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Impact of siponimod on vaccination response in a randomized, placebo-controlled study
OBJECTIVE: To evaluate effects of siponimod on response to T-cell–dependent (influenza) and T-cell–independent (pneumococcal polysaccharide vaccine [PPV-23]) vaccinations in healthy participants. METHODS: In this double-blind, placebo-controlled, parallel-group study, each participant underwent a 7-...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608565/ https://www.ncbi.nlm.nih.gov/pubmed/28955715 http://dx.doi.org/10.1212/NXI.0000000000000398 |
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author | Ufer, Mike Shakeri-Nejad, Kasra Gardin, Anne Su, Zhenzhong Paule, Ines Marbury, Thomas C. Legangneux, Eric |
author_facet | Ufer, Mike Shakeri-Nejad, Kasra Gardin, Anne Su, Zhenzhong Paule, Ines Marbury, Thomas C. Legangneux, Eric |
author_sort | Ufer, Mike |
collection | PubMed |
description | OBJECTIVE: To evaluate effects of siponimod on response to T-cell–dependent (influenza) and T-cell–independent (pneumococcal polysaccharide vaccine [PPV-23]) vaccinations in healthy participants. METHODS: In this double-blind, placebo-controlled, parallel-group study, each participant underwent a 7-week treatment period and received intramuscular injections of influenza and PPV-23 vaccines (day 21). Participants were randomized to 4 treatment groups (N = 30 each) and received placebo or siponimod 2 mg once daily in concomitant, interrupted, or preceding fashion. Individual response to vaccination was defined by a ≥4-fold (influenza) antibody titer increase and by a ≥2-fold increase in serotype-specific immunoglobulin (Ig) G concentrations (PPV-23) on day 28 vs baseline. Responder rates were compared using noninferiority analysis. RESULTS: Mean influenza titers were similar to placebo in the preceding and interrupted groups but lower in the concomitant group. The proportion of participants with influenza titers ≥40 four weeks after vaccination (seroprotection) was similar to placebo across all groups and antigens. In each treatment group, response criteria were met for 3 of 4 antigens including H1N1 and H3N2. A noninferior response was determined in the context of preceding treatment but not interrupted or concomitant treatment. Regarding PPV-23, approximately 90%–100% of participants exhibited a ≥2-fold increase in IgG concentrations vs baseline. Noninferior responder rates were determined for each siponimod treatment group. CONCLUSIONS: Siponimod treatment had no relevant effect on antibody response to PPV-23. European Medicines Agency response criteria were essentially met for influenza, but titers were lower on concomitant treatment. Overall, these data suggest that siponimod has limited effect on the efficacy of vaccinations with neoantigens. CLASSIFICATION OF EVIDENCE: This study provides Class II evidence that in healthy persons, siponimod had limited effect on the immune response following influenza or pneumococcal vaccinations. |
format | Online Article Text |
id | pubmed-5608565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-56085652017-09-27 Impact of siponimod on vaccination response in a randomized, placebo-controlled study Ufer, Mike Shakeri-Nejad, Kasra Gardin, Anne Su, Zhenzhong Paule, Ines Marbury, Thomas C. Legangneux, Eric Neurol Neuroimmunol Neuroinflamm Article OBJECTIVE: To evaluate effects of siponimod on response to T-cell–dependent (influenza) and T-cell–independent (pneumococcal polysaccharide vaccine [PPV-23]) vaccinations in healthy participants. METHODS: In this double-blind, placebo-controlled, parallel-group study, each participant underwent a 7-week treatment period and received intramuscular injections of influenza and PPV-23 vaccines (day 21). Participants were randomized to 4 treatment groups (N = 30 each) and received placebo or siponimod 2 mg once daily in concomitant, interrupted, or preceding fashion. Individual response to vaccination was defined by a ≥4-fold (influenza) antibody titer increase and by a ≥2-fold increase in serotype-specific immunoglobulin (Ig) G concentrations (PPV-23) on day 28 vs baseline. Responder rates were compared using noninferiority analysis. RESULTS: Mean influenza titers were similar to placebo in the preceding and interrupted groups but lower in the concomitant group. The proportion of participants with influenza titers ≥40 four weeks after vaccination (seroprotection) was similar to placebo across all groups and antigens. In each treatment group, response criteria were met for 3 of 4 antigens including H1N1 and H3N2. A noninferior response was determined in the context of preceding treatment but not interrupted or concomitant treatment. Regarding PPV-23, approximately 90%–100% of participants exhibited a ≥2-fold increase in IgG concentrations vs baseline. Noninferior responder rates were determined for each siponimod treatment group. CONCLUSIONS: Siponimod treatment had no relevant effect on antibody response to PPV-23. European Medicines Agency response criteria were essentially met for influenza, but titers were lower on concomitant treatment. Overall, these data suggest that siponimod has limited effect on the efficacy of vaccinations with neoantigens. CLASSIFICATION OF EVIDENCE: This study provides Class II evidence that in healthy persons, siponimod had limited effect on the immune response following influenza or pneumococcal vaccinations. Lippincott Williams & Wilkins 2017-09-13 /pmc/articles/PMC5608565/ /pubmed/28955715 http://dx.doi.org/10.1212/NXI.0000000000000398 Text en Copyright © 2017 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Article Ufer, Mike Shakeri-Nejad, Kasra Gardin, Anne Su, Zhenzhong Paule, Ines Marbury, Thomas C. Legangneux, Eric Impact of siponimod on vaccination response in a randomized, placebo-controlled study |
title | Impact of siponimod on vaccination response in a randomized, placebo-controlled study |
title_full | Impact of siponimod on vaccination response in a randomized, placebo-controlled study |
title_fullStr | Impact of siponimod on vaccination response in a randomized, placebo-controlled study |
title_full_unstemmed | Impact of siponimod on vaccination response in a randomized, placebo-controlled study |
title_short | Impact of siponimod on vaccination response in a randomized, placebo-controlled study |
title_sort | impact of siponimod on vaccination response in a randomized, placebo-controlled study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5608565/ https://www.ncbi.nlm.nih.gov/pubmed/28955715 http://dx.doi.org/10.1212/NXI.0000000000000398 |
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