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IL-35, an anti-inflammatory cytokine which expands CD4+CD25+ Treg Cells

Articolo
Data di Pubblicazione:
2010
Citazione:
IL-35, an anti-inflammatory cytokine which expands CD4+CD25+ Treg Cells / Castellani, Ml; Anogeianaki, A; Felaco, P; Toniato, E; De Lutiis, Ma; Shaik, B; Fulcheri, M; Vecchiet, J; Tetè, S; Salini, V; Theoharides, Tc; Caraffa, A; Antinolfi, P; Frydas, I; Conti, P; Cuccurullo, C; Ciampoli, C; Cerulli, G; Kempuraj, D. - In: JOURNAL OF BIOLOGICAL REGULATORS & HOMEOSTATIC AGENTS. - ISSN 0393-974X. - 24:2(2010), pp. 131-135.
Abstract:
Interleukin 12 (IL 12) p35/p40 is a heterodimeric cytokine which plays a critical role in inflammation, immunity and tissue proliferation, and also plays a relevant function in T helper (Th) cell polarization and Th1 T-cell differentiation. IL-12 family members, IL-12p70, IL-23, IL-27 and IL-35, play an important role in influencing helper T-cell differentiation. EBV-induced gene 3 can be associated with the p35 subunit of IL-12 to form the EBI3/p35 heterodimer, also called IL-35. It has been shown that IL-35 has biological activity and able to expand CD4+CD25+ Treg cells, suppress the proliferation of CD4+CD25- effector cells and inhibit Th17 cell polarization. IL-35 has been shown to be constitutively expressed by regulatory T (Treg) cells CD4(+)CD25(+)Foxp3(+) and suggested to contribute to their suppressive activity. IL-35 is a crucial mediator which provokes CD4+CD25+ T cell proliferation and IL-10 generation, another well-known anti-inflammatory cytokine, along with TGFbeta cytokine. These studies suggest that IL-35, together with other successfully discovered cytokine inhibitors, represents a new potential therapeutic cytokine for chronic inflammation, autoimmunity and other immunological disorders.
Tipologia CRIS:
1.1 Articolo in rivista
Elenco autori:
Castellani, Ml; Anogeianaki, A; Felaco, P; Toniato, E; De Lutiis, Ma; Shaik, B; Fulcheri, M; Vecchiet, J; Tetè, S; Salini, V; Theoharides, Tc; Caraffa, A; Antinolfi, P; Frydas, I; Conti, P; Cuccurullo, C; Ciampoli, C; Cerulli, G; Kempuraj, D
Autori di Ateneo:
SALINI VINCENZO
Link alla scheda completa:
https://iris.unisr.it/handle/20.500.11768/87061
Pubblicato in:
JOURNAL OF BIOLOGICAL REGULATORS & HOMEOSTATIC AGENTS
Journal
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