Long-term immunogenicity and safety of a non-typeable Haemophilus influenzae-Moraxella catarrhalis vaccine : 4-year follow-up of a phase 1 multicentre trial
A multicomponent vaccine has been developed to reduce the frequency of acute exacerbations of COPD associated with non-typeable Haemophilus influenzae (NTHi) and Moraxella catarrhalis (Mcat) infections, containing NTHi (PD and PE-PilA) and Mcat (UspA2) surface proteins. In a randomised, observer-bli...
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creator | De Smedt, Philippe Leroux-Roels, Geert Vandermeulen, Corinne Tasciotti, Annaelisa Di Maro, Gennaro Dozot, Marie Casula, Daniela Annaratone, Margherita Riccucci, Daniele Arora, Ashwani Kumar |
description | A multicomponent vaccine has been developed to reduce the frequency of acute exacerbations of COPD associated with non-typeable Haemophilus influenzae (NTHi) and Moraxella catarrhalis (Mcat) infections, containing NTHi (PD and PE-PilA) and Mcat (UspA2) surface proteins. In a randomised, observer-blind, placebo-controlled study with two steps (NCT02547974), the investigational vaccine had good immunogenicity and no safety concerns were identified. In step 2, 90 adults aged 50-71 years with smoking history received two doses 60 days apart of one of two AS01(E)-adjuvanted formulations containing 10 mg of each antigen (10-10-AS01) or 10 mu g NTHi antigens and 3.3 mu g UspA2 (10-3-AS01), or placebo. Long-term persistence of antigen-specific humoral antibodies was assessed in 81 participants during 3 years of follow-up after the initial 14-month study (NCT03201211).
Antigen-specific antibody concentrations were measured in blood samples taken every 6 months. Safety monitoring evaluated serious adverse events (SAEs) and potential immune-mediated disease (pIMD).
Immune responses against NTHi antigens persisted up to 4 years post-vaccination. For PD, PE and PilA, at each follow-up time point, adjusted antibody geometric mean concentrations (GMCs) were higher (non-overlapping 95% confidence intervals [CIs]) in the vaccine groups versus placebo and versus prevaccination. Antibody GMC point estimates were higher with 10-3-AS01 than with 10-10-AS01. For UspA2, 95% CIs included 1 for GMC ratios of 10-10-AS01 or 10-3-AS01 to placebo at each time point. During follow-up, SAEs were reported in nine (11.1%) participants, one of which was fatal (lung cancer, 607 days after second 10-10-AS01 dose). One non-serious pIMD, trigeminal neuralgia, was reported 771 days after second 10-3-AS01 dose. The SAEs and pIMD were considered not related to vaccination.
Immune responses against NTHi antigens persisted for 4 years after two-dose vaccination with the investigational NTHi-Mcat vaccine. There was no persistent response against the Mcat antigen. No safety concerns were identified during the long-term follow-up. (C) 2021 GlaxoSmithKline Biologicals S.A. Published by Elsevier Ltd. |
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Antigen-specific antibody concentrations were measured in blood samples taken every 6 months. Safety monitoring evaluated serious adverse events (SAEs) and potential immune-mediated disease (pIMD).
Immune responses against NTHi antigens persisted up to 4 years post-vaccination. For PD, PE and PilA, at each follow-up time point, adjusted antibody geometric mean concentrations (GMCs) were higher (non-overlapping 95% confidence intervals [CIs]) in the vaccine groups versus placebo and versus prevaccination. Antibody GMC point estimates were higher with 10-3-AS01 than with 10-10-AS01. For UspA2, 95% CIs included 1 for GMC ratios of 10-10-AS01 or 10-3-AS01 to placebo at each time point. During follow-up, SAEs were reported in nine (11.1%) participants, one of which was fatal (lung cancer, 607 days after second 10-10-AS01 dose). One non-serious pIMD, trigeminal neuralgia, was reported 771 days after second 10-3-AS01 dose. The SAEs and pIMD were considered not related to vaccination.
