Long-term immunogenicity and safety of a non-typeable Haemophilus influenzae-Moraxella catarrhalis vaccine: 4-year follow-up of a phase 1 multicentre trial

被引:8
作者
De Smedt, Philippe [1 ]
Leroux-Roels, Geert [2 ,3 ]
Vandermeulen, Corinne [4 ]
Tasciotti, Annaelisa [5 ]
Di Maro, Gennaro [5 ]
Dozot, Marie [6 ]
Casula, Daniela [5 ]
Annaratone, Margherita [5 ]
Riccucci, Daniele [5 ]
Arora, Ashwani Kumar [5 ]
机构
[1] Univ Antwerp, Ctr Evaluat Vaccinat, Vaccine & Infect Dis Inst, Antwerp, Belgium
[2] Univ Ghent, Ctr Vaccinol, Ghent, Belgium
[3] Ghent Univ Hosp, Ghent, Belgium
[4] Leuven Univ, Dept Publ Hlth & Primary Care, KU Leuven, Vaccinol Ctr, Leuven, Belgium
[5] GSK, Siena, Italy
[6] GSK, Rixensart, Belgium
关键词
Acute exacerbation; Antibody persistence; Clinical trial; COPD; Haemophilus influenzae; Moraxella catarrhalis; STREPTOCOCCUS-PNEUMONIAE; PROTEIN VACCINE; VITRONECTIN; COPD; EXACERBATIONS; MICROBIOME; CHALLENGES; SURVIVAL; DISEASE; ANTIGEN;
D O I
10.1016/j.jvacx.2021.100124
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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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页数:7
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