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TIM-3 levels correlate with enhanced NK cell cytotoxicity and improved clinical outcome in AML patients

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023736%3A_____%2F21%3A00013231" target="_blank" >RIV/00023736:_____/21:00013231 - isvavai.cz</a>

  • Alternative codes found

    RIV/00669806:_____/21:10425780 RIV/00216208:11140/21:10425780 RIV/00216208:11110/21:10425780 RIV/00064203:_____/21:10425780 RIV/00216208:11130/21:10425780

  • Result on the web

    <a href="https://doi.org/10.1080/2162402X.2021.1889822" target="_blank" >https://doi.org/10.1080/2162402X.2021.1889822</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1080/2162402X.2021.1889822" target="_blank" >10.1080/2162402X.2021.1889822</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    TIM-3 levels correlate with enhanced NK cell cytotoxicity and improved clinical outcome in AML patients

  • Original language description

    Accumulating evidence indicates that immune checkpoint inhibitors (ICIs) can restore CD8+ cytotoxic T lymphocyte (CTL) functions in preclinical models of acute myeloid leukemia (AML). However, ICIs targeting programmed cell death 1 (PDCD1, best known as PD-1) and cytotoxic T lymphocyte-associated protein 4 (CTLA4) have limited clinical efficacy in patients with AML. Natural killer (NK) cells are central players in AML-targeting immune responses. However, little is known on the relationship between co-inhibitory receptors expressed by NK cells and the ability of the latter to control AML. Here, we show that hepatitis A virus cellular receptor 2 (HAVCR2, best known as TIM-3) is highly expressed by NK cells from AML patients, correlating with improved functional licensing and superior effector functions. Altogether, our data indicate that NK cell frequency as well as TIM-3 expression levels constitute prognostically relevant biomarkers of active immunity against 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

    30205 - Hematology

Result continuities

  • Project

    <a href="/en/project/NV18-03-00277" target="_blank" >NV18-03-00277: Polymorphisms in the NK cells receptors and their ligands within the Czech population</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2021

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    OncoImmunology

  • ISSN

    2162-4011

  • e-ISSN

  • Volume of the periodical

    10

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    12

  • Pages from-to

    "art. no. e1889822"

  • UT code for WoS article

    000627790900001

  • EID of the result in the Scopus database

    2-s2.0-85102181179