MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1183/23120541.00418-2026

Медицинская библиотека · ERJ open research · 2026

Adjuvanted RSVPreF3 vaccine impact over three respiratory syncytial virus seasons in older adults with comorbidities.

Papi Alberto, Halpin David M G, Feldman Robert G, Ison Michael G, Schwarz Tino F, Lee Dong-Gun, Antonelli Incalzi Raffaele, Fissette Laurence, Xavier Stebin, David Marie-Pierre, Michaud Jean-Philippe, Kotb Shady, Maréchal Céline, Olivier Aurélie, Hulstrøm Veronica, Van der Wielen Marie

СтатьяПеревод в очереди

Аннотация

BACKGROUND

We explored the efficacy of AS01E-adjuvanted respiratory syncytial virus prefusion F protein-based vaccine (adjuvanted RSVPreF3) in subpopulations of participants with underlying medical conditions in the multi-country, phase 3 AReSVi-006 trial (conducted between May 2021 and May 2024).

METHODS

Medically stable ≥60-year-olds were 1:1-randomised to receive one adjuvanted RSVPreF3 or placebo dose pre-RSV season 1. In exploratory post hoc analyses in subgroups of participants with underlying conditions (including COPD, asthma, diabetes and obesity (body mass index ≥30 kg·m-2)), we evaluated efficacy of one vaccine dose against RSV-related lower respiratory tract disease (RSV-LRTD), RSV-related acute respiratory illness (RSV-ARI) and RSV-ARI-related complications (e.g., pneumonia, COPD/asthma exacerbation and cardiovascular events). We also evaluated (post hoc) RSV-ARI-related systemic corticosteroid and antibiotics use in participants with COPD or asthma.

RESULTS

The efficacy analyses comprised 12 468 vaccine and 12 498 placebo recipients. Efficacy against RSV-LRTD over three RSV seasons was similar among participants with COPD (75.1%, 95% CI: 40.2-91.4), asthma (65.8%, 31.0-84.7), diabetes (69.8%, 37.5-87.1) and obesity (74.1%, 56.4-85.5) as in the overall study population (62.9%, 97.5% CI: 46.7-74.8). Efficacy was also observed against RSV-ARI in these subgroups. Efficacy against RSV-ARI-related complications was 74.4% (95% CI: 11.2-95.2) in participants with COPD and 60.8% (-9.9-88.7) in those with asthma. Among participants with COPD, 15.4% (1.9-45.4) of RSV-ARI episodes in vaccine versus 22.4% (12.5-35.3) in placebo recipients were treated with systemic corticosteroids, and 46.2% (19.2-74.9) versus 56.9% (43.2-69.8) with antibiotics.

CONCLUSIONS

Post hoc analyses of the AReSVi-006 trial suggest that adjuvanted RSVPreF3 may help prevent RSV-ARI, RSV-LRTD and RSV-related complications in medically stable older adults with underlying medical conditions like COPD and asthma.

Для цитирования: Papi Alberto, Halpin David M G, Feldman Robert G, Ison Michael G, Schwarz Tino F, Lee Dong-Gun, Antonelli Incalzi Raffaele, Fissette Laurence, Xavier Stebin, David Marie-Pierre, Michaud Jean-Philippe, Kotb Shady, Maréchal Céline, Olivier Aurélie, Hulstrøm Veronica, Van der Wielen Marie. Adjuvanted RSVPreF3 vaccine impact over three respiratory syncytial virus seasons in older adults with comorbidities.. ERJ open research. 2026. DOI: 10.1183/23120541.00418-2026.
Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.