Pregled bibliografske jedinice broj: 1156457
REGULACIJSKI LIMFOCITI T U LIMFOMAGENEZI
REGULACIJSKI LIMFOCITI T U LIMFOMAGENEZI // Zbornik sažetaka SBERS 2020
Banja Luka, Bosna i Hercegovina, 2020. str. 92-93 (predavanje, međunarodna recenzija, sažetak, ostalo)
CROSBI ID: 1156457 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
REGULACIJSKI LIMFOCITI T U LIMFOMAGENEZI
(REGULATORY T-LYMPHOCYTES IN LYMPHOMAGENESIS)
Autori
Gršković, Paula ; Gašparov, Slavko ; Ostojić Kolonić, Slobodanka ; Dotlić, Snježana ; Hančić, Suzana ; Dominis, Mara ; Korać, Petra
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, ostalo
Izvornik
Zbornik sažetaka SBERS 2020
/ - , 2020, 92-93
Skup
IV Simpozijum biologa i ekologa Republike Srpske
Mjesto i datum
Banja Luka, Bosna i Hercegovina, 12.11.2020. - 14.11.2020
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
B-limfomi, transkripcijski faktor FOXP3, tumorski mikrookoliš
(B lymphoma, transcriptional factor FOXP3, tumour microenvironment)
Sažetak
B-cell lymphomas are a heterogenous group of tumours that account for 85% of all non-Hodgkin lymphomas (NHL), tumours derived from cells of lymphoid lineage. B-lymphomas originate from various developmental stages of B lymphocytes. Classical Hodgkin’s lymphoma (cHL) also originates from B lymphocytes. Helper T lymphocytes expressing the transcription factor FOXP3 (CD4+ FOXP3+), also known as regulatory T lymphocytes (Tregs), are a component of tumour microenvironment (TME). FOXP3 regulates expression of various genes in Tregs responsible for the maintaining of immune tolerance and homeostasis of the immune system. It has been shown that Tregs influence the behaviour of tumour cells. The aim of this study was to evaluate the importance of Tregs in the most common groups of Blymphomas (follicular lymphoma (FL), mantle cell lymphoma (MCL), diffuse large B cell lymphoma (DLBCL)) and in classical Hodgkin’s lymphoma. Origin of the tumour cells was determined by the detection of markers like CD20 by immunohistochemical staining in formalin- fixed, paraffinembedded tissue samples. The same method was applied to evaluate the contents of TME based on markers CD68, CD3, CD4, CD8, PD-1, FOXP3, CD14, CD21. Statistically significant correlation between the numbers of Tregs and macrophages in TME was observed in MCL. Inverse correlation between the numbers of Tregs and cells expressing PD-1 was observed in cHL. No statistically significant correlation between the number of Tregs and the survival of the patients was observed in studied types of B-cell originated lymphoma. These results suggest that Tregs affect the contents of TME in Bcell originated lymphoma.
Izvorni jezik
Engleski
Znanstvena područja
Biologija, Temeljne medicinske znanosti
POVEZANOST RADA
Ustanove:
Klinička bolnica "Merkur",
Medicinski fakultet, Zagreb,
Prirodoslovno-matematički fakultet, Zagreb
Profili:
Slobodanka Ostojić Kolonić
(autor)
Suzana Hančić
(autor)
Petra Korać
(autor)
Marija Dominis
(autor)
Paula Gršković
(autor)
Slavko Gašparov
(autor)