2021
The impact of lymphocytosis and CD4/CD8 ratio on the anti-JCV antibody index and clinical data in patients treated with natalizumab
KOLČAVA, Jan, Monika HULOVÁ, Lucie ŘÍHOVÁ, Josef BEDNAŘÍK, Pavel ŠTOURAČ et. al.Základní údaje
Originální název
The impact of lymphocytosis and CD4/CD8 ratio on the anti-JCV antibody index and clinical data in patients treated with natalizumab
Autoři
KOLČAVA, Jan (203 Česká republika, garant, domácí), Monika HULOVÁ (203 Česká republika, domácí), Lucie ŘÍHOVÁ (203 Česká republika), Josef BEDNAŘÍK (203 Česká republika, domácí) a Pavel ŠTOURAČ (203 Česká republika, domácí)
Vydání
NEUROLOGICAL SCIENCES, New York, Springer, 2021, 1590-1874
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30103 Neurosciences
Stát vydavatele
Itálie
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 3.830
Kód RIV
RIV/00216224:14110/21:00120838
Organizační jednotka
Lékařská fakulta
UT WoS
000590250900003
Klíčová slova anglicky
Natalizumab; Multiple sclerosis; T lymphocytes; Flow cytometry; JC virus
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 18. 2. 2022 13:40, Mgr. Tereza Miškechová
Anotace
V originále
Background Natalizumab is an effective therapy in the treatment of relapsing-remitting multiple sclerosis; it induces lymphocytosis (NIL, natalizumab-induced lymphocytosis) and changes the peripheral lymphocyte pattern. Methods This study aims to evaluate NIL, peripheral blood lymphocyte subsets, CD4/CD8 ratio, and their impacts on JCV index and clinical data-No Evidence of Disease Activity (NEDA-3) and annualized relapse rate (ARR) in patients treated with natalizumab. Results Forty-one patients (33 women) were included in the study. The mean duration of follow-up on natalizumab treatment was 6.7 +/- 3.2 years. Significant increases in relative lymphocytosis after 1 month, with a median of 40.4% (- 34.1 to + 145.5%) (p < 0.001), and after 1 year (49.0% (- 9.3 to + 127.6%)) (p < 0.001) were found. Significant differences were found after 1 month when comparing NIL between patients JCV-seroconverting (20.6% (- 17.7 to 72.7%)) and stable JCV-seronegative ones (43.5% (- 6.3 to +96.3%)) (p = 0.04). No significant difference NIL level was found between the patients exhibiting NEDA-3 status and those without it. ARR on natalizumab treatment correlated with CD4/CD8 ratio (r = 0.356; p = 0.021); patients who maintained NEDA-3 status over the whole treatment period exhibited a lower CD4/CD8 ratio (1.89 +/- 1.08 vs. 2.5 +/- 0.73; p < 0.04). Conclusion This contribution reports the CD4/CD8 ratio as a possible biomarker for better clinical efficacy of natalizumab in patients exhibiting a lower CD4/CD8 ratio. NIL did not correlate with long-term therapeutic efficacy in patients treated with natalizumab, but was demonstrated as lower in patients JCV-seroconverting in the course of follow-up.
Návaznosti
MUNI/A/1325/2019, interní kód MU |
| ||
MUNI/A/1600/2020, interní kód MU |
|