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Regulatory T cells suppress the formation of potent KLRK1 and IL- 7R expressing effector CD8 T cells by limiting IL-2

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F23%3A00569557" target="_blank" >RIV/68378050:_____/23:00569557 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388971:_____/23:00569557 RIV/00216208:11310/23:10479727

  • Result on the web

    <a href="https://elifesciences.org/articles/79342" target="_blank" >https://elifesciences.org/articles/79342</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.7554/eLife.79342" target="_blank" >10.7554/eLife.79342</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Regulatory T cells suppress the formation of potent KLRK1 and IL- 7R expressing effector CD8 T cells by limiting IL-2

  • Original language description

    Regulatory T cells (Tregs) are indispensable for maintaining self-tolerance by suppressing conventional T cells. On the other hand, Tregs promote tumor growth by inhibiting anticancer immunity. In this study, we identified that Tregs increase the quorum of self-reactive CD8+ T cells required for the induction of experimental autoimmune diabetes in mice. Their major suppression mechanism is limiting available IL-2, an essential T-cell cytokine. Specifically, Tregs inhibit the formation of a previously uncharacterized subset of antigen-stimulated KLRK1+ IL-7R+ (KILR) CD8+ effector T cells, which are distinct from conventional effector CD8+ T cells. KILR CD8+ T cells show superior cell-killing abilities in vivo. The administration of agonistic IL-2 immunocomplexes phenocopies the absence of Tregs, i.e., it induces KILR CD8+ T cells, promotes autoimmunity, and enhances antitumor responses in mice. Counterparts of KILR CD8+ T cells were found in the human blood, revealing them as a potential target for immunotherapy.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>SC</sub> - Article in a specialist periodical, which is included in the SCOPUS database

  • CEP classification

  • OECD FORD branch

    30102 - Immunology

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

    eLife

  • ISSN

    2050-084X

  • e-ISSN

    2050-084X

  • Volume of the periodical

    12

  • Issue of the periodical within the volume

    Jan 27

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    30

  • Pages from-to

    e79342

  • UT code for WoS article

    000941583600001

  • EID of the result in the Scopus database

    2-s2.0-85147108371