Immune responses against NTHi antigens persisted for 4 years after two-dose vaccination with the investigational NTHi-Mcat vaccine. There was no persistent response against the Mcat antigen. No safety concerns were identified during the long-term follow-up. (C) 2021 GlaxoSmithKline Biologicals S.A. Published by Elsevier Ltd.</description><identifier>ISSN: 2590-1362</identifier><identifier>EISSN: 2590-1362</identifier><language>eng</language><subject>Acute exacerbation ; Antibody persistence ; ANTIGEN ; CHALLENGES ; Clinical trial ; COPD ; DOMAIN ; EXACERBATIONS ; Haemophilus influenzae ; Medicine and Health Sciences ; MICROBIOME ; Moraxella catarrhalis ; PROTEIN VACCINE ; STREPTOCOCCUS-PNEUMONIAE ; SURVIVAL ; VITRONECTIN</subject><creationdate>2021</creationdate><rights>Creative Commons Attribution 4.0 International Public License (CC-BY 4.0) info:eu-repo/semantics/openAccess</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,315,780,784,4023,27859</link.rule.ids></links><search><creatorcontrib>De Smedt, Philippe</creatorcontrib><creatorcontrib>Leroux-Roels, Geert</creatorcontrib><creatorcontrib>Vandermeulen, Corinne</creatorcontrib><creatorcontrib>Tasciotti, Annaelisa</creatorcontrib><creatorcontrib>Di Maro, Gennaro</creatorcontrib><creatorcontrib>Dozot, Marie</creatorcontrib><creatorcontrib>Casula, Daniela</creatorcontrib><creatorcontrib>Annaratone, Margherita</creatorcontrib><creatorcontrib>Riccucci, Daniele</creatorcontrib><creatorcontrib>Arora, Ashwani Kumar</creatorcontrib><title>Long-term immunogenicity and safety of a non-typeable Haemophilus influenzae-Moraxella catarrhalis vaccine : 4-year follow-up of a phase 1 multicentre trial</title><description>A multicomponent vaccine has been developed to reduce the frequency of acute exacerbations of COPD associated with non-typeable Haemophilus influenzae (NTHi) and Moraxella catarrhalis (Mcat) infections, containing NTHi (PD and PE-PilA) and Mcat (UspA2) surface proteins. In a randomised, observer-blind, placebo-controlled study with two steps (NCT02547974), the investigational vaccine had good immunogenicity and no safety concerns were identified. In step 2, 90 adults aged 50-71 years with smoking history received two doses 60 days apart of one of two AS01(E)-adjuvanted formulations containing 10 mg of each antigen (10-10-AS01) or 10 mu g NTHi antigens and 3.3 mu g UspA2 (10-3-AS01), or placebo. Long-term persistence of antigen-specific humoral antibodies was assessed in 81 participants during 3 years of follow-up after the initial 14-month study (NCT03201211).
Antigen-specific antibody concentrations were measured in blood samples taken every 6 months. Safety monitoring evaluated serious adverse events (SAEs) and potential immune-mediated disease (pIMD).
Immune responses against NTHi antigens persisted up to 4 years post-vaccination. For PD, PE and PilA, at each follow-up time point, adjusted antibody geometric mean concentrations (GMCs) were higher (non-overlapping 95% confidence intervals [CIs]) in the vaccine groups versus placebo and versus prevaccination. Antibody GMC point estimates were higher with 10-3-AS01 than with 10-10-AS01. For UspA2, 95% CIs included 1 for GMC ratios of 10-10-AS01 or 10-3-AS01 to placebo at each time point. During follow-up, SAEs were reported in nine (11.1%) participants, one of which was fatal (lung cancer, 607 days after second 10-10-AS01 dose). One non-serious pIMD, trigeminal neuralgia, was reported 771 days after second 10-3-AS01 dose. The SAEs and pIMD were considered not related to vaccination.
