PHH-1 V SARS-CoV-2 疫苗(Bimervax®)通过 HIPRA 诱导的变异特异性中和抗体水平

IF 4.5 3区 医学 Q2 IMMUNOLOGY
Anna England , Julia Sung , Meritxell Deulofeu , Laura Ferrer Soler , Bassam Hallis , Kelly Thomas , Sue Charlton
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引用次数: 0

摘要

由于自发的基因突变,特别是尖峰蛋白受体结合域(RBD)部分的突变,SARS-CoV-2 病毒变种继续以惊人的速度出现,这使得病毒更有可能逃脱免疫。迄今为止,通过全球初级和/或加强免疫活动获得的免疫力足以保护人口免受新出现的奥米克龙变种的感染。目前根据新变种更新疫苗抗原组成以增强免疫力的方法可能无法长期持续。如果变异产生的变种诱发的感染较轻,而现有疫苗(如 Bimervax®)仍有足够的保护作用,那么这种方法也可能是多余的,因为 Covid 正逐渐成为一种季节性疾病。通过测量接种 Bimervax® 的受试者血清中的中和抗体滴度,我们已经证明 Bimervax® 能够诱导对各种 SARS-CoV-2 变异株的免疫反应,包括诱导更严重感染的早期变异株和被发现产生较轻微感染的近期变异株。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Variant-specific neutralising antibodies levels induced by the PHH-1 V SARS-CoV-2 vaccine (Bimervax®) by HIPRA
SARS-CoV-2 virus variants continue to emerge at an alarming rate due to spontaneous genetic mutations, particularly in the spike protein receptor-binding domain (RBD) portion, which render the virus more likely to escape immunity. So far, the immunity obtained through global primary and/or booster immunisation campaigns has been sufficient to protect the population from new emerging variants of the Omicron lineage. The current approach to update vaccines' antigen composition to new variants to boost immunity may not be sustainable in the long term. It might also be potentially redundant if the mutations are giving rise to variants which induce milder infections and existing vaccines, such as Bimervax®, are still sufficiently protective, as Covid is slowly becoming a seasonal illness. Through measuring neutralising antibody titres in sera from subjects boosted with Bimervax®, we have demonstrated the ability of Bimervax® to induce immune responses against a variety of SARS-CoV-2 variants, ranging from earlier variants inducing more serious infections to more recent variants which have been found to produce milder infections.
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来源期刊
Vaccine
Vaccine 医学-免疫学
CiteScore
8.70
自引率
5.50%
发文量
992
审稿时长
131 days
期刊介绍: Vaccine is unique in publishing the highest quality science across all disciplines relevant to the field of vaccinology - all original article submissions across basic and clinical research, vaccine manufacturing, history, public policy, behavioral science and ethics, social sciences, safety, and many other related areas are welcomed. The submission categories as given in the Guide for Authors indicate where we receive the most papers. Papers outside these major areas are also welcome and authors are encouraged to contact us with specific questions.
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