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在英格兰,ChAdOx1-S COVID-19 加强疫苗接种对奥密克戎和德尔塔变异株的有效性。

Effectiveness of ChAdOx1-S COVID-19 booster vaccination against the Omicron and Delta variants in England.

机构信息

UK Health Security Agency, London, UK.

NIHR Health Protection Research Unit in Vaccines and Immunisation, London School of Hygiene and Tropical Medicine, London, UK.

出版信息

Nat Commun. 2022 Dec 12;13(1):7688. doi: 10.1038/s41467-022-35168-7.

DOI:10.1038/s41467-022-35168-7
PMID:36509743
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9744366/
Abstract

Despite the availability of the ChAdOx1-S booster vaccine, little is known about the real-world effectiveness although clinical trials have demonstrated enhanced immunity following a ChAdOx1-S booster. In England 43,171 individuals received a ChAdOx1-S booster whilst 13,038,908 individuals received BNT162b2 in the same period. ChAdOx1-S booster recipients were more likely to be female (adjusted odds ratio (OR) 1.67 (1.64-1.71)), in a clinical risk group (adjusted OR 1.58 (1.54-1.63)), in the clinically extremely vulnerable group (adjusted OR 1.84 (1.79-1.89)) or severely immunosuppressed (adjusted OR 2.05 (1.96-2.13)). The effectiveness of the ChAdOx1-S and BNT162b2 boosters is estimated here using a test-negative case-control study. Protection against symptomatic disease with the Omicron variant peaks at 66.1% (16.6 to 86.3%) and 68.5% (65.7 to 71.2%) for the ChAdOx1-S and BNT162b2 boosters in older adults. Protection against hospitalisation peaks at 82.3% (64.2 to 91.3%) and 90.9% (88.7 to 92.7%). For Delta, effectiveness against hospitalisation is 80.9% (15.6% to 95.7%) and 93.9% (92.8% to 94.9%) after ChAdOx1-S and BNT162b2 booster vaccination. This study supports the consideration of ChAdOx1-S booster vaccination for protection against severe COVID-19 in settings yet to offer boosters and suggests that individuals who received a ChAdOx1-S booster do not require re-vaccination ahead of others.

摘要

尽管已经有 ChAdOx1-S 加强型疫苗可用,但目前对于其实际效果知之甚少,尽管临床试验已经表明,ChAdOx1-S 加强型疫苗接种后可增强免疫力。在同一时期,英国有 43171 人接种了 ChAdOx1-S 加强型疫苗,而有 13038908 人接种了 BNT162b2 疫苗。ChAdOx1-S 加强型疫苗接种者更有可能是女性(调整后的优势比(OR)为 1.67(1.64-1.71)),处于临床风险组(调整后的 OR 为 1.58(1.54-1.63)),处于临床极度脆弱组(调整后的 OR 为 1.84(1.79-1.89))或严重免疫抑制(调整后的 OR 为 2.05(1.96-2.13))。在此,我们使用了一项测试阴性病例对照研究来估计 ChAdOx1-S 和 BNT162b2 加强型疫苗的有效性。针对 Omicron 变异株,ChAdOx1-S 和 BNT162b2 加强型疫苗对有症状疾病的保护作用峰值分别为 66.1%(16.6 至 86.3%)和 68.5%(65.7 至 71.2%),对老年人有效。针对住院治疗的保护作用峰值分别为 82.3%(64.2 至 91.3%)和 90.9%(88.7 至 92.7%)。对于 Delta,ChAdOx1-S 和 BNT162b2 加强型疫苗接种后,对住院治疗的有效性分别为 80.9%(15.6%至 95.7%)和 93.9%(92.8%至 94.9%)。本研究支持在尚未提供加强型疫苗的地区考虑接种 ChAdOx1-S 加强型疫苗以预防严重 COVID-19,并表明接种了 ChAdOx1-S 加强型疫苗的人不需要比其他人提前重新接种疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a642/9744823/5e06696bf869/41467_2022_35168_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a642/9744823/5e06696bf869/41467_2022_35168_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a642/9744823/5e06696bf869/41467_2022_35168_Fig1_HTML.jpg

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