Immune responses against NTHi antigens persisted for 4 years after two-dose vaccination with the investigational NTHi-Mcat vaccine. There was no persistent response against the Mcat antigen. No safety concerns were identified during the long-term follow-up. (C) 2021 GlaxoSmithKline Biologicals S.A. Published by Elsevier Ltd.</description><subject>Acute exacerbation</subject><subject>Antibody persistence</subject><subject>ANTIGEN</subject><subject>CHALLENGES</subject><subject>Clinical trial</subject><subject>COPD</subject><subject>DOMAIN</subject><subject>EXACERBATIONS</subject><subject>Haemophilus influenzae</subject><subject>Medicine and Health Sciences</subject><subject>MICROBIOME</subject><subject>Moraxella catarrhalis</subject><subject>PROTEIN VACCINE</subject><subject>STREPTOCOCCUS-PNEUMONIAE</subject><subject>SURVIVAL</subject><subject>VITRONECTIN</subject><issn>2590-1362</issn><issn>2590-1362</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>ADGLB</sourceid><recordid>eNqtjUtKxEAURYMo2Gjv4W2gIJ_-RIcJsYPorDHOwkv5kpS8VIWqSmtci4s1ogMX4OgeuJdzz4JVvL0JRZTs4vM_fBmsnXsNwzCO0ijdbVbB54PRnfBkB1DDMGnTkVZS-RlQv4DDlhY0LSBoo4WfR8KGCUqkwYy94smB0i1PpD-QxKOx-E7MCBI9WtsjKwcnlFJpglvYiJnQQmuYzZuYxh_z2KMjiGCY2CtJ2lsCbxXydXDRIjta_-ZVUNwVx7wUXb-salaNpeWoNqhqtLJXJ6qn7rtqqA6jsqjyLDuUz0me76tDFj9V-2R7nyb_5fkCDcJ0fw</recordid><startdate>2021</startdate><enddate>2021</enddate><creator>De Smedt, Philippe</creator><creator>Leroux-Roels, Geert</creator><creator>Vandermeulen, Corinne</creator><creator>Tasciotti, Annaelisa</creator><creator>Di Maro, Gennaro</creator><creator>Dozot, Marie</creator><creator>Casula, Daniela</creator><creator>Annaratone, Margherita</creator><creator>Riccucci, Daniele</creator><creator>Arora, Ashwani Kumar</creator><scope>ADGLB</scope></search><sort><creationdate>2021</creationdate><title>Long-term immunogenicity and safety of a non-typeable Haemophilus influenzae-Moraxella catarrhalis vaccine : 4-year follow-up of a phase 1 multicentre trial</title><author>De Smedt, Philippe ; Leroux-Roels, Geert ; Vandermeulen, Corinne ; Tasciotti, Annaelisa ; Di Maro, Gennaro ; Dozot, Marie ; Casula, Daniela ; Annaratone, Margherita ; Riccucci, Daniele ; Arora, Ashwani Kumar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-ghent_librecat_oai_archive_ugent_be_01HEWCBBGHX3CC7WGB2VW735J83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acute exacerbation</topic><topic>Antibody persistence</topic><topic>ANTIGEN</topic><topic>CHALLENGES</topic><topic>Clinical trial</topic><topic>COPD</topic><topic>DOMAIN</topic><topic>EXACERBATIONS</topic><topic>Haemophilus influenzae</topic><topic>Medicine and Health Sciences</topic><topic>MICROBIOME</topic><topic>Moraxella catarrhalis</topic><topic>PROTEIN VACCINE</topic><topic>STREPTOCOCCUS-PNEUMONIAE</topic><topic>SURVIVAL</topic><topic>VITRONECTIN</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>De Smedt, Philippe</creatorcontrib><creatorcontrib>Leroux-Roels, Geert</creatorcontrib><creatorcontrib>Vandermeulen, Corinne</creatorcontrib><creatorcontrib>Tasciotti, Annaelisa</creatorcontrib><creatorcontrib>Di Maro, Gennaro</creatorcontrib><creatorcontrib>Dozot, Marie</creatorcontrib><creatorcontrib>Casula, Daniela</creatorcontrib><creatorcontrib>Annaratone, Margherita</creatorcontrib><creatorcontrib>Riccucci, Daniele</creatorcontrib><creatorcontrib>Arora, Ashwani Kumar</creatorcontrib><collection>Ghent