2021
Rituximab induces rapid blood repopulation by CLL cells mediated through their release from immune niches and complement exhaustion
BORSKÝ, Marek, Viera HRABČÁKOVÁ, Jitka NOVOTNÁ, Yvona BRYCHTOVÁ, Michael DOUBEK et. al.Základní údaje
Originální název
Rituximab induces rapid blood repopulation by CLL cells mediated through their release from immune niches and complement exhaustion
Autoři
BORSKÝ, Marek (203 Česká republika, domácí), Viera HRABČÁKOVÁ (703 Slovensko, domácí), Jitka NOVOTNÁ (203 Česká republika, domácí), Yvona BRYCHTOVÁ (203 Česká republika, domácí), Michael DOUBEK (203 Česká republika, domácí), Anna PANOVSKÁ (203 Česká republika, domácí), Petr MULLER (203 Česká republika), Jiří MAYER (203 Česká republika, domácí), Martin TRBUŠEK (203 Česká republika, garant, domácí) a Marek MRÁZ (203 Česká republika, domácí)
Vydání
Leukemia Research, OXFORD, PERGAMON-ELSEVIER SCIENCE LTD, 2021, 0145-2126
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30205 Hematology
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 3.715
Kód RIV
RIV/00216224:14110/21:00124279
Organizační jednotka
Lékařská fakulta
UT WoS
000703570900003
Klíčová slova anglicky
Chronic lymphocytic leukemia/CLL; Rituximab; Complement; Recrudescence; Peripheral blood repopulation
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 4. 3. 2022 09:52, Mgr. Pavla Foltynová, Ph.D.
Anotace
V originále
The in vivo rituximab effects in B cell malignancies are only partially understood. Here we analyzed in a large chronic lymphocytic leukemia (CLL) cohort (n = 80) the inter-patient variability in CLL cell count reduction within the first 24 h of rituximab administration in vivo, and a phenomenon of blood repopulation by malignant cells after anti-CD20 antibody therapy. Larger CLL cell elimination after rituximab infusion was associated with lower pre-therapy CLL cell counts, higher CD20 levels, and the non-exhausted capacity of complement dependent cytotoxicity (CDC). The absolute amount of cell-surface CD20 molecules (CD20 density x CLL lymphocytosis) was a predictor for complement exhaustion during therapy. We also describe that a highly variable decrease in CLL cell counts at 5 h (88 %-2%) following rituximab infusion is accompanied in most patients by peripheral blood repopulation with CLL cells at 24 h, and in similar to 20 % of patients, this resulted in CLL counts higher than before therapy. We provide evidence that CLL cells recrudescence is linked with i) CDC exhaustion, which leads to the formation of an insufficient amount of membrane attack complexes, likely resulting in temporary retention of surviving rituximab-opsonized cells by the mononuclear-phagocyte system (followed by their release back to blood), and ii) CLL cells regression from immune niches (CXCR4(dim)CD5(bright) intraclonal subpopulation). Patients with major peripheral blood CLL cell repopulation exhibited a longer time to-progression after chemoimmunotherapy compared to patients with lower or no repopulation, suggesting chemotherapy vulnerability of CLL cells that repopulate the blood.