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HBV and VZV seroprotection loss in MS patients under DMT.

Authors :
Ladeira F
Oliveira T
Soares M
Araujo C
Sousa A
Brum M
Sequeira J
Capela C
Source :
Multiple sclerosis and related disorders [Mult Scler Relat Disord] 2023 Feb; Vol. 70, pp. 104490. Date of Electronic Publication: 2022 Dec 28.
Publication Year :
2023

Abstract

Background: Strategies recommended to decrease the risk of infection associated with the use of multiple sclerosis disease-modifying treatments include screening and immunization against common viral infections such as varicella-zoster (VZV) and hepatitis B (HBV). However, the data concerning the durability of those vaccine responses and the need for re-test is scarce.<br />Objectives: We aimed to evaluate HBV and VZV seroprotection loss in MS patients under DMT.<br />Methods: We conducted a cohort study including patients with basal seroprotective titers against HBV/VZV viruses and a subsequent serology performed at least 3 months apart. We evaluated predictors of seroprotection loss through a binary regression.<br />Results: HBV seroprotection loss occurred in one-fifth of patients in a median interval of 21.3 months. Anti-CD20 treatment (OR 8.559 95%CI 3.467- 21.130, p < 000.1), age at last serology higher or equal to 55 years (OR 7.506, 95% CI 2.473-22.786, p < 0.001) and basal HBsAb titer (OR 0.992, 95%CI 0.987 -0.996, p=0.001) increase the risk of seroprotection loss. VZV seroprotection loss occurred rarely in a median interval of 21.3 months. We could not identify any factor associated with an increased risk of VZV seroprotection loss.<br />Conclusions: Anti-CD20 drugs are associated with a loss of seroprotection against HBV in a short-interval follow-up.<br />Competing Interests: Declaration of Competing Interest The authors report no conflicts of interest.<br /> (Copyright © 2022 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
2211-0356
Volume :
70
Database :
MEDLINE
Journal :
Multiple sclerosis and related disorders
Publication Type :
Academic Journal
Accession number :
36621160
Full Text :
https://doi.org/10.1016/j.msard.2022.104490