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”

UNCOVERING THE DIFFERENCES BETWEEN RESPIRATORY PATHOGEN-INDUCED T-CELLS

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F23%3A00580718" target="_blank" >RIV/68378050:_____/23:00580718 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388971:_____/23:00580718

  • Result on the web

    <a href="http://ccsss.cz/index.php/ccsss/issue/view/41" target="_blank" >http://ccsss.cz/index.php/ccsss/issue/view/41</a>

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    UNCOVERING THE DIFFERENCES BETWEEN RESPIRATORY PATHOGEN-INDUCED T-CELLS

  • Original language description

    The upper respiratory tract (URT) is a site of entry for many public health-concerning pathogens such as SARS-CoV-2 (ref.1),the Influenza virus2, or Bordetella pertussis3. Although the URT represents an important site for initiating and transmitting infection, understanding the site-specific immunity in the nasal tissue during different infections is limited. So far, most works focused on respiratory infections have been concerned only with the lower respiratory tract (LRT)2. The adaptive immune system of URT consists of nasal-associated lymphoid tissue, which is a highly organized lymphoid structure with T and B cell areas and dispersed Tissue-resident memory T cells (Trm). Trm cells are a subset of memory T cells, which reside in non-lymphoid tissues, where they can act as alarm sensors in the immune surveillance network or as cytotoxic cells. Due to their advantageous location, they can be part of the first line of defense against many infections. The mechanism of development and the diversity and function of Trm cells are not yet completely understood4. We hypothesize that different infections such as intracellular viral infection or extracellular bacterial infection give rise to phenotypically and functionally distinct T-cell subsets. Moreover, CD4+and CD8+Trm cells induced by these infections might differ in their ability to persist in URT or LRT and respond to re-infection. To address this hypothesis we utilized two infection models: viral infection (Influenza A) and bacterial infection (Bordetella pertussis). We were able to identify various key differences between these two infections which will be further studied.

  • Czech name

  • Czech description

Classification

  • Type

    O - Miscellaneous

  • CEP classification

  • OECD FORD branch

    30102 - Immunology

Result continuities

  • Project

    <a href="/en/project/LX22NPO5103" target="_blank" >LX22NPO5103: National Institute of Virology and Bacteriology</a><br>

  • 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