Complement regulator CD46 temporally regulates cytokine production by conventional and unconventional T cells View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2010-09

AUTHORS

John Cardone, Gaelle Le Friec, Pierre Vantourout, Andrew Roberts, Anja Fuchs, Ian Jackson, Tesha Suddason, Graham Lord, John P Atkinson, Andrew Cope, Adrian Hayday, Claudia Kemper

ABSTRACT

In this study we demonstrate a new form of immunoregulation: engagement on CD4(+) T cells of the complement regulator CD46 promoted the effector potential of T helper type 1 cells (T(H)1 cells), but as interleukin 2 (IL-2) accumulated, it switched cells toward a regulatory phenotype, attenuating IL-2 production via the transcriptional regulator ICER/CREM and upregulating IL-10 after interaction of the CD46 tail with the serine-threonine kinase SPAK. Activated CD4(+) T cells produced CD46 ligands, and blocking CD46 inhibited IL-10 production. Furthermore, CD4(+) T cells in rheumatoid arthritis failed to switch, consequently producing excessive interferon-gamma (IFN-gamma). Finally, gammadelta T cells, which rarely produce IL-10, expressed an alternative CD46 isoform and were unable to switch. Nonetheless, coengagement of T cell antigen receptor (TCR) gammadelta and CD46 suppressed effector cytokine production, establishing that CD46 uses distinct mechanisms to regulate different T cell subsets during an immune response. More... »

PAGES

862

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/ni.1917

DOI

http://dx.doi.org/10.1038/ni.1917

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1039016877

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/20694009


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