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ALPL-1 is a target for chimeric antigen receptor therapy in osteosarcoma

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dc.contributor.author Mensali, Nadia
dc.contributor.author Köksal, Hakan
dc.contributor.author Joaquina, Sandy
dc.contributor.author Wernhoff, Patrik
dc.contributor.author Casey, Nicholas P.
dc.contributor.author Romecin, Paola
dc.contributor.author Panisello, Carla
dc.contributor.author Rodriguez, René
dc.contributor.author Vimeux, Lene
dc.contributor.author Juzeniene, Asta
dc.contributor.author Myhre, Marit R.
dc.contributor.author Fåne, Anne
dc.contributor.author Ramírez, Carolina Castilla
dc.contributor.author Maggadottir, Solrun Melkorka
dc.contributor.author Duru, Adil Doganay
dc.contributor.author Georgoudaki, Anna Maria
dc.contributor.author Grad, Iwona
dc.contributor.author Maturana, Andrés Daniel
dc.contributor.author Gaudernack, Gustav
dc.contributor.author Kvalheim, Gunnar
dc.contributor.author Carcaboso, Angel M.
dc.contributor.author de Alava, Enrique
dc.contributor.author Donnadieu, Emmanuel
dc.contributor.author Bruland, Øyvind S.
dc.contributor.author Menendez, Pablo
dc.contributor.author Inderberg, Else Marit
dc.contributor.author Wälchli, Sébastien
dc.date.accessioned 2023-08-12T01:06:48Z
dc.date.available 2023-08-12T01:06:48Z
dc.date.issued 2023-06-08
dc.identifier.citation Mensali , N , Köksal , H , Joaquina , S , Wernhoff , P , Casey , N P , Romecin , P , Panisello , C , Rodriguez , R , Vimeux , L , Juzeniene , A , Myhre , M R , Fåne , A , Ramírez , C C , Maggadottir , S M , Duru , A D , Georgoudaki , A M , Grad , I , Maturana , A D , Gaudernack , G , Kvalheim , G , Carcaboso , A M , de Alava , E , Donnadieu , E , Bruland , Ø S , Menendez , P , Inderberg , E M & Wälchli , S 2023 , ' ALPL-1 is a target for chimeric antigen receptor therapy in osteosarcoma ' , Nature Communications , vol. 14 , no. 1 , 3375 , pp. 3375 . https://doi.org/10.1038/s41467-023-39097-x
dc.identifier.issn 2041-1723
dc.identifier.other 155771172
dc.identifier.other 7b786bae-f7a3-4819-96c7-71f819f1c9c5
dc.identifier.other 85161398175
dc.identifier.other 37291203
dc.identifier.other unpaywall: 10.1038/s41467-023-39097-x
dc.identifier.uri https://hdl.handle.net/20.500.11815/4388
dc.description Funding Information: The authors would like to thank our colleagues from the Translational Research Unit and the Flow cytometry Core facility of OUS for providing technical assistance. We are grateful to Gibco and Life Technologies AS for supplying CTS™ Dynabeads™ CD3/CD28 and Drs. Mengyu Wang and Hanne B. Scholz (Oslo University Hospital) for providing the mesenchymal stem cells. We thank Prof. Michael Nishimura (Loyola University Chicago Stritch School of Medicine, USA) for sharing the truncated CD34 sequence. This study was supported by the Norwegian Research Council (Grant numbers: 284983 and 316407 to S.W. and 326811 to E.M.I), the Norwegian Health Region South East (Grant numbers: 2020601, 2018579, 2016006 and 2019062 to S.W. and 2019004 to E.M.I.) and S.J. is supported by the Norwegian Research Council under the frame of the Era-Net EURONANOMED-3 European Research project “NAN-4-TUM”. We thank Nova Southeastern University Center for Collaborative Research Core Facilities personnel Dr. Robin Krueger, Solly-Ann Barton-Case and Dr. Bojie Dai for their support in generation of RNAseq data. A.-M.G. was supported by the Swedish Society for Medical Research (SSMF). Research in P.M.’s Laboratory was funded by “la Caixa” Foundation Validate Program, ISCIII-RICORS within the Next Generation EU program (plan de recuperación, transformación y resilencia), and core support from CERCA/Generalitat de Catalunya and Fundació Josep Carreras-Obra Social la Caixa, the CaixaImpulse Grant CI21-00189, which has received funding from the European Institute of Innovation and Technology (EIT). This body of the European Union receives support from the European Union’s Horizon 2021 research and innovation program. C.P. is supported by a PFIS fellowship from Instituto de Salud Carlos III (ISCIII) (FI21/00161). Figures 3 