phase 1 clinical study in lung cancer patients. To facilitate this study, the authors set up a Good Manufacturing Practice (GMP)-compliant production process for the manufacture of small batches of personalized neoantigen-encoding mRNA. In this article, the authors describe the complete mRNA production process and the extensive quality assessment to which the mRNA is subjected. Validation runs have shown that the process delivers mRNA of reproducible, high quality. This process is now successfully applied for the production of neoantigen-encoding mRNA for the clinical evaluation of MIDRIXNEO. To the authors' knowledge, this is the first time that a GMP-based production process of patient-tailored neoantigen mRNA has been described.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas Anticâncer / Neoplasias Pulmonares / Neoplasias Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas Anticâncer / Neoplasias Pulmonares / Neoplasias Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article