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dc.contributor.authorMensali, Nadiaes_ES
dc.contributor.authorKöksal, Hakanes_ES
dc.contributor.authorJoaquina, Sandyes_ES
dc.contributor.authorWernhoff, Patrikes_ES
dc.contributor.authorCasey, Nicholas P.es_ES
dc.contributor.authorRomecin, Paolaes_ES
dc.contributor.authorPanisello, Carlaes_ES
dc.contributor.authorRodriguez, Renées_ES
dc.contributor.authorVimeux, Lenees_ES
dc.contributor.authorJuzeniene, Astaes_ES
dc.contributor.authorMyhre, Marit R.es_ES
dc.contributor.authorFåne, Annees_ES
dc.contributor.authorCastilla, Carolinaes_ES
dc.contributor.authorMaggadottir, Solrun Melkorkaes_ES
dc.contributor.authorDuru, Adil Doganayes_ES
dc.contributor.authorGeorgoudaki, Anna-Mariaes_ES
dc.contributor.authorGrad, Iwonaes_ES
dc.contributor.authorMaturana, Andrés Danieles_ES
dc.contributor.authorGaudernack, Gustaves_ES
dc.contributor.authorKvalheim, Gunnares_ES
dc.contributor.authorCarcaboso, Ángel M.es_ES
dc.contributor.authorÁlava, Enrique dees_ES
dc.contributor.authorDonnadieu, Emmanueles_ES
dc.contributor.authorBruland, Øyvind S.es_ES
dc.contributor.authorMenéndez, Pabloes_ES
dc.contributor.authorInderberg, Else Marites_ES
dc.contributor.authorWälchli, Sébastienes_ES
dc.date.accessioned2023-10-23T07:18:28Z-
dc.date.available2023-10-23T07:18:28Z-
dc.date.issued2023-06-08-
dc.identifier.citationNature Communications 14: 3375 (2023)es_ES
dc.identifier.urihttp://hdl.handle.net/10261/337533-
dc.description.abstractOsteosarcoma (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.es_ES
dc.description.sponsorshipThis 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).es_ES
dc.formatapplication/pdfes_ES
dc.language.isoenges_ES
dc.publisherSpringer Naturees_ES
dc.relation.isversionofPublisher's versiones_ES
dc.relation.isbasedonMensali, Nadia; Köksal, Hakan; Joaquina, Sandy; Wernhoff, Patrik; Casey, Nicholas P.; Romecin, Paola; Panisello, Carla; Rodriguez, René; Vimeux, Lene; Juzeniene, Asta; Myhre, Marit R.; Fåne, Anne; Castilla, Carolina; Maggadottir, Solrun Melkorka; Duru, Adil Doganay; Georgoudaki, Anna-Maria; Grad, Iwona; Maturana, Andrés Daniel; Gaudernack, Gustav; Kvalheim, Gunnar; Carcaboso, Ángel M.; Álava, Enrique de; Donnadieu, Emmanuel; Bruland, Øyvind S.; Menéndez, Pablo; Inderberg, Else Marit; Wälchli, Sébastien; 2023; Supplementary information. ALPL-1 is a target for chimeric antigen receptor therapy in osteosarcoma [Dataset]; Springer Nature; https://doi.org/10.1038/s41467-023-39097-xes_ES
dc.relation.isbasedonThe underlying dataset has been published as supplementary material of the article in the publisher platform at https://doi.org/10.1038/s41467-023-39097-xes_ES
dc.rightsopenAccesses_ES
dc.titleALPL-1 is a target for chimeric antigen receptor therapy in osteosarcomaes_ES
dc.typeartículoes_ES
dc.identifier.doi10.1038/s41467-023-39097-x-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.1038/s41467-023-39097-xes_ES
dc.identifier.e-issn2041-1723-
dc.rights.licensehttp://creativecommons.org/licenses/by/4.0/es_ES
dc.contributor.funderNorwegian Research Counciles_ES
dc.contributor.funderSouthern and Eastern Norway Regional Health Authorityes_ES
dc.contributor.funderNova Southeastern Universityes_ES
dc.contributor.funderSwedish Society for Medical Researches_ES
dc.contributor.funderFundación la Caixaes_ES
dc.contributor.funderEuropean Commissiones_ES
dc.contributor.funderInstituto de Salud Carlos IIIes_ES
dc.contributor.funderEuropean Institute of Innovation and Technologyes_ES
dc.contributor.funderJosep Carreras Leukemia Foundationes_ES
dc.contributor.funderCentres de Recerca de Catalunyaes_ES
dc.contributor.funderGeneralitat de Catalunyaes_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003748es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100002809es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004587es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100005677es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100005416es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000811es_ES
dc.identifier.pmid37291203-
dc.identifier.scopus2-s2.0-85161398175-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85161398175-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.cerifentitytypePublications-
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item.openairetypeartículo-
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item.languageiso639-1en-
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