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Durable antibody responses elicited by 1 dose of Ad26.COV2.S and substantial increase after boosting: 2 randomized clinical trials.1 剂 Ad26.COV2.S 诱导的持久抗体反应,并在加强后显著增加:2 项随机临床试验。
Vaccine. 2022 Jul 30;40(32):4403-4411. doi: 10.1016/j.vaccine.2022.05.047. Epub 2022 Jun 3.
2
Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Naturally Acquired Immunity versus Vaccine-induced Immunity, Reinfections versus Breakthrough Infections: A Retrospective Cohort Study.严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)自然获得性免疫与疫苗诱导免疫、再感染与突破感染:一项回顾性队列研究。
Clin Infect Dis. 2022 Aug 24;75(1):e545-e551. doi: 10.1093/cid/ciac262.
3
Long-term immunogenicity of BNT162b2 vaccination in older people and younger health-care workers.BNT162b2疫苗在老年人和年轻医护人员中的长期免疫原性。
Lancet Respir Med. 2021 Nov;9(11):e104-e105. doi: 10.1016/S2213-2600(21)00456-2. Epub 2021 Oct 20.
4
Effectiveness of mRNA BNT162b2 COVID-19 vaccine up to 6 months in a large integrated health system in the USA: a retrospective cohort study.辉瑞-BioNTech 信使核糖核酸 COVID-19 疫苗在美国大型综合卫生系统中的 6 个月有效性:一项回顾性队列研究。
Lancet. 2021 Oct 16;398(10309):1407-1416. doi: 10.1016/S0140-6736(21)02183-8. Epub 2021 Oct 4.
5
Booster shots for COVID-19-the debate continues.新冠病毒疫苗加强针——争论仍在继续。
Lancet Infect Dis. 2021 Oct;21(10):1359-1360. doi: 10.1016/S1473-3099(21)00574-0.
6
Efficacy of the mRNA-1273 SARS-CoV-2 Vaccine at Completion of Blinded Phase.mRNA-1273 新型冠状病毒疫苗在盲法阶段完成时的效力。
N Engl J Med. 2021 Nov 4;385(19):1774-1785. doi: 10.1056/NEJMoa2113017. Epub 2021 Sep 22.
7
The BNT162b2 vaccine effectiveness against new COVID-19 cases and complications of breakthrough cases: A nation-wide retrospective longitudinal multiple cohort analysis using individualised data.BNT162b2 疫苗对新的 COVID-19 病例和突破性病例并发症的有效性:使用个体数据进行的全国回顾性纵向多队列分析。
EBioMedicine. 2021 Oct;72:103574. doi: 10.1016/j.ebiom.2021.103574. Epub 2021 Sep 17.
8
Vaccination after prior COVID-19 infection: Implications for dose sparing and booster shots.既往感染过新冠病毒后的疫苗接种:对剂量节省和加强针的影响。
EBioMedicine. 2021 Oct;72:103586. doi: 10.1016/j.ebiom.2021.103586. Epub 2021 Sep 15.
9
Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine through 6 Months.辉瑞-BioNTech 信使核糖核酸新冠病毒疫苗 6 个月的安全性和有效性
N Engl J Med. 2021 Nov 4;385(19):1761-1773. doi: 10.1056/NEJMoa2110345. Epub 2021 Sep 15.
10
Protection of BNT162b2 Vaccine Booster against Covid-19 in Israel.辉瑞-BioNTech 疫苗加强针在以色列预防新冠病毒。
N Engl J Med. 2021 Oct 7;385(15):1393-1400. doi: 10.1056/NEJMoa2114255. Epub 2021 Sep 15.

针对已接种 COVID-19 疫苗的患者的加强针或额外疫苗接种剂量。

Booster or additional vaccination doses in patients vaccinated against COVID-19.

机构信息

Servicio de Microbiología Clínica y Enfermedades Infecciosas del Hospital General Universitario Gregorio Marañón, Universidad Complutense. CIBERES. Ciber de Enfermedades Respiratorias. Madrid, Spain.

出版信息

Rev Esp Quimioter. 2022 Apr;35(2):105-114. doi: 10.37201/req/149.2021. Epub 2021 Nov 15.

DOI:10.37201/req/149.2021
PMID:34775740
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8972704/
Abstract

Several health organizations, mainly in Western countries, have recently authorized the use of a booster dose of the COVID-19 vaccine for patients previously vaccinated with mRNA vaccines, with criteria that do not always coincide. The COVID Scientific Committee of the Illustrious College of Physicians of Madrid (ICOMEM) has received and asked several questions about this situation, to which the group has tried to give answers, after deliberation and consensus. The efficacy of the vaccines administered so far is beyond doubt and they have managed to reduce, fundamentally, the severe forms of the disease. The duration of this protection is not well known, is different in different individuals and for different variants of the virus and is not easily predictable with laboratory tests. Data on the real impact of a supplementary or "booster" dose in the scientific literature are scarce for the moment and its application in large populations such as those in the state of Israel may be associated with a decrease in the risk of new and severe episodes in the short observation period available. We also lack sufficient data on the safety and potential adverse effects of these supplementary doses and we do not know the ideal time to administer them in different situations. In this state of affairs, it seems prudent to administer supplemental doses to those exposed to a higher risk, such as immunocompromised individuals and the elderly. On the other hand, we consider that this is not the time to accelerate, on the spur of the moment, a massive administration of a third dose to other population groups that are less exposed and at lower risk, without waiting for adequate scientific information, which will undoubtedly arrive gradually. We do not believe that this position is incompatible with the practical and ethical warnings made by the World Health Organization in this respect.

摘要

一些卫生组织,主要在西方国家,最近授权对先前接种过 mRNA 疫苗的患者使用 COVID-19 疫苗加强针,其标准并不总是一致的。马德里杰出医师学院(ICOMEM)的 COVID 科学委员会收到并询问了有关这种情况的几个问题,经过审议和协商,该小组试图给出答案。迄今为止,已接种疫苗的功效是毋庸置疑的,它们基本上已经成功降低了疾病的严重程度。这种保护的持续时间尚不清楚,在不同个体和不同病毒变体之间是不同的,并且用实验室测试不易预测。目前,关于补充剂或“加强剂”剂量在科学文献中的实际影响的数据还很有限,其在以色列等国家的大量人群中的应用可能与在可获得的短期观察期内新的和严重发作风险降低有关。我们还缺乏关于这些补充剂量的安全性和潜在不良影响的足够数据,也不知道在不同情况下最佳的给药时间。在这种情况下,似乎明智的做法是对那些面临更高风险的人群(如免疫功能低下者和老年人)进行补充剂量的接种。另一方面,我们认为,现在还不是在没有足够科学信息的情况下,仓促地为其他暴露风险较低的人群加速接种第三剂疫苗的时候。我们不认为这种立场与世界卫生组织在这方面的实际和伦理警告不一致。