-
Je něco špatně v tomto záznamu ?
The impact of lymphocytosis and CD4/CD8 ratio on the anti-JCV antibody index and clinical data in patients treated with natalizumab
J. Kolcava, M. Hulova, L. Rihova, J. Bednarik, P. Stourac
Jazyk angličtina Země Itálie
Typ dokumentu časopisecké články
Grantová podpora
ref. - RVO (FNBr, 65269705)
Ministerstvo Zdravotnictví Ceské Republiky
MUNI / A / 1325/2019
Lékařská fakulta, Masarykova univerzita
NLK
ProQuest Central
od 2000-01-01 do Před 1 rokem
Medline Complete (EBSCOhost)
od 2000-02-01 do Před 1 rokem
Health & Medicine (ProQuest)
od 2000-01-01 do Před 1 rokem
Family Health Database (ProQuest)
od 2000-01-01 do Před 1 rokem
Psychology Database (ProQuest)
od 2000-01-01 do Před 1 rokem
- 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
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
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21025491
- 003
- CZ-PrNML
- 005
- 20211026133747.0
- 007
- ta
- 008
- 211013s2021 it f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s10072-020-04897-2 $2 doi
- 035 __
- $a (PubMed)33201361
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a it
- 100 1_
- $a Kolcava, Jan $u Faculty of Medicine, Masaryk University, Brno, Czech Republic $u Department of Neurology, University Hospital Brno, Jihlavská 340/20, 625 00, Brno, Czech Republic
- 245 14
- $a The impact of lymphocytosis and CD4/CD8 ratio on the anti-JCV antibody index and clinical data in patients treated with natalizumab / $c J. Kolcava, M. Hulova, L. Rihova, J. Bednarik, P. Stourac
- 520 9_
- $a 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.
- 650 _2
- $a CD8-pozitivní T-lymfocyty $7 D018414
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a imunologické faktory $x škodlivé účinky $7 D007155
- 650 12
- $a virus JC $7 D007577
- 650 12
- $a progresivní multifokální leukoencefalopatie $7 D007968
- 650 12
- $a lymfocytóza $x chemicky indukované $7 D008218
- 650 12
- $a roztroušená skleróza $7 D009103
- 650 12
- $a relabující-remitující roztroušená skleróza $x farmakoterapie $7 D020529
- 650 _2
- $a natalizumab $x škodlivé účinky $7 D000069442
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Hulova, Monika $u Faculty of Medicine, Masaryk University, Brno, Czech Republic $u Department of Neurology, University Hospital Brno, Jihlavská 340/20, 625 00, Brno, Czech Republic
- 700 1_
- $a Rihova, Lucie $u Department of Clinical Hematology, University Hospital Brno, Brno, Czech Republic
- 700 1_
- $a Bednarik, Josef $u Faculty of Medicine, Masaryk University, Brno, Czech Republic $u Department of Neurology, University Hospital Brno, Jihlavská 340/20, 625 00, Brno, Czech Republic
- 700 1_
- $a Stourac, Pavel $u Faculty of Medicine, Masaryk University, Brno, Czech Republic. Stourac.Pavel@fnbrno.cz $u Department of Neurology, University Hospital Brno, Jihlavská 340/20, 625 00, Brno, Czech Republic. Stourac.Pavel@fnbrno.cz
- 773 0_
- $w MED00005781 $t Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology $x 1590-3478 $g Roč. 42, č. 7 (2021), s. 2847-2853
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/33201361 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20211013 $b ABA008
- 991 __
- $a 20211026133753 $b ABA008
- 999 __
- $a ok $b bmc $g 1714516 $s 1145998
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2021 $b 42 $c 7 $d 2847-2853 $e 20201117 $i 1590-3478 $m Neurological sciences $n Neurol Sci $x MED00005781
- GRA __
- $a ref. - RVO (FNBr, 65269705) $p Ministerstvo Zdravotnictví Ceské Republiky
- GRA __
- $a MUNI / A / 1325/2019 $p Lékařská fakulta, Masarykova univerzita
- LZP __
- $a Pubmed-20211013