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DOI 10.1136/archdischild-2024-327040

Медицинская библиотека · Archives of disease in childhood · 2024

An open-label, phase IV randomised controlled trial of two schedules of a four-component meningococcal B vaccine in UK preterm infants.

Calvert Anna, Andrews Nick, Barlow Sheula, Borrow Ray, Black Charlotte, Bromage Barbara, Carr Jeremy, Clarke Paul, Collinson Andrew C, Few Karen, Hayward Naomi, Jones Christine E, Le Doare Kirsty, Ladhani Shamez N, Louth Jennifer, Papadopoulou Georgia, Pople Michelle, Scorrer Tim, Snape Matthew D, Heath Paul T

СтатьяРандомизированное исследованиеКлиническое исследование IV фазыМногоцентровое исследованиеПеревод в очереди

Аннотация

OBJECTIVE

To compare immunological responses of preterm infants to a four-component meningococcal B vaccine (4CMenB; Bexsero) following a 2+1 vs a 3+1 schedule, and to describe reactogenicity of routine vaccines.

DESIGN

An open-label, phase IV randomised study conducted across six UK sites.

SETTING

Neonatal units, postnatal wards, community recruitment following discharge.

PARTICIPANTS

129 preterm infants born at a gestation of <35 weeks (64 in group 1 (2+1), 65 in group 2 (3+1)) were included in the analysis. Analysis was completed for postprimary samples from 125 participants (59 in group 1, 66 in group 2) and for postbooster samples from 118 participants (59 in both groups).

INTERVENTIONS: Infants randomised to 4CMenB according to a 2+1 or a 3+1 schedule, alongside routine vaccines.

MAIN OUTCOME MEASURES: Serum bactericidal antibody (SBA) assays performed at 5, 12 and 13 months of age: geometric mean titres (GMTs) and proportions of infants achieving titres ≥4 compared between groups.

RESULTS

There were no significant differences in SBA GMTs between infants receiving a 2+1 compared with a 3+1 schedule following primary or booster vaccination, but a significantly higher proportion of infants had an SBA titre ≥4 against strain NZ98/254 (porin A) at 1 month after primary vaccination using a 3+1 compared with a 2+1 schedule (3+1: 87% (95% CI 76 to 94%), 2+1: 70% (95% CI 56 to 81%), p=0.03).At 12 weeks of age those in the 3+1 group, who received a dose of 4CMenB, had significantly more episodes of fever >38.0°C than those in the 2+1 group who did not (group 2+1: 2% (n=1); 3+1: 14% (n=9); p=0.02).

CONCLUSIONS

Both schedules were immunogenic in preterm infants, although a lower response against strain NZ98/254 was seen in the 2+1 schedule; ongoing disease surveillance is important in understanding the clinical significance of this difference.

TRIAL REGISTRATION NUMBER: NCT03125616.

Для цитирования: Calvert Anna, Andrews Nick, Barlow Sheula, Borrow Ray, Black Charlotte, Bromage Barbara, Carr Jeremy, Clarke Paul, Collinson Andrew C, Few Karen, Hayward Naomi, Jones Christine E, Le Doare Kirsty, Ladhani Shamez N, Louth Jennifer, Papadopoulou Georgia, Pople Michelle, Scorrer Tim, Snape Matthew D, Heath Paul T. An open-label, phase IV randomised controlled trial of two schedules of a four-component meningococcal B vaccine in UK preterm infants.. Archives of disease in childhood. 2024. DOI: 10.1136/archdischild-2024-327040.

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