Pregled bibliografske jedinice broj: 765879
IL-33-dependent immunosuppressive Treg responses to liver damage during MCMV infection
IL-33-dependent immunosuppressive Treg responses to liver damage during MCMV infection // 3rd Belgrade EFIS Abstract book
Aranđelovac, Srbija, 2015. (predavanje, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 765879 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
IL-33-dependent immunosuppressive Treg responses to liver damage during MCMV infection
Autori
Branka Popović, Mijo Golemac, Lidija Bilić- Zulle, Miodrag Lukić, Astrid Krmpotić, Stipan Jonjić
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
3rd Belgrade EFIS Abstract book
/ - , 2015
Skup
3rd Belgrade EFIS Symposium on Immunoregulation
Mjesto i datum
Aranđelovac, Srbija, 24.05.2015. - 27.05.2015
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Interleukin-33; mouse; mouse cytomegalovirus; ST2 protein; mouse; T-lymphocytes; regulatory
Sažetak
Regulatory T cells (Treg) are critical for preventing autoimmunity mediated by self- reactive T cells, but also in modulating immune responses to infections and therefore controlling balance between activation and tolerance. Murine cytomegalovirus (MCMV) is a herpesvirus with pathogenic potential that can induce high levels of viral replication and modulate antiviral responses. Thus, early immune mechanisms are essential in controlling virus replication and protecting the host from virus-induced pathology. Studies on Treg cells reveal their role in suppressing early NK and T cell responses activated by MCMV infection. However, absence of Treg cells does not influence viral clearance. Here we show that Treg cells are indispensable for preventing liver pathology induced by MCMV infection. In addition, their suppressive capacity is dependent on tissue alarmin, IL-33, which promotes Treg recruitment and function in liver of MCMV infected mice. Moreover, mice lacking IL-33 receptor, showed higher death rate mediated by stronger liver pathology after infection with high viral dose. This is a consequence of decreased infiltration of Treg cells and lower expression of anti-inflammatory IL-10 and TGF-β, compared to control mice. In the light of recent discovery of IL-33's importance for accumulation and maintenance of Treg cells in acute colitis model, our results suggest protective and homeostatic role of IL- 33 signaling in inflammation induced by MCMV infection.
Izvorni jezik
Engleski
POVEZANOST RADA
Profili:
Lidija Bilić-Zulle
(autor)
Mijo Golemac
(autor)
Astrid Krmpotić
(autor)
Stipan Jonjić
(autor)
Branka Popović
(autor)