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Initial SARS-CoV-2 vaccination response can predict booster response for BNT162b2 but not for AZD1222.初次接种 SARS-CoV-2 疫苗的反应可以预测 BNT162b2 的加强针反应,但不能预测 AZD1222 的加强针反应。
Int J Infect Dis. 2021 Sep;110:309-313. doi: 10.1016/j.ijid.2021.07.063. Epub 2021 Jul 28.

本文引用的文献

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FDA-authorized mRNA COVID-19 vaccines are effective per real-world evidence synthesized across a multi-state health system.FDA 授权的 mRNA COVID-19 疫苗根据多州医疗系统综合的真实世界证据有效。
Med. 2021 Aug 13;2(8):979-992.e8. doi: 10.1016/j.medj.2021.06.007. Epub 2021 Jun 29.
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Longitudinal analysis of humoral immunity against SARS-CoV-2 Spike in convalescent individuals up to 8 months post-symptom onset.症状出现后长达8个月的康复个体中针对SARS-CoV-2刺突蛋白体液免疫的纵向分析。
Cell Rep Med. 2021 Jun 15;2(6):100290. doi: 10.1016/j.xcrm.2021.100290. Epub 2021 May 5.
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COVID-19 dynamics after a national immunization program in Israel.以色列全国免疫计划后 COVID-19 动态。
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Nat Med. 2021 May;27(5):917-924. doi: 10.1038/s41591-021-01318-5. Epub 2021 Mar 26.
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Early rate reductions of SARS-CoV-2 infection and COVID-19 in BNT162b2 vaccine recipients.BNT162b2疫苗接种者中SARS-CoV-2感染和新冠肺炎的早期感染率降低情况。
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Early induction of functional SARS-CoV-2-specific T cells associates with rapid viral clearance and mild disease in COVID-19 patients.在 COVID-19 患者中,功能性 SARS-CoV-2 特异性 T 细胞的早期诱导与快速病毒清除和轻症疾病相关。
Cell Rep. 2021 Feb 9;34(6):108728. doi: 10.1016/j.celrep.2021.108728. Epub 2021 Jan 21.
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B cell memory: understanding COVID-19.B 细胞记忆:了解 COVID-19。
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Adaptive immunity to SARS-CoV-2 and COVID-19.对 SARS-CoV-2 和 COVID-19 的适应性免疫。
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Interim Results of a Phase 1-2a Trial of Ad26.COV2.S Covid-19 Vaccine.Ad26.COV2.S 新冠疫苗 1/2a 期临床试验的中期结果。
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当前抗SARS-CoV-2疫苗的难题。

The conundrum of current anti-SARS-CoV-2 vaccines.

作者信息

Federico Maurizio

机构信息

National Center for Global Health, Istituto Superiore di Sanità, Viale Regina Elena, 299, 00161, Rome, Italy.

出版信息

Cytokine Growth Factor Rev. 2021 Aug;60:46-51. doi: 10.1016/j.cytogfr.2021.03.001. Epub 2021 Mar 6.

DOI:10.1016/j.cytogfr.2021.03.001
PMID:33714693
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7936752/
Abstract

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has given rise to the urgent need for vaccines and therapeutic interventions to address the spread of the SARS-CoV-2 virus. SARS-CoV-2 vaccines in development, and those being distributed currently, have been designed to induce neutralizing antibodies using the spike protein of the virus as an immunogen. However, the immunological correlates of protection against the virus remain unknown. This raises questions about the efficacy of current vaccination strategies. In addition, safety profiles of several vaccines seem inadequate or have not yet been evaluated under controlled experimentation. Here, evidence from the literature regarding the efforts already made to identify the immunological correlates of protection against SARS-CoV-2 infection are summarized. Furthermore, key biological features of most of the advanced vaccines and considerations regarding their safety and expected efficacy are highlighted.

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)大流行引发了对疫苗和治疗性干预措施的迫切需求,以应对SARS-CoV-2病毒的传播。正在研发以及目前正在分发的SARS-CoV-2疫苗,设计为使用病毒的刺突蛋白作为免疫原诱导中和抗体。然而,针对该病毒的保护性免疫相关因素仍不清楚。这引发了关于当前疫苗接种策略有效性的问题。此外,几种疫苗的安全性似乎不足,或者尚未在对照实验中进行评估。在此,总结了文献中关于已为确定针对SARS-CoV-2感染的保护性免疫相关因素所做努力的证据。此外,还强调了大多数先进疫苗的关键生物学特性以及有关其安全性和预期疗效的考量。