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本文引用的文献

1
Pre-Pandemic Cross-Reactive Immunity against SARS-CoV-2 among Central and West African Populations.大流行前中非人群对 SARS-CoV-2 的交叉反应性免疫。
Viruses. 2022 Oct 14;14(10):2259. doi: 10.3390/v14102259.
2
Effects of Antibody Responses to Pre-Existing Coronaviruses on Disease Severity and Complement Activation in COVID-19 Patients.针对既往冠状病毒的抗体反应对新冠患者疾病严重程度及补体激活的影响
Microorganisms. 2022 Jun 10;10(6):1191. doi: 10.3390/microorganisms10061191.
3
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
Lancet. 2022 Apr 16;399(10334):1513-1536. doi: 10.1016/S0140-6736(21)02796-3. Epub 2022 Mar 10.
4
Immune response to SARS-CoV-2 variants: A focus on severity, susceptibility, and preexisting immunity.针对 SARS-CoV-2 变异株的免疫反应:关注严重程度、易感性和预先存在的免疫。
J Infect Public Health. 2022 Feb;15(2):277-288. doi: 10.1016/j.jiph.2022.01.007. Epub 2022 Jan 13.
5
Cross-reactive memory T cells associate with protection against SARS-CoV-2 infection in COVID-19 contacts.交叉反应性记忆 T 细胞与 COVID-19 接触者对 SARS-CoV-2 感染的保护有关。
Nat Commun. 2022 Jan 10;13(1):80. doi: 10.1038/s41467-021-27674-x.
6
Pre-existing humoral immunity to human common cold coronaviruses negatively impacts the protective SARS-CoV-2 antibody response.既往针对人类普通感冒冠状病毒的体液免疫会对 SARS-CoV-2 抗体的保护性应答产生负面影响。
Cell Host Microbe. 2022 Jan 12;30(1):83-96.e4. doi: 10.1016/j.chom.2021.12.005. Epub 2021 Dec 7.
7
Pre-existing polymerase-specific T cells expand in abortive seronegative SARS-CoV-2.预先存在的聚合酶特异性 T 细胞在 SARS-CoV-2 无血清学阴性中扩增。
Nature. 2022 Jan;601(7891):110-117. doi: 10.1038/s41586-021-04186-8. Epub 2021 Nov 10.
8
Low-dose mRNA-1273 COVID-19 vaccine generates durable memory enhanced by cross-reactive T cells.低剂量 mRNA-1273 COVID-19 疫苗可产生由交叉反应性 T 细胞增强的持久记忆。
Science. 2021 Oct 22;374(6566):eabj9853. doi: 10.1126/science.abj9853.
9
High prevalence of pre-existing serological cross-reactivity against severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) in sub-Saharan Africa.撒哈拉以南非洲地区存在严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)血清学交叉反应的高流行率。
Int J Infect Dis. 2021 Jan;102:577-583. doi: 10.1016/j.ijid.2020.10.104. Epub 2020 Nov 8.
10
SARS-CoV-2-derived peptides define heterologous and COVID-19-induced T cell recognition.SARS-CoV-2 衍生肽定义了异源和 COVID-19 诱导的 T 细胞识别。
Nat Immunol. 2021 Jan;22(1):74-85. doi: 10.1038/s41590-020-00808-x. Epub 2020 Sep 30.

疫情前乌干达人中具有严重急性呼吸综合征冠状病毒2(SARS-CoV-2)交叉反应性CD4+和CD8+T细胞应答的比例较高。

High proportion of Ugandans with pre-pandemic SARS-CoV-2 cross-reactive CD4+ and CD8+ T-cell responses.

作者信息

Namuniina Annemarie, Muyanja Enoch S, Biribawa Victoria M, Okech Brenda A, Ssemaganda Aloysious, Price Matt A, Hills Nancy, Nanteza Ann, Bagaya Bernard Ssentalo, Weiskopf Daniela, Riou Catherine, Reynolds Steven J, Galwango Ronald M, Redd Andrew D

机构信息

UVRI-IAVI HIV Vaccine Program, Entebbe, Uganda.

Emory University, Department of Pathology and Laboratory Medicine.

出版信息

medRxiv. 2023 Jan 20:2023.01.16.23284626. doi: 10.1101/2023.01.16.23284626.

DOI:10.1101/2023.01.16.23284626
PMID:36711579
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9882430/
Abstract

The estimated mortality rate of the SARS-CoV-2 pandemic varied greatly around the world with multiple countries in East, Central, and West Africa having significantly lower rates of COVID-19 related fatalities than many resource-rich nations with significantly earlier wide-spread access to life-saving vaccines. One possible reason for this lower mortality could be the presence of pre-existing cross-reactive immunological responses in these areas of the world. To explore this hypothesis, stored peripheral blood mononuclear cells (PBMC) from Ugandans collected from 2015-2017 prior to the COVID-19 pandemic (n=29) and from hospitalized Ugandan COVID-19 patients (n=3) were examined using flow-cytometry for the presence of pre-existing SARS-CoV-2 cross-reactive CD4+ and CD8+ T-cell populations using four T-cell epitope mega pools. Of pre-pandemic participants, 89.7% (26/29) had either CD4+ or CD8+, or both, SARS-CoV-2 specific T-cell responses. Specifically, CD4+ T-cell reactivity (72.4%) and CD8+ T-cell reactivity (65.5%) were relatively similar, and 13 participants (44.8%) had both types of cross-reactive types of T-cells present. There were no significant differences in response by sex in the population. The rates of cross-reactive T-cell populations in these Ugandans is higher than previous estimates from resource-rich countries like the United States (20-50% reactivity). It is unclear what role, if any, this cross-reactivity played in decreasing COVID-19 related mortality in Uganda and other African countries, but does suggest that a better understanding of global pre-existing immunological cross-reactivity could be an informative data of epidemiological intelligence moving forward.

摘要

2019冠状病毒病大流行的估计死亡率在世界各地差异很大,东非、中非和西非的多个国家与许多资源丰富的国家相比,2019冠状病毒病相关死亡率显著较低,而这些资源丰富的国家更早广泛获得了救命疫苗。死亡率较低的一个可能原因是,世界这些地区存在预先存在的交叉反应性免疫反应。为了探究这一假设,利用流式细胞术,使用四个T细胞表位大池,检测了2015年至2017年在2019冠状病毒病大流行之前收集的乌干达人的储存外周血单核细胞(PBMC)(n = 29)和住院的乌干达2019冠状病毒病患者的外周血单核细胞(n = 3),以检测预先存在的2019冠状病毒病交叉反应性CD4+和CD8+ T细胞群体的存在。在大流行前的参与者中,89.7%(26/29)有CD4+或CD8+,或两者都有2019冠状病毒病特异性T细胞反应。具体而言,CD4+ T细胞反应性(72.4%)和CD8+ T细胞反应性(65.5%)相对相似,13名参与者(44.8%)同时存在两种交叉反应性T细胞类型。该人群中按性别划分的反应没有显著差异。这些乌干达人中交叉反应性T细胞群体的比例高于美国等资源丰富国家先前的估计(反应性为20 - 50%)。目前尚不清楚这种交叉反应性在降低乌干达和其他非洲国家2019冠状病毒病相关死亡率方面起到了什么作用(如果有的话),但这确实表明,更好地了解全球预先存在的免疫交叉反应性可能是未来流行病学情报的一个有益数据。