Introduction: Presence of anti-JC-virus antibodies (JCVAbs) is associated with the increased risk of natalizumab (NAT)-related progressive multifocal leukoencephalopathy (PML). Little is known about seroconversion rate and time to seroconversion in relapsing-remitting multiple sclerosis (RRMS) patients treated with NAT in Poland. The aim of the study was to assess the true risk of PML, seroconversion rate, and time to seroconversion in all JCVAb-negative RRMS patients treated with NAT in Poland. Methods: Demographic and clinical data of all Polish RRMS patients treated with NAT reimbursed by National Health Fund (NFZ) were prospectively collected in electronic files using the Therapeutic Programme Monitoring System provided by NFZ. The assessment of JCVAb presence (without collection of JCVAb index value) in serum (Unilabs, STRATIFY JCV: anti-JCV antibody ELISA) was done at the beginning of therapy and then repeated every 6 months. The maximum follow-up time was 4 years. In Poland, since 2013, according to the NFZ drug program guidance, only patients with negative JCVAb test have started treatment with NAT. Results: In all Polish multiple sclerosis centers, 210 negative JCVAb RRMS patients with at least 9 (±3) months of observation (146 females, 64 males, and the median age at baseline: 33 years) were included in the study. During the follow-up period, JCVAb status changed from negative to positive in 34 patients (16.2%). For half of the patients, the seroconversion was diagnosed 1 year after starting NAT treatment. In 4 patients (1.9%) during follow-up, JCVAb status changed again from positive to negative. In Poland, before establishment of NFZ drug program, 4 cases of PML in patients treated with NAT in clinical trials were diagnosed. In the NFZ drug program, since 2013, no patient treated with NAT has been diagnosed with PML. Conclusions: NAT therapy in JCV-seronegative RRMS patients is safe and results in the absence of PML cases. In Poland, JCV seroconversion rate is similar to that observed in other European countries.

1.
Browne
P
,
Chandraratna
D
,
Angood
C
,
Tremlett
H
,
Baker
C
,
Taylor
BV
,
.
Atlas of multiple sclerosis 2013: a growing global problem with widespread inequity
.
Neurology
.
2014
;
83
(
11
):
1022
4
.
2.
Singer
BA
.
The role of natalizumab in the treatment of multiple sclerosis: benefits and risks
.
Ther Adv Neurol Disord
.
2017
;
10
(
9
):
327
36
.
3.
Major
EO
,
Yousry
TA
,
Clifford
DB
.
Pathogenesis of progressive multifocal leukoencephalopathy and risks associated withtreatments for multiple sclerosis: a decade of lessons learned
.
Lancet Neurol
.
2018
;
175
:
467
80
.
4.
Biogen
.
TYSABRI® (natalizumab): PML incidence in patients receiving TYSABRI
.
2016
.
5.
Vennegoor
A
,
van Rossum
JA
,
Leurs
C
,
Wattjes
MP
,
Rispens
T
,
Murk
JL
,
.
High cumulative JC virus seroconversion rate during long-term use of natalizumab
.
Eur J Neurol
.
2016
;
23
(
6
):
1079
85
.
6.
Azimi
A
,
Hanaei
S
,
Sahraian
MA
,
Mohammadifar
M
,
Ramagopalan
SV
,
Ghajarzadeh
M
.
Incidence of seroconversion and sero-reversion in patients with multiple sclerosis (MS) who had been treated with natalizumab: a systematic review and meta-analysis
.
J Clin Neurosci
.
2020
;
71
:
129
34
.
7.
Kapica-Topczewska
K
,
Brola
W
,
Fudala
M
,
Tarasiuk
J
,
Chorazy
M
,
Snarska
K
,
.
Prevalence of multiple sclerosis in Poland
.
Mult Scler Relat Disord
.
2018
;
21
:
51
5
.
8.
Kapica-Topczewska
K
,
Collin
F
,
Tarasiuk
J
,
Chorąży
M
,
Czarnowska
A
,
Kwaśniewski
M
,
.
Clinical and epidemiological characteristics of multiple sclerosis patients receiving disease-modifying treatment in Poland
.
Neurol Neurochir Pol
.
2020
;
54
(
2
):
161
8
.
9.
Baldwin
KJ
,
Hogg
JP
.
Progressive multifocal leukoencephalopathy in patients with multiple sclerosis
.
Curr Opin Neurol
.
2013
;
26
(
3
):
318
23
.
10.
Correia
I
,
Jesus-Ribeiro
J
,
Batista
S
,
Martins
AI
,
Nunes
C
,
Macário
MC
,
.
Anti-JCV antibody serostatus and longitudinal evaluation in a Portuguese multiple sclerosis population
.
J Clin Neurosci
.
2017
;
45
:
257
60
.
11.
Gagne Brosseau
MS
,
Stobbe
G
,
Wundes
A
.
Natalizumab-related PML 2 weeks after negative anti-JCV antibody assay
.
Neurology
.
2016
;
86
(
5
):
484
6
.
