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Novel PD-L1- and collagen-expressing patient-derived cell line of undifferentiated pleomorphic sarcoma (JBT19) as a model for cancer immunotherapy.

  1. 1.
    SYSNO ASEP0578397
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleNovel PD-L1- and collagen-expressing patient-derived cell line of undifferentiated pleomorphic sarcoma (JBT19) as a model for cancer immunotherapy.
    Author(s) Táborská, P. (CZ)
    Lukáč, Pavol (MBU-M) ORCID, RID
    Stakheev, Dmitry (MBU-M)
    Rajsiglová, Lenka (MBU-M) ORCID
    Kalkusová, K. (CZ)
    Strnadová, K. (CZ)
    Lacina, L. (CZ)
    Dvořánková, B. (CZ)
    Novotný, Jiří (UMG-J) ORCID
    Kolář, Michal (UMG-J) RID, ORCID
    Vraná, M. (CZ)
    Čechová, H. (CZ)
    Ransdorfová, S. (CZ)
    Valerianová, M. (CZ)
    Smetana Jr., K. (CZ)
    Vannucci, Luca (MBU-M) RID, ORCID
    Smrž, Daniel (MBU-M)
    Source TitleScientific Reports. - : Nature Publishing Group - ISSN 2045-2322
    Roč. 13, November (2023), s. 19079
    Number of pages20 s.
    Languageeng - English
    CountryUS - United States
    KeywordsB7-H1 Antigen ; Histiocytoma ; Immunotherapy ; ligand ; programmed death 1 ligand 1 ; malignant fibrous histiocytoma ; cell line ; nude mouse
    OECD categoryImmunology
    R&D ProjectsNU23-08-00071 GA MZd - Ministry of Health (MZ)
    LX22NPO5102 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    LM2018129 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    EF18_046/0016045 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Method of publishingOpen access
    Institutional supportMBU-M - RVO:61388971 ; UMG-J - RVO:68378050
    UT WOS001099663700027
    EID SCOPUS85175859406
    DOI10.1038/s41598-023-46305-7
    AnnotationSoft tissue sarcomas are aggressive mesenchymal-origin malignancies. Undifferentiated pleomorphic sarcoma (UPS) belongs to the aggressive, high-grade, and least characterized sarcoma subtype, affecting multiple tissues and metastasizing to many organs. The treatment of localized UPS includes surgery in combination with radiation therapy. Metastatic forms are treated with chemotherapy. Immunotherapy is a promising treatment modality for many cancers. However, the development of immunotherapy for UPS is limited due to its heterogeneity, antigenic landscape variation, lower infiltration with immune cells, and a limited number of established patient-derived UPS cell lines for preclinical research. In this study, we established and characterized a novel patient-derived UPS cell line, JBT19. The JBT19 cells express PD-L1 and collagen, a ligand of the immune checkpoint molecule LAIR-1. JBT19 cells can form spheroids in vitro and solid tumors in immunodeficient nude mice. We found JBT19 cells induce expansion of JBT19-reactive autologous and allogeneic NK, T, and NKT-like cells, and the reactivity of the expanded cells was associated with cytotoxic impact on JBT19 cells. The PD-1 and LAIR-1 ligand-expressing JBT19 cells show ex vivo immunogenicity and effective in vivo xenoengraftment properties that can offer a unique resource in the preclinical research developing novel immunotherapeutic interventions in the treatment of UPS.
    WorkplaceInstitute of Microbiology
    ContactEliška Spurná, eliska.spurna@biomed.cas.cz, Tel.: 241 062 231
    Year of Publishing2024
    Electronic addresshttps://www.nature.com/articles/s41598-023-46305-7
Number of the records: 1  

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