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分析不同猴痘病毒抗原诱导的免疫血清的结合和真实病毒中和活性。

Analysis of binding and authentic virus-neutralizing activities of immune sera induced by various monkeypox virus antigens.

机构信息

Department of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Shenzhen Third People's Hospital and The Second Affiliated Hospital of Southern University of Science and Technology, Shenzhen, People's Republic of China.

BSL-3 Laboratory (Guangdong), Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical University, Guangzhou, People's Republic of China.

出版信息

Immunol Res. 2024 Oct;72(5):902-907. doi: 10.1007/s12026-024-09499-0. Epub 2024 Jun 3.

Abstract

Monkeypox cases continue to increase globally, and there is an urgent need to develop a highly effective vaccine against monkeypox. This study investigated the binding and authentic-virus neutralizing activities of sera from mice immunized with EEV (extracellularly enveloped viruses) antigens B6R and A35R, and IMV (intrinsic material viruses) antigens M1R, A29L, E8L, and H3L against monkeypox virus. The results showed that immunizations of A35R and E8L could only induce lower titers of binding antibodies, in contrast, immunization of M1R induced the highest titers of binding antibodies, while immunization of B6R, H3L, and A29L induced moderate titers of binding antibodies. For the live monkeypox virus neutralization assay, the results showed that immunization with two doses of EEV antigen B6R did not effectively induce humoral immune responses to neutralize monkeypox live virus, immunization with EEV-A35R only induced weak monkeypox-neutralizing antibodies. In contrast, the immunization of the four types of monkeypox virus IMV antigens can all induce neutralizing antibodies against authentic monkeypox virus, among them, A29L and H3L induced the highest neutralizing antibody titers. The results of this study provide important references for the selection of antigens in the development of the next generation of monkeypox vaccines.

摘要

猴痘病例在全球范围内继续增加,迫切需要开发一种针对猴痘的高效疫苗。本研究调查了用 EEV(细胞外包膜病毒)抗原 B6R 和 A35R 以及 IMV(内在材料病毒)抗原 M1R、A29L、E8L 和 H3L 免疫的小鼠血清对猴痘病毒的结合和真实病毒中和活性。结果表明,A35R 和 E8L 的免疫只能诱导较低滴度的结合抗体,相比之下,M1R 的免疫诱导了最高滴度的结合抗体,而 B6R、H3L 和 A29L 的免疫诱导了中等滴度的结合抗体。对于活猴痘病毒中和测定,结果表明,用两剂 EEV 抗原 B6R 免疫不能有效诱导中和活猴痘病毒的体液免疫反应,用 EEV-A35R 免疫仅诱导弱的猴痘中和抗体。相比之下,四种猴痘病毒 IMV 抗原的免疫都能诱导针对真实猴痘病毒的中和抗体,其中 A29L 和 H3L 诱导的中和抗体滴度最高。本研究结果为下一代猴痘疫苗开发中抗原的选择提供了重要参考。

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