血清学多重免疫测定 (MIA) 可检测利比里亚 SARS-CoV-2 和其他病毒病原体的抗体反应性,并可配置为多重抑制试验 (MINT)

Immuno Pub Date : 2024-03-03 DOI:10.3390/immuno4010007
Brien K. Haun, Albert To, Caitlin A. Williams, Aquena H. Ball, Karalyn Fong, Teri Ann S. Wong, Bode Shobayo, Julius Teahton, Lauren L. Ching, Varney Kamara, Davidetta M. Tekah, Peter Humphrey, John Berestecky, Vivek R. Nerurkar, A. Lehrer
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引用次数: 0

摘要

SARS-CoV-2 大流行激发了全球迅速开发检测、治疗和疫苗的努力。然而,这些努力的成果迟迟未能惠及非洲大陆和全球许多中低收入国家(LMIC)。因此,我们开发了两种基于微珠的多重血清学检测方法,以确定利比里亚四个县的 SARS-CoV-2 暴露情况。这项研究于 2021 年夏季在大巴萨州、邦州、马吉比州和蒙特塞拉多州收集的 189 份样本中进行。我们的多重免疫测定(MIA)检测到 SARS-CoV-2 和多种变异抗原的暴露量升高。此外,我们还检测到暴露于登革热病毒血清型 2、基孔肯雅病毒和季节性冠状病毒 NL63 的证据。我们的多重抑制试验(MINT)是在 MIA 的基础上开发的,用于观察抗体介导的 SARS-CoV-2 尖峰蛋白与其同源细胞受体 ACE-2 结合的抑制作用。我们在接受测试的利比里亚样本中检测到了抑制性抗体,这些抗体总体上与恢复期血清学特征一致。这些互补性检测方法有助于补充现有的血清学检测需求,并可提高全球科学代表性不足地区的技术能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Serological Multiplexed Immunoassay (MIA) Detects Antibody Reactivity to SARS-CoV-2 and Other Viral Pathogens in Liberia and Is Configurable as a Multiplexed Inhibition Test (MINT)
The SARS-CoV-2 pandemic ignited global efforts to rapidly develop testing, therapeutics, and vaccines. However, the rewards of these efforts were slow to reach many low- to middle-income countries (LMIC) across the African continent and globally. Therefore, two bead-based multiplexed serological assays were developed to determine SARS-CoV-2 exposure across four counties in Liberia. This study was conducted during the summer of 2021 on 189 samples collected throughout Grand Bassa, Bong, Margibi, and Montserrado counties. Our multiplexed immunoassay (MIA) detected elevated exposure to SARS-CoV-2 and multiple variant antigens. Additionally, we detected evidence of exposure to Dengue virus serotype 2, Chikungunya virus, and the seasonal coronavirus NL63. Our multiplexed inhibition test (MINT) was developed from the MIA to observe antibody-mediated inhibition of SARS-CoV-2 spike protein binding to its cognate cellular receptor ACE-2. We detected inhibitory antibodies in the tested Liberian samples, which were collectively consistent with a convalescent serological profile. These complementary assays serve to supplement existing serological testing needs and may enhance the technical capacity of scientifically underrepresented regions globally.
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