12.
Viscidi
RP
,
Khanna
N
,
Tan
CS
,
Li
X
,
Jacobson
L
,
Clifford
DB
,
.
JC virus antibody and viremia as predictors of progressive multifocal leukoencephalopathy in human immunodeficiency virus-1-infected individuals
.
Clin Infect Dis
.
2011
;
53
(
7
):
711
5
.
13.
Paz
SPC
,
Branco
L
,
Pereira
MAC
,
Spessotto
C
,
Fragoso
YD
.
Systematic review of the published data on the worldwide prevalence of John Cunningham virus in patients with multiple sclerosis and neuromyelitis optica
.
Epidemiol Health
.
2018
;
40
:
e2018001
.
14.
Bellizzi
A
,
Anzivino
E
,
Rodio
DM
,
Palamara
AT
,
Nencioni
L
,
Pietropaolo
V
.
New insights on human polyomavirus JC and pathogenesis of progressive multifocal leukoencephalopathy
.
Clin Dev Immunol
.
2013
;
2013
:
839719
.
15.
Schwab
N
,
Schneider-Hohendorf
T
,
Hoyt
T
,
Gross
CC
,
Meuth
SG
,
Klotz
L
,
.
Anti-JCV serology during natalizumab treatment: review and meta-analysis of 17 independent patient cohorts analyzing anti-John Cunningham polyoma virus sero-conversion rates under natalizumab treatment and differences between technical and biological sero-converters
.
Mult Scler
.
2017
;
245
:
1352458517728814–73
.
16.
Auer
M
,
Hegen
H
,
Sellner
J
,
Oppermann
K
,
Bsteh
G
,
Di Pauli
F
,
.
Conversion and reversion of anti-John Cunningham virus antibody serostatus: a prospective study
.
Brain Behav
.
2019
;
9
(
7
):
e01332
.
17.
Plavina
T
,
Subramanyam
M
,
Bloomgren
G
,
Richman
S
,
Pace
A
,
Lee
S
,
.
Anti-JC virus antibody levels in serum or plasma further define risk of natalizumab-associated progressive multifocal leukoencephalopathy
.
Ann Neurol
.
2014
;
76
(
6
):
802
12
.
18.
Lanza Cariccio
V
,
Bramanti
P
,
Mazzon
E
.
Biomarkers identification for PML monitoring, during natalizumab (Tysabri®) treatment in relapsing-remitting multiple sclerosis
.
Mult Scler Relat Disord
.
2018
;
20
:
93
9
.
19.
Kolcava
J
,
Hulova
M
,
Benesova
Y
,
Bednarik
J
,
Stourac
P
.
The value of anti-JCV antibody index assessment in multiple sclerosis patients treated with natalizumab with respect to demographic, clinical and radiological findings
.
Mult Scler Relat Disord
.
2019
;
30
:
187
91
.
20.
Alroughani
R
,
Akhtar
S
,
Ahmed
SF
,
Khoury
SJ
,
Al-Hashel
JY
,
Sahraian
MA
,
.
JC virus seroprevalence and seroconversion in multiple sclerosis cohort: a Middle-Eastern study
.
J Neurol Sci
.
2016
;
360
:
61
5
.
21.
Outteryck
O
,
Zéphir
H
,
Salleron
J
,
Ongagna
JC
,
Etxeberria
A
,
Collongues
N
,
.
JC-virus seroconversion in multiple sclerosis patients receiving natalizumab
.
Mult Scler
.
2014
;
20
(
7
):
822
9
.
22.
Arndt
N
,
Reder
AT
,
Javed
A
.
Variability of John Cunningham virus (JCV) index in multiple sclerosis patients treated with natalizumab in routine clinical practice
.
Mult Scler
.
2015
;
21
:
654
79
.
23.
Schwab
N
,
Schneider-Hohendorf
T
,
Pignolet
B
,
Breuer
J
,
Gross
CC
,
Göbel
K
,
.
Therapy with natalizumab is associated with high JCV seroconversion and rising JCV index values
.
Neurol Neuroimmunol Neuroinflamm
.
2016
;
3
(
1
):
e195
.
24.
Raffel
J
,
Gafson
AR
,
Malik
O
,
Nicholas
R
.
Anti-JC virus antibody titres increase over time with natalizumab treatment
.
Mult Scler
.
2015
;
21
(
14
):
1833
8
.
25.
Chen
Y
,
Bord
E
,
Tompkins
T
,
Miller
J
,
Tan
CS
,
Kinkel
RP
,
.
Asymptomatic reactivation of JC virus in patients treated with natalizumab
.
N Engl J Med
.
2009
;
361
(
11
):
1067
74
.
26.
Schwab
N
,
Schneider-Hohendorf
T
,
Melzer
N
,
Cutter
G
,
Wiendl
H
.
Natalizumab-associated PML: challenges with incidence, resulting risk, and riskstratification
.
Neurology
.
2017
;
88
:
1197
205
.
You do not currently have access to this content.