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Vaccines (Basel). 2022 Sep 3;10(9):1458. doi: 10.3390/vaccines10091458.
2
The COVID-19 Pandemic in a Hispanic Population: A Primary Care Perspective.《西班牙裔人群中的 COVID-19 大流行:初级保健视角》。
J Am Board Fam Med. 2022 Jul-Aug;35(4):686-694. doi: 10.3122/jabfm.2022.04.210163.
3
Neutralization Escape by SARS-CoV-2 Omicron Subvariants BA.2.12.1, BA.4, and BA.5.严重急性呼吸综合征冠状病毒2型奥密克戎亚变体BA.2.12.1、BA.4和BA.5的中和逃逸
N Engl J Med. 2022 Jul 7;387(1):86-88. doi: 10.1056/NEJMc2206576. Epub 2022 Jun 22.
4
BA.2.12.1, BA.4 and BA.5 escape antibodies elicited by Omicron infection.BA.2.12.1、BA.4 和 BA.5 逃避奥密克戎感染诱导的抗体。
Nature. 2022 Aug;608(7923):593-602. doi: 10.1038/s41586-022-04980-y. Epub 2022 Jun 17.
5
Durability of the Single-Dose Ad26.COV2.S Vaccine in the Prevention of COVID-19 Infections and Hospitalizations in the US Before and During the Delta Variant Surge.单剂量Ad26.COV2.S疫苗在美国德尔塔变种激增之前及期间预防新冠病毒感染和住院的持久性
JAMA Netw Open. 2022 Mar 1;5(3):e222959. doi: 10.1001/jamanetworkopen.2022.2959.
6
Estimating excess mortality due to the COVID-19 pandemic: a systematic analysis of COVID-19-related mortality, 2020-21.估算2019冠状病毒病大流行造成的超额死亡率:2020 - 2021年与2019冠状病毒病相关死亡率的系统分析
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COVID restrictions are lifting - what scientists think.新冠疫情限制措施正在解除——科学家们的看法。
Nature. 2022 Mar;603(7902):563. doi: 10.1038/d41586-022-00620-7.
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A Perspective on the Roles of Adjuvants in Developing Highly Potent COVID-19 Vaccines.关于佐剂在开发高效 COVID-19 疫苗中的作用的观点。
Viruses. 2022 Feb 14;14(2):387. doi: 10.3390/v14020387.
9
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.mRNA 疫苗对 COVID-19 相关急诊科和紧急护理就诊以及成人住院的 2 剂和 3 剂效力下降在德尔塔和奥密克戎变异主导期间 - VISION 网络,10 个州,2021 年 8 月至 2022 年 1 月。
MMWR Morb Mortal Wkly Rep. 2022 Feb 18;71(7):255-263. doi: 10.15585/mmwr.mm7107e2.
10
Performance Evaluation of Lateral Flow Assays for Coronavirus Disease-19 Serology.用于新型冠状病毒病血清学的侧向流动分析的性能评估。
Clin Lab Med. 2022 Mar;42(1):31-56. doi: 10.1016/j.cll.2021.10.005. Epub 2021 Nov 3.

评估强生公司新冠疫苗在低收入西班牙裔人群中的接种效果。

Evaluating Johnson and Johnson COVID-19 Vaccination Outcomes in a Low-Income Hispanic Population.

作者信息

Lamb Christopher, Owens Christopher, Gamboa Wendy, Lopez-Yunez Alfredo

机构信息

Weatherhead School of Management, Case Western Reserve University, Cleveland, OH 44106, USA.

Alivio Medical Center, Indianapolis, IN 46219, USA.

出版信息

Vaccines (Basel). 2023 Jan 10;11(1):148. doi: 10.3390/vaccines11010148.

DOI:10.3390/vaccines11010148
PMID:36679993
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9865710/
Abstract

BACKGROUND

A pilot study was performed at a low-income emergency care clinic to assess the humoral immune response to the Johnson & Johnson (J&J) COVID-19 vaccine (Ad26.COV2.S) to better understand how to evaluate the COVID-19 health status of its Hispanic patient population following vaccination.

METHODS

This study used the Clungene SARS-CoV-2 IgG/IgM Rapid Test Cassette to determine the presence of binding antibodies resulting from the J&J COVID-19 vaccine. The Clungene test principle is based on the receptor-binding domain (RBD) of the spike protein. Antibodies targeting the spike protein are considered an appropriate measure of humoral response from spike-based vaccines.

RESULTS

The study confirmed previous research that antibodies wane over time, and results are consistent with reported vaccine efficacy. There was a statistically significant relationship between the humoral immune response and demographic and health status variables.

CONCLUSIONS

COVID-19 negative patients can be easily and efficiently monitored to determine the success and durability of COVID-19 vaccines in low-income minority populations. The use of simple low-cost spike targeted COVID-19 antibody lateral flow devices may serve as a useful adjunct to assist community-based physicians on the COVID-19 health status of its patients. Further research is needed to confirm the utility of this approach.

摘要

背景

在一家低收入急诊诊所进行了一项试点研究,以评估对强生公司(J&J)新冠疫苗(Ad26.COV2.S)的体液免疫反应,以便更好地了解如何评估其西班牙裔患者群体接种疫苗后的新冠健康状况。

方法

本研究使用Clungene SARS-CoV-2 IgG/IgM快速检测试剂盒来确定强生新冠疫苗产生的结合抗体的存在情况。Clungene检测原理基于刺突蛋白的受体结合域(RBD)。针对刺突蛋白的抗体被认为是基于刺突蛋白的疫苗体液反应的合适指标。

结果

该研究证实了先前的研究结果,即抗体随时间减弱,且结果与报道的疫苗效力一致。体液免疫反应与人口统计学和健康状况变量之间存在统计学上的显著关系。

结论

对于新冠病毒检测呈阴性的患者,可以轻松且高效地进行监测,以确定新冠疫苗在低收入少数族裔人群中的效果和持久性。使用简单、低成本的针对刺突蛋白的新冠抗体侧向流动检测设备,可能有助于社区医生了解其患者的新冠健康状况。需要进一步研究来证实这种方法的实用性。