All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

CD8(+) Tregs revisited: A heterogeneous population with different phenotypes and properties

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F21%3A00544971" target="_blank" >RIV/68378050:_____/21:00544971 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11310/21:10438694

  • Result on the web

    <a href="https://onlinelibrary.wiley.com/doi/10.1002/eji.202048614" target="_blank" >https://onlinelibrary.wiley.com/doi/10.1002/eji.202048614</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/eji.202048614" target="_blank" >10.1002/eji.202048614</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    CD8(+) Tregs revisited: A heterogeneous population with different phenotypes and properties

  • Original language description

    Regulatory T cells (Tregs) play a key role in the peripheral self-tolerance and preventing autoimmunity. While classical CD4(+) Foxp3(+) Tregs are well established, their CD8(+) counterparts are still controversial in many aspects including their phenotypic identity and their mechanisms of suppression. Because of these controversies and because of only a limited number of studies documenting the immunoregulatory function of CD8(+) Tregs in vivo, the concept of CD8(+) Tregs is still not unanimously accepted. We propose that any T-cell subset considered as true regulatory must be distinguishable from other cell types and must suppress in vivo immune responses via a known mechanism. In this article, we revisit the concept of CD8(+) Tregs by focusing on the characterization of individual CD8(+) T-cell subsets with proposed regulatory capacity separately. Therefore, we review the phenotype and function of CD8(+) FOXP3(+) T cells, CD8(+) CD122(+) T cells, CD8(+) CD28(low/-) T cells, CD8(+) CD45RC(low) T cells, T cells expressing CD8 alpha alpha homodimer and Qa-1-restricted CD8(+) T cells to show whether there is sufficient evidence to establish these subsets as bona fide Tregs. Based on the intrinsic ability of CD8(+) Treg subsets to promote immune tolerance in animal models, we elaborate on their potential use in clinics.

  • 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/GJ19-03435Y" target="_blank" >GJ19-03435Y: Naïve, memory, and virtual memory T cells in adaptive immune responses</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

    European Journal of Immunology

  • ISSN

    0014-2980

  • e-ISSN

    1521-4141

  • Volume of the periodical

    51

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    19

  • Pages from-to

    512-530

  • UT code for WoS article

    000619568300001

  • EID of the result in the Scopus database