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Clinical Trial
. 2013 Aug 6;81(6):552-8.
doi: 10.1212/WNL.0b013e31829e6fbf. Epub 2013 Jul 12.

Teriflunomide effect on immune response to influenza vaccine in patients with multiple sclerosis

Affiliations
Clinical Trial

Teriflunomide effect on immune response to influenza vaccine in patients with multiple sclerosis

Amit Bar-Or et al. Neurology. .

Abstract

Objective: To investigate the effect of teriflunomide on the efficacy and safety of seasonal influenza vaccine.

Methods: The 2011/2012 seasonal influenza vaccine (containing H1N1, H3N2, and B strains) was administered to patients with relapsing forms of multiple sclerosis (RMS) treated for ≥6 months with teriflunomide 7 mg (n = 41) or 14 mg (n = 41), or interferon-β-1 (IFN-β-1; n = 46). The primary endpoint was the proportion of patients with influenza strain-specific antibody titers ≥40, 28 days postvaccination.

Results: More than 90% of patients achieved postvaccination antibody titers ≥40 for H1N1 and B in all groups. For H3N2, titers ≥40 were achieved in ≥90% of patients in the 7 mg and IFN-β-1 groups, and in 77% of the 14-mg group, respectively. A high proportion of patients already had detectable antibodies for each influenza strain at baseline. Geometric mean titer ratios (post/prevaccination) were ≥2.5 for all groups and strains, except for H1N1 in the 14-mg group (2.3). The proportion of patients with a prevaccination titer <40 achieving seroprotection was ≥61% across the 3 treatment groups and 3 influenza strains. However, fewer patients in the 14-mg than the 7-mg or IFN-β-1 groups exhibited seroprotection to H3N2 (61% vs. 78% and 82%, respectively).

Conclusion: Teriflunomide-treated patients generally mounted effective immune responses to seasonal influenza vaccination, consistent with preservation of protective immune responses.

Classification of evidence: This study provides Class II evidence that teriflunomide generally does not adversely impact the ability of patients with RMS to mount immune responses to influenza vaccination.

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Figures

Figure 1
Figure 1. Proportion of patients with influenza antibody titers ≥40 at 28 days postvaccination (per-protocol population)
European criteria for efficacy of influenza vaccination in an 18- to 60-year-old population require achievement of a hemagglutination inhibition titer ≥40 by 70% of patients, as indicated by the dashed line. IFN = interferon.

References

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