a, 3 e, 4a , ad Supplementary Fig. 4a were prepared using BioRender.com. Funding Information: The authors would like to thank our colleagues from the Translational Research Unit and the Flow cytometry Core facility of OUS for providing technical assistance. We are grateful to Gibco and Life Technologies AS for supplying CTS™ Dynabeads™ CD3/CD28 and Drs. Mengyu Wang and Hanne B. Scholz (Oslo University Hospital) for providing the mesenchymal stem cells. We thank Prof. Michael Nishimura (Loyola University Chicago Stritch School of Medicine, USA) for sharing the truncated CD34 sequence. This study was supported by the Norwegian Research Council (Grant numbers: 284983 and 316407 to S.W. and 326811 to E.M.I), the Norwegian Health Region South East (Grant numbers: 2020601, 2018579, 2016006 and 2019062 to S.W. and 2019004 to E.M.I.) and S.J. is supported by the Norwegian Research Council under the frame of the Era-Net EURONANOMED-3 European Research project “NAN-4-TUM”. We thank Nova Southeastern University Center for Collaborative Research Core Facilities personnel Dr. Robin Krueger, Solly-Ann Barton-Case and Dr. Bojie Dai for their support in generation of RNAseq data. A.-M.G. was supported by the Swedish Society for Medical Research (SSMF). Research in P.M.’s Laboratory was funded by “la Caixa” Foundation Validate Program, ISCIII-RICORS within the Next Generation EU program (plan de recuperación, transformación y resilencia), and core support from CERCA/Generalitat de Catalunya and Fundació Josep Carreras-Obra Social la Caixa, the CaixaImpulse Grant CI21-00189, which has received funding from the European Institute of Innovation and Technology (EIT). This body of the European Union receives support from the European Union’s Horizon 2021 research and innovation program. C.P. is supported by a PFIS fellowship from Instituto de Salud Carlos III (ISCIII) (FI21/00161). Figures a, e, , ad Supplementary Fig. were prepared using BioRender.com. Publisher Copyright: © 2023, The Author(s).
dc.description.abstract Osteosarcoma (OS) remains a dismal malignancy in children and young adults, with poor outcome for metastatic and recurrent disease. Immunotherapies in OS are not as promising as in some other cancer types due to intra-tumor heterogeneity and considerable off-target expression of the potentially targetable proteins. Here we show that chimeric antigen receptor (CAR) T cells could successfully target an isoform of alkaline phosphatase, ALPL-1, which is highly and specifically expressed in primary and metastatic OS. The target recognition element of the second-generation CAR construct is based on two antibodies, previously shown to react against OS. T cells transduced with these CAR constructs mediate efficient and effective cytotoxicity against ALPL-positive cells in in vitro settings and in state-of-the-art in vivo orthotopic models of primary and metastatic OS, without unexpected toxicities against hematopoietic stem cells or healthy tissues. In summary, CAR-T cells targeting ALPL-1 show efficiency and specificity in treating OS in preclinical models, paving the path for clinical translation.
dc.format.extent 2830905
dc.format.extent 3375
dc.language.iso en
dc.relation.ispartofseries Nature Communications; 14(1)
dc.rights info:eu-repo/semantics/openAccess
dc.subject Child
dc.subject Humans
dc.subject Immunotherapy, Adoptive
dc.subject T-Lymphocytes
dc.subject Immunotherapy
dc.subject Osteosarcoma/therapy
dc.subject Bone Neoplasms/therapy
dc.subject Cell Line, Tumor
dc.subject Alkaline Phosphatase
dc.subject General Physics and Astronomy
dc.subject General Chemistry
dc.subject General Biochemistry,Genetics and Molecular Biology
dc.title ALPL-1 is a target for chimeric antigen receptor therapy in osteosarcoma
dc.type /dk/atira/pure/researchoutput/researchoutputtypes/contributiontojournal/article
dc.description.version Peer reviewed
dc.identifier.doi 10.1038/s41467-023-39097-x
dc.relation.url http://www.scopus.com/inward/record.url?scp=85161398175&partnerID=8YFLogxK
dc.contributor.department Faculty of Medicine


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