2021
Deciphering the complex circulating immune cell microenvironment in chronic lymphocytic leukaemia using patient similarity networks
MIKULKOVA, Zuzana, Gayane MANUKYAN, Peter TURCSANYI, Milos KUDELKA, Renata URBANOVA et. al.Základní údaje
Originální název
Deciphering the complex circulating immune cell microenvironment in chronic lymphocytic leukaemia using patient similarity networks
Autoři
MIKULKOVA, Zuzana (203 Česká republika), Gayane MANUKYAN, Peter TURCSANYI, Milos KUDELKA (203 Česká republika), Renata URBANOVA (203 Česká republika), Jakub SAVARA (203 Česká republika), Eliska OCHODKOVA (203 Česká republika), Yvona BRYCHTOVÁ (203 Česká republika, domácí), Jan MOLINSKY (203 Česká republika), Martin SIMKOVIC (203 Česká republika), David STAROSTKA (203 Česká republika), Jan NOVAK (203 Česká republika), Ondrej JANCA (203 Česká republika), Martin DIHEL (203 Česká republika), Pavlina RYZNEROVA (203 Česká republika), Lekaa MOHAMMAD, Tomas PAPAJIK (203 Česká republika) a Eva KRIEGOVA (203 Česká republika, garant)
Vydání
Nature Scientific Reports, London, NATURE RESEARCH, 2021, 2045-2322
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30205 Hematology
Stát vydavatele
Německo
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 4.996
Kód RIV
RIV/00216224:14110/21:00121640
Organizační jednotka
Lékařská fakulta
UT WoS
000627829300026
Klíčová slova anglicky
chronic lymphocytic leukaemia; complex circulating immune cell
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 24. 5. 2021 14:25, Mgr. Tereza Miškechová
Anotace
V originále
The tissue microenvironment in chronic lymphocytic leukaemia (CLL) plays a key role in the pathogenesis of CLL, but the complex blood microenvironment in CLL has not yet been fully characterised. Therefore, immunophenotyping of circulating immune cells in 244 CLL patients and 52 healthy controls was performed using flow cytometry and analysed by multivariate Patient Similarity Networks (PSNs). Our study revealed high inter-individual heterogeneity in the distribution and activation of bystander immune cells in CLL, depending on the bulk of the CLL cells. High CLL counts were associated with low activation on circulating monocytes and T cells and vice versa. The highest activation of immune cells, particularly of intermediate and non-classical monocytes, was evident in patients treated with novel agents. PSNs revealed a low activation of immune cells in CLL progression, irrespective of IgHV status, Binet stage and TP53 disruption. Patients with high intermediate monocytes (>5.4%) with low activation were 2.5 times more likely (95% confidence interval 1.421-4.403, P=0.002) to had shorter time-to-treatment than those with low monocyte counts. Our study demonstrated the association between the activation of circulating immune cells and the bulk of CLL cells. The highest activation of bystander immune cells was detected in patients with slow disease course and in those treated with novel agents. The subset of intermediate monocytes showed predictive value for time-to-treatment in CLL.