Autologous anti-GD2 CAR T cells efficiently target primary human glioblastoma

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作者
Chiara Chiavelli
Malvina Prapa
Giulia Rovesti
Marco Silingardi
Giovanni Neri
Giuseppe Pugliese
Lucia Trudu
Massimiliano Dall’Ora
Giulia Golinelli
Giulia Grisendi
Jonathan Vinet
Marco Bestagno
Carlotta Spano
Roberto Vito Papapietro
Roberta Depenni
Katia Di Emidio
Anna Pasetto
Daniela Nascimento Silva
Alberto Feletti
Silvia Berlucchi
Corrado Iaccarino
Giacomo Pavesi
Massimo Dominici
机构
[1] University of Modena and Reggio Emilia,Laboratory of Cellular Therapy, Division of Oncology, Department of Medical and Surgical Sciences for Children & Adults
[2] University of Modena and Reggio Emilia,Clinical and Experimental Medicine PhD Program
[3] University-Hospital of Modena and Reggio Emilia,Department of Oncology and Hematology
[4] Great Maze Pond,Leucid Bio Ltd., Guy’s Hospital
[5] Evotec (Modena) Srl,Center for Cellular Immunotherapies
[6] Medolla,Centro Interdipartimentale Grandi Strumenti (CIGS)
[7] Perelman School of Medicine,Department of Biomedical, Metabolic and Neural Sciences
[8] and Parker Institute for Cancer Immunotherapy at University of Pennsylvania,Section for Cell Therapy, Radiumhospitalet
[9] University of Modena and Reggio Emilia,Department of Laboratory Medicine
[10] International Centre for Genetic Engineering and Biotechnology,Department of Neurosciences, Biomedicine and Movement Sciences, Neurosurgery Unit
[11] University of Modena and Reggio Emilia,Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia
[12] Oslo University Hospital, Division of Neurosurgery, Department of Neurosciences
[13] Karolinska Institutet,undefined
[14] University of Verona,undefined
[15] University-Hospital of Modena and Reggio Emilia,undefined
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摘要
Glioblastoma (GBM) remains a deadly tumor. Treatment with chemo-radiotherapy and corticosteroids is known to impair the functionality of lymphocytes, potentially compromising the development of autologous CAR T cell therapies. We here generated pre-clinical investigations of autologous anti-GD2 CAR T cells tested against 2D and 3D models of GBM primary cells. We detected a robust antitumor effect, highlighting the feasibility of developing an autologous anti-GD2 CAR T cell-based therapy for GBM patients.
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