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Strong homeostatic TCR signals induce formation of self-tolerant virtual memory CD8 T cells

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F18%3A00495610" target="_blank" >RIV/68378050:_____/18:00495610 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.15252/embj.201798518" target="_blank" >http://dx.doi.org/10.15252/embj.201798518</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.15252/embj.201798518" target="_blank" >10.15252/embj.201798518</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Strong homeostatic TCR signals induce formation of self-tolerant virtual memory CD8 T cells

  • Original language description

    Virtual memory T cells are foreign antigen-inexperienced T cells that have acquired memory-like phenotype and constitute 10-20% of all peripheral CD8(+) T cells in mice. Their origin, biological roles, and relationship to naive and foreign antigen-experienced memory T cells are incompletely understood. By analyzing T-cell receptor repertoires and using retrogenic monoclonal T-cell populations, we demonstrate that the virtual memory T-cell formation is a so far unappreciated cell fate decision checkpoint. We describe two molecular mechanisms driving the formation of virtual memory T cells. First, virtual memory T cells originate exclusively from strongly self-reactive T cells. Second, the stoichiometry of the CD8 interaction with Lck regulates the size of the virtual memory T-cell compartment via modulating the self-reactivity of individual T cells. Although virtual memory T cells descend from the highly self-reactive clones and acquire a partial memory program, they are not more potent in inducing experimental autoimmune diabetes than naive T cells. These data underline the importance of the variable level of self-reactivity in polyclonal T cells for the generation of functional T-cell diversity.

  • 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

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

  • Continuities

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

Others

  • Publication year

    2018

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    EMBO Journal

  • ISSN

    0261-4189

  • e-ISSN

  • Volume of the periodical

    37

  • Issue of the periodical within the volume

    14

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    17

  • Pages from-to

  • UT code for WoS article

    000438517100006

  • EID of the result in the Scopus database