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Type I interferon signaling in malignant blasts contributes to treatment efficacy in AML patients

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F23%3A00571076" target="_blank" >RIV/68378050:_____/23:00571076 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388971:_____/23:00571076 RIV/00216208:11130/23:10458307 RIV/00216208:11110/23:10458307 RIV/00216208:11140/23:10458307 and 3 more

  • Result on the web

    <a href="https://www.nature.com/articles/s41419-023-05728-w" target="_blank" >https://www.nature.com/articles/s41419-023-05728-w</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1038/s41419-023-05728-w" target="_blank" >10.1038/s41419-023-05728-w</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Type I interferon signaling in malignant blasts contributes to treatment efficacy in AML patients

  • Original language description

    While type I interferon (IFN) is best known for its key role against viral infection, accumulating preclinical and clinical data indicate that robust type I IFN production in the tumor microenvironment promotes cancer immunosurveillance and contributes to the efficacy of various antineoplastic agents, notably immunogenic cell death inducers. Here, we report that malignant blasts from patients with acute myeloid leukemia (AML) release type I IFN via a Toll-like receptor 3 (TLR3)-dependent mechanism that is not driven by treatment. While in these patients the ability of type I IFN to stimulate anticancer immune responses was abolished by immunosuppressive mechanisms elicited by malignant blasts, type I IFN turned out to exert direct cytostatic, cytotoxic and chemosensitizing activity in primary AML blasts, leukemic stem cells from AML patients and AML xenograft models. Finally, a genetic signature of type I IFN signaling was found to have independent prognostic value on relapse-free survival and overall survival in a cohort of 132 AML patients. These findings delineate a clinically relevant, therapeutically actionable and prognostically informative mechanism through which type I IFN mediates beneficial effects in patients with AML.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10601 - Cell biology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2023

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Cell Death & Disease

  • ISSN

    2041-4889

  • e-ISSN

    2041-4889

  • Volume of the periodical

    14

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    12

  • Pages from-to

    209

  • UT code for WoS article

    000958731000002

  • EID of the result in the Scopus database

    2-s2.0-85150979168