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美国大型医疗体系中,针对奥密克戎和德尔塔变异株,BNT162b2 疫苗对住院和急诊科就诊的持久性:一项病例对照研究。

Durability of BNT162b2 vaccine against hospital and emergency department admissions due to the omicron and delta variants in a large health system in the USA: a test-negative case-control study.

机构信息

Kaiser Permanente Southern California Department of Research & Evaluation, Pasadena, CA, USA; Department of Health Systems Science, Kaiser Permanente Bernard J. Tyson School of Medicine, Pasadena, CA USA.

Kaiser Permanente Southern California Department of Research & Evaluation, Pasadena, CA, USA.

出版信息

Lancet Respir Med. 2022 Jul;10(7):689-699. doi: 10.1016/S2213-2600(22)00101-1. Epub 2022 Apr 22.


DOI:10.1016/S2213-2600(22)00101-1
PMID:35468336
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9033225/
Abstract

BACKGROUND: The duration of protection against the omicron (B.1.1.529) variant for current COVID-19 vaccines is not well characterised. Vaccine-specific estimates are especially needed. We aimed to evaluate the effectiveness and durability of two and three doses of the BNT162b2 (Pfizer-BioNTech) mRNA vaccine against hospital and emergency department admissions due to the delta (B.1.617.2) and omicron variants. METHODS: In this case-control study with a test-negative design, we analysed electronic health records of members of Kaiser Permanente Southern California (KPSC), a large integrated health system in California, USA, from Dec 1, 2021, to Feb 6, 2022. Vaccine effectiveness was calculated in KPSC patients aged 18 years and older admitted to hospital or an emergency department (without a subsequent hospital admission) with a diagnosis of acute respiratory infection and tested for SARS-CoV-2 via PCR. Adjusted vaccine effectiveness was estimated with odds ratios from adjusted logistic regression models. This study is registered with ClinicalTrials.gov (NCT04848584). FINDINGS: Analyses were done for 11 123 hospital or emergency department admissions. In adjusted analyses, effectiveness of two doses of the BNT162b2 vaccine against the omicron variant was 41% (95% CI 21-55) against hospital admission and 31% (16-43) against emergency department admission at 9 months or longer after the second dose. After three doses, effectiveness of BNT162b2 against hospital admission due to the omicron variant was 85% (95% CI 80-89) at less than 3 months but fell to 55% (28-71) at 3 months or longer, although confidence intervals were wide for the latter estimate. Against emergency department admission, the effectiveness of three doses of BNT162b2 against the omicron variant was 77% (72-81) at less than 3 months but fell to 53% (36-66) at 3 months or longer. Trends in waning against SARS-CoV-2 outcomes due to the delta variant were generally similar, but with higher effectiveness estimates at each timepoint than those seen for the omicron variant. INTERPRETATION: Three doses of BNT162b2 conferred high protection against hospital and emergency department admission due to both the delta and omicron variants in the first 3 months after vaccination. However, 3 months after receipt of a third dose, waning was apparent against SARS-CoV-2 outcomes due to the omicron variant, including hospital admission. Additional doses of current, adapted, or novel COVD-19 vaccines might be needed to maintain high levels of protection against subsequent waves of SARS-CoV-2 caused by the omicron variant or future variants with similar escape potential. FUNDING: Pfizer.

摘要

背景:目前,针对新冠病毒 omicron(B.1.1.529)变异株的疫苗防护持续时间尚未得到很好的描述。特别是需要评估两剂和三剂 BNT162b2(辉瑞-生物科技)mRNA 疫苗对 delta(B.1.617.2)和 omicron 变异株导致的住院和急诊入院的有效性和持久性。

