BACKGROUND: The Omicron variant has challenged the control of the COVID-19 pandemic due to its immuno-evasive properties. The administration of a booster dose of a SARS-CoV-2 vaccine showed positive effects in the immunogenicity against SARS-CoV-2, effect that is even enhanced after the administration of a second booster. METHODS: During a phase-3 clinical trial, we evaluated the effect of a second booster of CoronaVac®, an inactivated vaccine administered 6 months after the first booster, in the neutralization of SARS-CoV-2 (n = 87). In parallel, cellular immunity (n = 45) was analyzed in stimulated peripheral mononuclear cells by flow cytometry and ELISPOT. FINDINGS: Although a 2.5-fold increase in neutralization of the ancestral SARS-CoV-2 was observed after the second booster when compared with prior its administration (Geometric mean units p < 0.0001; Geometric mean titer p = 0.0002), a poor neutralization against the Omicron variant was detected. Additionally, the activation of specific CD4(+) T lymphocytes remained stable after the second booster and, importantly, equivalent activation of CD4(+) T lymphocytes against the Omicron variant and the ancestral SARS-CoV-2 were found. INTERPRETATION: Although the neutralizing response against the Omicron variant after the second booster of CoronaVac® was slightly increased, these levels are far from those observed against the ancestral SARS-CoV-2 and could most likely fail to neutralize the virus. In contrast, a robust CD4(+)T cell response may confer protection against the Omicron variant. FUNDING: The Ministry of Health, Government of Chile, the Confederation of Production and Commerce, Chile and SINOVAC Biotech.NIHNIAID. The Millennium Institute on Immunology and Immunotherapy.
Humoral and cellular response induced by a second booster of an inactivated SARS-CoV-2 vaccine in adults.
成人接种第二剂灭活SARS-CoV-2疫苗加强针后引起的体液和细胞反应
阅读:4
作者:Méndez Constanza, Peñaloza Hernán F, Schultz Bárbara M, Piña-Iturbe Alejandro, RÃos Mariana, Moreno-Tapia Daniela, Pereira-Sánchez Patricia, Leighton Diane, Orellana Claudia, Covarrubias Consuelo, Gálvez Nicolás M S, Soto Jorge A, Duarte Luisa F, Rivera-Pérez Daniela, Vázquez Yaneisi, Cabrera Alex, Bustos Sergio, Iturriaga Carolina, Urzua Marcela, Navarrete MarÃa S, Rojas Ãlvaro, Fasce Rodrigo A, Fernández Jorge, Mora Judith, RamÃrez Eugenio, Gaete-Argel Aracelly, Acevedo Mónica, Valiente-EcheverrÃa Fernando, Soto-Rifo Ricardo, Weiskopf Daniela, Grifoni Alba, Sette Alessandro, Zeng Gang, Meng Weining, González-Aramundiz José V, González Pablo A, Abarca Katia, Melo-González Felipe, Bueno Susan M, Kalergis Alexis M
| 期刊: | EBioMedicine | 影响因子: | 10.800 |
| 时间: | 2023 | 起止号: | 2023 May;91:104563 |
| doi: | 10.1016/j.ebiom.2023.104563 | 研究方向: | 细胞生物学 |
| 疾病类型: | 新冠 | ||
特别声明
1、本文转载旨在传播信息,不代表本网站观点,亦不对其内容的真实性承担责任。
2、其他媒体、网站或个人若从本网站转载使用,必须保留本网站注明的“来源”,并自行承担包括版权在内的相关法律责任。
3、如作者不希望本文被转载,或需洽谈转载稿费等事宜,请及时与本网站联系。
4、此外,如需投稿,也可通过邮箱info@biocloudy.com与我们取得联系。
