Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan; Program for Nurturing Global Leaders in Tropical and Emerging Communicable Diseases, Nagasaki University, Nagasaki, Japan; Department of Virology, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan; National Institute of Hygiene and Epidemiology, Hanoi, Vietnam.
Department of Virology, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Int J Infect Dis. 2024 Feb;139:109-117. doi: 10.1016/j.ijid.2023.11.008. Epub 2023 Nov 19.
SARS-CoV-2 transmission and epidemic potential is related to the population's immunity levels. As such, assessing different regions' preexisting immune responses to SARS-CoV-2 is important to understand the transmission potential of emerging SARS-CoV-2 variants.
In 975 serum samples from Vietnam (2014 to 2019), anti-SARS-CoV-2 Immunoglobulin G levels were determined by enzyme-linked immunosorbent assay. Plaque reduction neutralization test (PRNT) was performed using Wuhan strain and variants of concern (VOCs). Cross-reactivity was confirmed by analyzing B-cell receptor (BCR) repertoire sequences and identifying BCR repertoire sequences-derived T-cell epitopes.
Overall, 20.9% (n = 76/364) and 9.2% (n = 7) demonstrated SARS-CoV-2 neutralizing activity (PRNT) against the Wuhan and Alpha strain, respectively. Neutralizing activity against Beta, Gamma, and Delta strains was absent (PRNT<5) in all samples. Cross-reactive epitopes against SARS-CoV-2 and other coronavirus spike proteins were detected in the N-terminal domain, S2, and receptor-binding domain regions.
Following BCR and major histocompatibility complex analysis, T-cell receptor-recognized epitope motif (TREM) among pathogenic coronaviruses and coronaviruses spike proteins were the top TREM peptide, suggesting that pre-existing immunity against SARS-CoV-2 in Vietnam was due to exposure to common cold coronaviruses. With limited immunity against emerging VOCs, further monitoring, and control of the epidemic, along with COVID-19 vaccine programs against VOCs, are necessary.
SARS-CoV-2 的传播和流行潜力与人群的免疫水平有关。因此,评估不同地区人群对 SARS-CoV-2 的预先存在的免疫反应对于了解新兴 SARS-CoV-2 变异株的传播潜力非常重要。
在来自越南的 975 份血清样本(2014 年至 2019 年)中,通过酶联免疫吸附试验测定抗 SARS-CoV-2 免疫球蛋白 G 水平。使用武汉株和关注变异株(VOCs)进行噬斑减少中和试验(PRNT)。通过分析 B 细胞受体(BCR)库序列并鉴定 BCR 库序列衍生的 T 细胞表位来确认交叉反应性。
总体而言,有 20.9%(n=76/364)和 9.2%(n=7)的血清样本对武汉株和 Alpha 株具有 SARS-CoV-2 中和活性(PRNT)。所有样本对 Beta、Gamma 和 Delta 株的中和活性均为阴性(PRNT<5)。在 N 端结构域、S2 和受体结合结构域中检测到针对 SARS-CoV-2 和其他冠状病毒刺突蛋白的交叉反应性表位。
在 BCR 和主要组织相容性复合体分析之后,致病性冠状病毒和冠状病毒刺突蛋白之间的 T 细胞受体识别表位基序(TREM)是顶级 TREM 肽,表明越南人群对 SARS-CoV-2 的预先存在的免疫是由于暴露于普通感冒冠状病毒。由于对新兴 VOCs 的免疫力有限,因此需要进一步监测和控制疫情,并开展针对 VOCs 的 COVID-19 疫苗接种计划。