方法:本病例对照研究采用测试阴性设计,分析了美国加利福尼亚州 Kaiser Permanente Southern California(KPSC)的电子健康记录,该系统是一个大型综合性医疗系统。研究时间为 2021 年 12 月 1 日至 2022 年 2 月 6 日,研究对象为年龄在 18 岁及以上、因急性呼吸道感染住院或急诊就诊(无后续住院)且通过 PCR 检测 SARS-CoV-2 呈阳性的 KPSC 患者。使用调整后的逻辑回归模型计算的比值比来估计调整后的疫苗有效性。本研究在 ClinicalTrials.gov 注册(NCT04848584)。

结果:共分析了 11233 例住院或急诊就诊的患者。在调整分析中,两剂 BNT162b2 疫苗对 omicron 变异株的有效性为:第二剂后 9 个月或更长时间,预防住院的效力为 41%(95%CI 21-55),预防急诊就诊的效力为 31%(16-43)。接种三剂 BNT162b2 疫苗后,预防 omicron 变异株引起的住院的效力在接种后不到 3 个月时为 85%(95%CI 80-89),但在 3 个月或更长时间时下降至 55%(28-71),尽管后者的置信区间较宽。在预防急诊就诊方面,三剂 BNT162b2 对 omicron 变异株的有效性在接种后不到 3 个月时为 77%(72-81),但在 3 个月或更长时间时下降至 53%(36-66)。delta 变异株引起的 SARS-CoV-2 结果下降的趋势总体相似,但每个时间点的有效性估计值均高于 omicron 变异株。

结论:三剂 BNT162b2 疫苗在接种后 3 个月内对 delta 和 omicron 变异株引起的住院和急诊就诊均提供了高度保护。然而,在接种第三剂后 3 个月,预防 omicron 变异株引起的 SARS-CoV-2 结果的效力明显下降,包括住院治疗。可能需要接种当前、适应性或新型 COVID-19 疫苗的额外剂量,以维持对 omicron 变异株或未来具有类似逃逸潜力的变异株引起的 SARS-CoV-2 后续波的高保护水平。

资助:辉瑞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3c8/9033225/f7e8cb9b5849/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3c8/9033225/c0fc06e57441/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3c8/9033225/f7e8cb9b5849/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3c8/9033225/c0fc06e57441/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3c8/9033225/f7e8cb9b5849/gr2_lrg.jpg

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本文引用的文献

[1]
Estimated Effectiveness of COVID-19 Vaccines Against Omicron or Delta Symptomatic Infection and Severe Outcomes.

JAMA Netw Open. 2022-9-1

[2]
Protection by a Fourth Dose of BNT162b2 against Omicron in Israel.

N Engl J Med. 2022-5-5

[3]
Covid-19 Vaccine Effectiveness against the Omicron (B.1.1.529) Variant.

N Engl J Med. 2022-4-21

[4]
Effectiveness of mRNA-1273 against SARS-CoV-2 Omicron and Delta variants.

Nat Med. 2022-5

[5]
Waning 2-Dose and 3-Dose Effectiveness of mRNA Vaccines Against COVID-19-Associated Emergency Department and Urgent Care Encounters and Hospitalizations Among Adults During Periods of Delta and Omicron Variant Predominance - VISION Network, 10 States, August 2021-January 2022.

MMWR Morb Mortal Wkly Rep. 2022-2-18

[6]
SARS-CoV-2 vaccination induces immunological T cell memory able to cross-recognize variants from Alpha to Omicron.

Cell. 2022-3-3

[7]
SARS-CoV-2 Infection and Hospitalization Among Adults Aged ≥18 Years, by Vaccination Status, Before and During SARS-CoV-2 B.1.1.529 (Omicron) Variant Predominance - Los Angeles County, California, November 7, 2021-January 8, 2022.

MMWR Morb Mortal Wkly Rep. 2022-2-4

[8]
Divergent SARS-CoV-2 Omicron-reactive T and B cell responses in COVID-19 vaccine recipients.

Sci Immunol. 2022-3-25

[9]
Vaccines elicit highly conserved cellular immunity to SARS-CoV-2 Omicron.

Nature. 2022-3

[10]
T cell responses to SARS-CoV-2 spike cross-recognize Omicron.

Nature. 2022-3

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