TCRζdimlymphocytes define populations of circulating effector cells that migrate to inflamed tissues

The T-cell receptor ζ (TCRζ) chain is a master sensor and regulator of lymphocyte responses. Loss of TCRζ expression has been documented in infectious, inflammatory, and malignant diseases, suggesting that it may serve to limit T-cell reactivity and effector responses at sites of tissue damage. Thes...

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Veröffentlicht in:Blood 2007-05, Vol.109 (10), p.4328-4335
Hauptverfasser: Zhang, Zhuoli, Gorman, Claire L., Vermi, Anna-Chiara, Monaco, Claudia, Foey, Andrew, Owen, Sally, Amjadi, Parisa, Vallance, Alena, McClinton, Catherine, Marelli-Berg, Federica, Isomäki, Pia, Russell, Andrew, Dazzi, Francesco, Vyse, Timothy J., Brennan, Fionula M., Cope, Andrew P.
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Sprache:eng
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Zusammenfassung:The T-cell receptor ζ (TCRζ) chain is a master sensor and regulator of lymphocyte responses. Loss of TCRζ expression has been documented in infectious, inflammatory, and malignant diseases, suggesting that it may serve to limit T-cell reactivity and effector responses at sites of tissue damage. These observations prompted us to explore the relationship between TCRζ expression and effector function in T cells. We report here that TCRζdim lymphocytes are enriched for antigen-experienced cells refractory to TCR-induced proliferation. Compared to their TCRζbright counterparts, TCRζdim cells share characteristics of differentiated effector T cells but use accessory pathways for transducing signals for inflammatory cytokine gene expression and cell contact-dependent pathways to activate monocytes. TCRζdim T cells accumulate in inflamed tissues in vivo and have intrinsic migratory activity in vitro. Whilst blocking leukocyte trafficking with anti-TNF therapy in vivo is associated with the accumulation of TCRζdim T cells in peripheral blood, this T-cell subset retains the capacity to migrate in vitro. Taken together, the functional properties of TCRζdim T cells make them promising cellular targets for the treatment of chronic inflammatory disease.
ISSN:0006-4971
1528-0020
DOI:10.1182/blood-2006-12-064170