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Time 2EVOLVE: predicting efficacy of engineered T-cells - how far is the bench from the bedside?
Guedan, Sonia; Luu, Maik; Ammar, Delphine; Barbao, Paula; Bonini, Chiara; Bousso, Philippe; Buchholz, Christian J; Casucci, Monica; De Angelis, Biagio; Donnadieu, Emmanuel; Espie, David; Greco, Beatrice; Groen, Richard; Huppa, Johannes B; Kantari-Mimoun, Chahrazade; Laugel, Bruno; Mantock, Mary; Markman, Janet L; Morris, Emma; Quintarelli, Concetta; Rade, Michael; Reiche, Kristin; Rodriguez-Garcia, Alba; Rodriguez-Madoz, Juan Roberto; Ruggiero, Eliana; Themeli, Maria; Hudecek, Michael; Marchiq, Ibtissam.
Afiliação
  • Guedan S; Department of Hematology and Oncology, Hospital Clinic, IDIBAPS, Barcelona, Spain sguedan@clinic.cat ibtissam.marchiq@servier.com.
  • Luu M; 19 Lehrstuhl für Zelluläre Immuntherapie, Medizinische Klinik und Poliklinik II, Universitätsklinikum Würzburg, Wurzburg, Germany.
  • Ammar D; Astellas Pharma Inc, Leiden, The Netherlands.
  • Barbao P; Department of Hematology and Oncology, Hospital Clinic, IDIBAPS, Barcelona, Spain.
  • Bonini C; Experimental Hematology Unit, IRCCS San Raffaele Scientific Institute, Milano, Italy.
  • Bousso P; Institut Pasteur, Université de Paris Cité, Inserm U1223, Paris, France.
  • Buchholz CJ; Paul-Ehrlich-Institut, Langen, Germany.
  • Casucci M; Innovative Immunotherapies Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
  • De Angelis B; Department Onco-Haematology, and Cell and Gene Therapy, Bambino Gesù Children Hospital, IRCCS, Rome, Italy.
  • Donnadieu E; Université Paris Cité, CNRS, INSERM, Equipe Labellisée Ligue Contre le Cancer, Institut Cochin, F-75014 Paris, France.
  • Espie D; Université Paris Cité, CNRS, INSERM, Equipe Labellisée Ligue Contre le Cancer, Institut Cochin, F-75014 Paris, France.
  • Greco B; CAR-T Cells Department, Invectys, Paris, France.
  • Groen R; Innovative Immunotherapies Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
  • Huppa JB; Amsterdam University Medical Centers at Vrije Universiteit, Cancer Center Amsterdam, Amsterdam, The Netherlands.
  • Kantari-Mimoun C; Medical University of Vienna, Center for Pathophysiology, Infectiology and Immunology, Institute for Hygiene and Applied Immunolgy, Vienna, Austria.
  • Laugel B; Institut de Recherches internationales Servier (IRIS), Suresnes, France.
  • Mantock M; Institut de Recherches internationales Servier (IRIS), Suresnes, France.
  • Markman JL; Astellas Pharma Inc, Leiden, The Netherlands.
  • Morris E; Takeda Development Centers Americas, Inc. Lexington, Massachusetts, USA.
  • Quintarelli C; Institute of Immunity & Transplantation, University College London Medical School - Royal Free Campus, London, UK.
  • Rade M; Department Onco-Haematology, and Cell and Gene Therapy, Bambino Gesù Children Hospital, IRCCS, Rome, Italy.
  • Reiche K; Fraunhofer Institute for Cell Therapy and Immunology IZI, Leipzig, Germany.
  • Rodriguez-Garcia A; Fraunhofer Institute for Cell Therapy and Immunology IZI, Leipzig, Germany.
  • Rodriguez-Madoz JR; Department of Hematology and Oncology, Hospital Clinic, IDIBAPS, Barcelona, Spain.
  • Ruggiero E; Hemato-Oncology Program, CIMA Universidad de Navarra, Pamplona, Spain.
  • Themeli M; Experimental Hematology Unit, IRCCS San Raffaele Scientific Institute, Milano, Italy.
  • Hudecek M; Amsterdam University Medical Centers at Vrije Universiteit, Cancer Center Amsterdam, Amsterdam, The Netherlands.
  • Marchiq I; 19 Lehrstuhl für Zelluläre Immuntherapie, Medizinische Klinik und Poliklinik II, Universitätsklinikum Würzburg, Wurzburg, Germany.
J Immunother Cancer ; 10(5)2022 05.
Article em En | MEDLINE | ID: mdl-35577501
ABSTRACT
Immunotherapy with gene engineered CAR and TCR transgenic T-cells is a transformative treatment in cancer medicine. There is a rich pipeline with target antigens and sophisticated technologies that will enable establishing this novel treatment not only in rare hematological malignancies, but also in common solid tumors. The T2EVOLVE consortium is a public private partnership directed at accelerating the preclinical development of and increasing access to engineered T-cell immunotherapies for cancer patients. A key ambition in T2EVOLVE is to assess the currently available preclinical models for evaluating safety and efficacy of engineered T cell therapy and developing new models and test parameters with higher predictive value for clinical safety and efficacy in order to improve and accelerate the selection of lead T-cell products for clinical translation. Here, we review existing and emerging preclinical models that permit assessing CAR and TCR signaling and antigen binding, the access and function of engineered T-cells to primary and metastatic tumor ligands, as well as the impact of endogenous factors such as the host immune system and microbiome. Collectively, this review article presents a perspective on an accelerated translational development path that is based on innovative standardized preclinical test systems for CAR and TCR transgenic T-cell products.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Receptores de Antígenos Quiméricos / Neoplasias Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: J Immunother Cancer Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Receptores de Antígenos Quiméricos / Neoplasias Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: J Immunother Cancer Ano de publicação: 2022 Tipo de documento: Article