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CXCR3 Identifies Human Naive CD8(+) T Cells with Enhanced Effector Differentiation Potential

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14740%2F19%3A00113376" target="_blank" >RIV/00216224:14740/19:00113376 - isvavai.cz</a>

  • Result on the web

    <a href="https://www.jimmunol.org/content/203/12/3179" target="_blank" >https://www.jimmunol.org/content/203/12/3179</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.4049/jimmunol.1901072" target="_blank" >10.4049/jimmunol.1901072</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    CXCR3 Identifies Human Naive CD8(+) T Cells with Enhanced Effector Differentiation Potential

  • Original language description

    In mice, the ability of naive T (T-N) cells to mount an effector response correlates with TCR sensitivity for self-derived Ags, which can be quantified indirectly by measuring surface expression levels of CD5. Equivalent findings have not been reported previously in humans. We identified two discrete subsets of human CD8(+) T-N cells, defined by the absence or presence of the chemokine receptor CXCR3. The more abundant CXCR3(+) T-N cell subset displayed an effector-like transcriptional profile and expressed TCRs with physicochemical characteristics indicative of enhanced interactions with peptide-HLA class I Ags. Moreover, CXCR3(+) T-N cells frequently produced IL-2 and TNF in response to nonspecific activation directly ex vivo and differentiated readily into Ag-specific effector cells in vitro. Comparative analyses further revealed that human CXCR3(+) T-N cells were transcriptionally equivalent to murine CXCR3(+) T-N cells, which expressed high levels of CD5. These findings provide support for the notion that effector differentiation is shaped by heterogeneity in the preimmune repertoire of human CD8(+) T cells.

  • 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

    30102 - Immunology

Result continuities

  • Project

    <a href="/en/project/LQ1601" target="_blank" >LQ1601: CEITEC 2020</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2019

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Journal of immunology

  • ISSN

    0022-1767

  • e-ISSN

  • Volume of the periodical

    203

  • Issue of the periodical within the volume

    12

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    11

  • Pages from-to

    3179-3189

  • UT code for WoS article

    000501838100012

  • EID of the result in the Scopus database

    2-s2.0-85076332121