Mature dendritic cells correlate with favorable immune infiltrate and improved prognosis in ovarian carcinoma patients
Jazyk angličtina Země Velká Británie, Anglie Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
30526667
PubMed Central
PMC6288908
DOI
10.1186/s40425-018-0446-3
PII: 10.1186/s40425-018-0446-3
Knihovny.cz E-zdroje
- Klíčová slova
- CD8+ cytotoxic T lymphocytes, DC-LAMP, Dendritic cells, Natural killer cells, Tertiary lymphoid structures,
- MeSH
- biologické markery MeSH
- dendritické buňky imunologie metabolismus patologie MeSH
- dospělí MeSH
- imunofenotypizace MeSH
- imunohistochemie MeSH
- Kaplanův-Meierův odhad MeSH
- karcinom imunologie mortalita patologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádorové mikroprostředí imunologie MeSH
- nádory vaječníků imunologie mortalita patologie terapie MeSH
- prognóza MeSH
- proporcionální rizikové modely MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- staging nádorů MeSH
- T-lymfocyty - podskupiny imunologie metabolismus patologie MeSH
- tumor infiltrující lymfocyty imunologie metabolismus patologie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- biologické markery MeSH
A high density of tumor-infiltrating CD8+ T cells and CD20+ B cells correlates with prolonged survival in patients with a wide variety of human cancers, including high-grade serous ovarian carcinoma (HGSC). However, the potential impact of mature dendritic cells (DCs) in shaping the immune contexture of HGSC, their role in the establishment of T cell-dependent antitumor immunity, and their potential prognostic value for HGSC patients remain unclear. We harnessed immunohistochemical tests and biomolecular analyses to demonstrate that a high density of tumor-infiltrating DC-LAMP+ DCs is robustly associated with an immune contexture characterized by TH1 polarization and cytotoxic activity. We showed that both mature DCs and CD20+ B cells play a critical role in the generation of a clinically-favorable cytotoxic immune response in HGSC microenvironment. In line with this notion, robust tumor infiltration by both DC-LAMP+ DCs and CD20+ B cells was associated with most favorable overall survival in two independent cohorts of chemotherapy-naïve HGSC patients. Our findings suggest that the presence of mature, DC-LAMP+ DCs in the tumor microenvironment may represent a novel, powerful prognostic biomarker for HGSC patients that reflects the activation of clinically-relevant anticancer immunity.
Department of Radiation Oncology Weill Cornell Medical College New York NY USA
INSERM U1138 Centre de Recherche des Cordeliers Paris France
Sandra and Edward Meyer Cancer Center New York NY USA
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