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B-cell repopulation dynamics and drug pharmacokinetics impact SARS-CoV-2 vaccine efficacy in anti-CD20-treated multiple sclerosis patients

Asplund Högelin, K. (författare)
Karolinska Institutet
Ruffin, N. (författare)
Karolinska Institutet
Pin, Elisa (författare)
KTH,Affinitets-proteomik,Science for Life Laboratory, SciLifeLab
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Hober, Sophia, Professor, 1965- (författare)
KTH,Science for Life Laboratory, SciLifeLab,Proteinteknologi
Nilsson, Peter (författare)
KTH,Science for Life Laboratory, SciLifeLab,Affinitets-proteomik
Starvaggi Cucuzza, C. (författare)
Karolinska Institutet
Khademi, M. (författare)
Karolinska Institutet
Olsson, T. (författare)
Karolinska Institutet
Piehl, F. (författare)
Al Nimer, F. (författare)
Karolinska Institutet
visa färre...
 (creator_code:org_t)
2022-07-20
2022
Engelska.
Ingår i: European Journal of Neurology. - : Wiley. - 1351-5101 .- 1468-1331. ; 29:11, s. 3317-3328
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background and purpose: Recent findings document a blunted humoral response to SARS-CoV-2 vaccination in patients on anti-CD20 treatment. Although most patients develop a cellular response, it is still important to identify predictors of seroconversion to optimize vaccine responses. Methods: We determined antibody responses after SARS-CoV-2 vaccination in a real-world cohort of multiple sclerosis patients (n = 94) treated with anti-CD20, mainly rituximab, with variable treatment duration (median = 2.9, range = 0.4–9.6 years) and time from last anti-CD20 infusion to vaccination (median = 190, range = 60–1032 days). Results: We find that presence of B cells and/or rituximab in blood predict seroconversion better than time since last infusion. Using multiple logistic regression, presence of >0.5% B cells increased probability of seroconversion with an odds ratio (OR) of 5.0 (95% confidence interval [CI] = 1.0–28.1, p = 0.055), whereas the corresponding OR for ≥6 months since last infusion was 1.45 (95% CI = 0.20–10.15, p = 0.705). In contrast, detectable rituximab levels were negatively associated with seroconversion (OR = 0.05, 95% CI = 0.002–0.392, p = 0.012). Furthermore, naïve and memory IgG+ B cells correlated with antibody levels. Although retreatment with rituximab at 4 weeks or more after booster depleted spike-specific B cells, it did not noticeably affect the rate of decline in antibody titers. Interferon-γ and/or interleukin-13 T-cell responses to the spike S1 domain were observed in most patients, but with no correlation to spike antibody levels. Conclusions: These findings are relevant for providing individualized guidance to patients and planning of vaccination schemes, in turn optimizing benefit–risk with anti-CD20. 

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

Nyckelord

B-cell depletion
multiple sclerosis
rituximab
SARS-CoV-2
vaccination
elasomeran
gamma interferon
interleukin 13
nucleocapsid protein
ocrelizumab
ofatumumab
SARS-CoV-2 vaccine
tozinameran
adult
antibody response
antibody titer
Article
B lymphocyte
cohort analysis
controlled study
demographics
female
human
human cell
immunophenotyping
limit of detection
major clinical study
male
pre B lymphocyte
retreatment
seroconversion
T lymphocyte subpopulation
treatment duration

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