Immune cell profiling of the cerebrospinal fluid enables the characterization of the brain metastasis microenvironment

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  • dc.contributor.author Rubio Pérez, Carlota
  • dc.contributor.author Trincado Alonso, Juan Luis, 1987-
  • dc.contributor.author Marchese, Domenica, 1986-
  • dc.contributor.author Moutinho, Catia
  • dc.contributor.author Ruiz, Sara
  • dc.contributor.author Parra Farré, Genís
  • dc.contributor.author Heyn, Holger
  • dc.contributor.author Seoane, Joan
  • dc.date.accessioned 2021-05-25T12:23:10Z
  • dc.date.available 2021-05-25T12:23:10Z
  • dc.date.issued 2021
  • dc.description.abstract Brain metastases are the most common tumor of the brain with a dismal prognosis. A fraction of patients with brain metastasis benefit from treatment with immune checkpoint inhibitors (ICI) and the degree and phenotype of the immune cell infiltration has been used to predict response to ICI. However, the anatomical location of brain lesions limits access to tumor material to characterize the immune phenotype. Here, we characterize immune cells present in brain lesions and matched cerebrospinal fluid (CSF) using single-cell RNA sequencing combined with T cell receptor genotyping. Tumor immune infiltration and specifically CD8+ T cell infiltration can be discerned through the analysis of the CSF. Consistently, identical T cell receptor clonotypes are detected in brain lesions and CSF, confirming cell exchange between these compartments. The analysis of immune cells of the CSF can provide a non-invasive alternative to predict the response to ICI, as well as identify the T cell receptor clonotypes present in brain metastasis.
  • dc.description.sponsorship The study was undertaken with the support of the Fundación Asociación Española contra el Cáncer (AECC), FERO (EDM), Ramón Areces Foundation, Cellex Foundation, BBVA (CAIMI), the ISCIII, FIS (PI16/01278), the Ministerio de Ciencia, Innovación y Universidades (SAF2017-89109-P; AEI/FEDER, UE), the Juan de la Cierva formación fellowship (C.R.-P. and L.E.), Sara Borrell fellowship (E.P-R.). We acknowledge support of the Spanish Ministry of Science and Innovation to the EMBL partnership, the Centro de Excelencia Severo Ochoa and the CERCA Program/Generalitat de Catalunya. We also acknowledge the support of the Spanish Ministry of Science and Innovation through the Instituto de Salud Carlos III, the Generalitat de Catalunya through Departament de Salut and Departament d’Empresa i Coneixement, and the Co-financing by the Spanish Ministry of Ministry of Science and Innovation with funds from the European Regional Development Fund (ERDF) corresponding to the 2014–2020 Smart Growth Operating Program
  • dc.format.mimetype application/pdf
  • dc.identifier.citation Rubio-Perez C, Planas-Rigol E, Trincado JL, Bonfill-Teixidor E, Arias A, Marchese D et al. Immune cell profiling of the cerebrospinal fluid enables the characterization of the brain metastasis microenvironment. Nat Comm. 2021 Mar 8;12(1):1503. DOI: 10.1038/s41467-021-21789-x
  • dc.identifier.doi http://dx.doi.org/10.1038/s41467-021-21789-x
  • dc.identifier.issn 2041-1723
  • dc.identifier.uri http://hdl.handle.net/10230/47651
  • dc.language.iso eng
  • dc.publisher Nature Research
  • dc.relation.projectID info:eu-repo/grantAgreement/ES/2PE/SAF2017-89109-P
  • dc.rights © Carlota Rubio-Perez et al. 2021. This article is licensed under a Creative CommonsAttribution 4.0 International License, which permits use, sharing,adaptation, distribution and reproduction in any medium or format, as long as you giveappropriate credit to the original author(s) and the source, provide a link to the CreativeCommons license, and indicate if changes were made (https://creativecommons.org/licenses/by/4.0/)
  • dc.rights.accessRights info:eu-repo/semantics/openAccess
  • dc.subject.other Sistema nerviós -- Càncer
  • dc.subject.other Metàstasi
  • dc.subject.other Genètica
  • dc.title Immune cell profiling of the cerebrospinal fluid enables the characterization of the brain metastasis microenvironment
  • dc.type info:eu-repo/semantics/article
  • dc.type.version info:eu-repo/semantics/publishedVersion