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单细胞测序揭示恒河猴接种灭活肠道病毒 D68 疫苗的抗体反应

Single B cells reveal the antibody responses of rhesus macaques immunized with an inactivated enterovirus D68 vaccine.

机构信息

Institute of Medical Biology, Chinese Academy of Medical Sciences, Peking Union Medical College, Kunming, 650118, China.

Key Laboratory of Systemic Innovative Research on Virus Vaccine, Chinese Academy of Medical Sciences, Beijing, China.

出版信息

Arch Virol. 2020 Aug;165(8):1777-1789. doi: 10.1007/s00705-020-04676-6. Epub 2020 May 28.

Abstract

Enterovirus D68 (EV-D68) infection may cause severe respiratory system manifestations in pediatric populations. Because of the lack of an effective preventive vaccine or specific therapeutic drug for this infection, the development of EV-D68-specific vaccines and antibodies has become increasingly important. In this study, we prepared an experimental EV-D68 vaccine inactivated by formaldehyde and found that the serum of rhesus macaques immunized with the inactivated EV-D68 vaccine exhibited potent neutralizing activity against EV-D68 virus in vitro. Subsequently, the antibody-mediated immune response of B cells elicited by the inactivated vaccine was evaluated in a rhesus monkey model. The binding activity, in vitro neutralization activity, and sequence properties of 28 paired antibodies from the rhesus macaques' EV-D68-specific single memory B cells were analyzed, and the EV-D68 VP1-specific antibody group was found to be the main constituent in vivo. Intriguingly, we also found a synergistic effect among the E15, E18 and E20 monoclonal antibodies from the rhesus macaques. Furthermore, we demonstrated the protective efficacy of maternal antibodies in suckling C57BL/6 mice. This study provides valuable information for the future development of EV-D68 vaccines.

摘要

肠道病毒 D68(EV-D68)感染可能导致儿科人群出现严重的呼吸系统表现。由于缺乏针对这种感染的有效预防疫苗或特定治疗药物,因此开发 EV-D68 特异性疫苗和抗体变得越来越重要。在这项研究中,我们制备了一种甲醛灭活的实验性 EV-D68 疫苗,发现用灭活 EV-D68 疫苗免疫的恒河猴血清在体外对 EV-D68 病毒表现出强大的中和活性。随后,在恒河猴模型中评估了灭活疫苗引起的 B 细胞抗体介导的免疫反应。分析了 28 对来自恒河猴 EV-D68 特异性单记忆 B 细胞的配对抗体的结合活性、体外中和活性和序列特性,发现 EV-D68 VP1 特异性抗体组是体内的主要组成部分。有趣的是,我们还发现来自恒河猴的 E15、E18 和 E20 单克隆抗体之间存在协同作用。此外,我们证明了母源抗体在乳鼠 C57BL/6 中的保护效力。这项研究为 EV-D68 疫苗的未来发展提供了有价值的信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d483/8851307/04c8c4361682/705_2020_4676_Fig1_HTML.jpg

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