The impact of lymphocytosis and CD4/CD8 ratio on the anti-JCV antibody index and clinical data in patients treated with natalizumab
Jazyk angličtina Země Itálie Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
ref. - RVO (FNBr, 65269705)
Ministerstvo Zdravotnictví Ceské Republiky
MUNI / A / 1325/2019
Lékařská fakulta, Masarykova univerzita
PubMed
33201361
DOI
10.1007/s10072-020-04897-2
PII: 10.1007/s10072-020-04897-2
Knihovny.cz E-zdroje
- Klíčová slova
- Flow cytometry, JC virus, Multiple sclerosis, Natalizumab, T lymphocytes,
- MeSH
- CD8-pozitivní T-lymfocyty MeSH
- imunologické faktory škodlivé účinky MeSH
- lidé MeSH
- lymfocytóza * chemicky indukované MeSH
- natalizumab škodlivé účinky MeSH
- progresivní multifokální leukoencefalopatie * MeSH
- relabující-remitující roztroušená skleróza * farmakoterapie MeSH
- roztroušená skleróza * MeSH
- virus JC * MeSH
- Check Tag
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- imunologické faktory MeSH
- natalizumab MeSH
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.
Department of Clinical Hematology University Hospital Brno Brno Czech Republic
Department of Neurology University Hospital Brno Jihlavská 340 20 625 00 Brno Czech Republic
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