Počet záznamů: 1  

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
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevNovel PD-L1- and collagen-expressing patient-derived cell line of undifferentiated pleomorphic sarcoma (JBT19) as a model for cancer immunotherapy.
    Tvůrce(i) 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)
    Zdroj.dok.Scientific Reports. - : Nature Publishing Group - ISSN 2045-2322
    Roč. 13, November (2023), s. 19079
    Poč.str.20 s.
    Jazyk dok.eng - angličtina
    Země vyd.US - Spojené státy americké
    Klíč. slovaB7-H1 Antigen ; Histiocytoma ; Immunotherapy ; ligand ; programmed death 1 ligand 1 ; malignant fibrous histiocytoma ; cell line ; nude mouse
    Obor OECDImmunology
    CEPNU23-08-00071 GA MZd - Ministerstvo zdravotnictví
    LX22NPO5102 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    LM2018129 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    EF18_046/0016045 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    Způsob publikováníOpen access
    Institucionální podporaMBU-M - RVO:61388971 ; UMG-J - RVO:68378050
    UT WOS001099663700027
    EID SCOPUS85175859406
    DOI10.1038/s41598-023-46305-7
    AnotaceSoft 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.
    PracovištěMikrobiologický ústav
    KontaktEliška Spurná, eliska.spurna@biomed.cas.cz, Tel.: 241 062 231
    Rok sběru2024
    Elektronická adresahttps://www.nature.com/articles/s41598-023-46305-7
Počet záznamů: 1  

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