University Academic Bibliography</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>De Smedt, Philippe</au><au>Leroux-Roels, Geert</au><au>Vandermeulen, Corinne</au><au>Tasciotti, Annaelisa</au><au>Di Maro, Gennaro</au><au>Dozot, Marie</au><au>Casula, Daniela</au><au>Annaratone, Margherita</au><au>Riccucci, Daniele</au><au>Arora, Ashwani Kumar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-term immunogenicity and safety of a non-typeable Haemophilus influenzae-Moraxella catarrhalis vaccine : 4-year follow-up of a phase 1 multicentre trial</atitle><date>2021</date><risdate>2021</risdate><issn>2590-1362</issn><eissn>2590-1362</eissn><abstract>A multicomponent vaccine has been developed to reduce the frequency of acute exacerbations of COPD associated with non-typeable Haemophilus influenzae (NTHi) and Moraxella catarrhalis (Mcat) infections, containing NTHi (PD and PE-PilA) and Mcat (UspA2) surface proteins. In a randomised, observer-blind, placebo-controlled study with two steps (NCT02547974), the investigational vaccine had good immunogenicity and no safety concerns were identified. In step 2, 90 adults aged 50-71 years with smoking history received two doses 60 days apart of one of two AS01(E)-adjuvanted formulations containing 10 mg of each antigen (10-10-AS01) or 10 mu g NTHi antigens and 3.3 mu g UspA2 (10-3-AS01), or placebo. Long-term persistence of antigen-specific humoral antibodies was assessed in 81 participants during 3 years of follow-up after the initial 14-month study (NCT03201211).
Antigen-specific antibody concentrations were measured in blood samples taken every 6 months. Safety monitoring evaluated serious adverse events (SAEs) and potential immune-mediated disease (pIMD).
Immune responses against NTHi antigens persisted up to 4 years post-vaccination. For PD, PE and PilA, at each follow-up time point, adjusted antibody geometric mean concentrations (GMCs) were higher (non-overlapping 95% confidence intervals [CIs]) in the vaccine groups versus placebo and versus prevaccination. Antibody GMC point estimates were higher with 10-3-AS01 than with 10-10-AS01. For UspA2, 95% CIs included 1 for GMC ratios of 10-10-AS01 or 10-3-AS01 to placebo at each time point. During follow-up, SAEs were reported in nine (11.1%) participants, one of which was fatal (lung cancer, 607 days after second 10-10-AS01 dose). One non-serious pIMD, trigeminal neuralgia, was reported 771 days after second 10-3-AS01 dose. The SAEs and pIMD were considered not related to vaccination.
Immune responses against NTHi antigens persisted for 4 years after two-dose vaccination with the investigational NTHi-Mcat vaccine. There was no persistent response against the Mcat antigen. No safety concerns were identified during the long-term follow-up. (C) 2021 GlaxoSmithKline Biologicals S.A. Published by Elsevier Ltd.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | Acute exacerbation Antibody persistence ANTIGEN CHALLENGES Clinical trial COPD DOMAIN EXACERBATIONS Haemophilus influenzae Medicine and Health Sciences MICROBIOME Moraxella catarrhalis PROTEIN VACCINE STREPTOCOCCUS-PNEUMONIAE SURVIVAL VITRONECTIN |
title | Long-term immunogenicity and safety of a non-typeable Haemophilus influenzae-Moraxella catarrhalis vaccine : 4-year follow-up of a phase 1 multicentre trial |
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