IFN-λs mediate antiviral protection through a distinct class II cytokine receptor complex

We report here the identification of a ligand-receptor system that, upon engagement, leads to the establishment of an antiviral state. Three closely positioned genes on human chromosome 19 encode distinct but paralogous proteins, which we designate interferon-λ1 (IFN-λ1), IFN-λ2 and IFN-λ3 (tentativ...

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Veröffentlicht in:Nature immunology 2003-01, Vol.4 (1), p.69-77
Hauptverfasser: Kotenko, Sergei V., Gallagher, Grant, Baurin, Vitaliy V., Lewis-Antes, Anita, Shen, Meiling, Shah, Nital K., Langer, Jerome A., Sheikh, Faruk, Dickensheets, Harold, Donnelly, Raymond P.
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Sprache:eng
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Zusammenfassung:We report here the identification of a ligand-receptor system that, upon engagement, leads to the establishment of an antiviral state. Three closely positioned genes on human chromosome 19 encode distinct but paralogous proteins, which we designate interferon-λ1 (IFN-λ1), IFN-λ2 and IFN-λ3 (tentatively designated as IL-29, IL-28A and IL-28B, respectively, by HUGO). The expression of IFN-λ mRNAs was inducible by viral infection in several cell lines. We identified a distinct receptor complex that is utilized by all three IFN-λ proteins for signaling and is composed of two subunits, a receptor designated CRF2-12 (also designated as IFN-λR1) and a second subunit, CRF2-4 (also known as IL-10R2). Both receptor chains are constitutively expressed on a wide variety of human cell lines and tissues and signal through the Jak-STAT (Janus kinases–signal transducers and activators of transcription) pathway. This receptor-ligand system may contribute to antiviral or other defenses by a mechanism similar to, but independent of, type I IFNs.
ISSN:1529-2908
1529-2916
DOI:10.1038/ni875