Shandong Provincial Key Laboratory of Infectious Disease Control and Prevention, Shandong Provincial Center for Disease Control and Prevention, Jinan 250014, China.
State Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing 100071, China; Department of Laboratory Medicine, Handan Central Hospital, Hebei Medical University, Handan 056001, China; Hebei Key Laboratory of Immune Mechanism of Major Infectious Diseases and New Technology of Diagnosis and Treatment, The Fifth Hospital of Shijiazhuang, Shijiazhuang 050021, China.
Cell Rep. 2024 Jul 23;43(7):114387. doi: 10.1016/j.celrep.2024.114387. Epub 2024 Jun 18.
The ongoing emergence of SARS-CoV-2 variants poses challenges to the immunity induced by infections and vaccination. We conduct a 6-month longitudinal evaluation of antibody binding and neutralization of sera from individuals with six different combinations of vaccination and infection against BA.5, XBB.1.5, EG.5.1, and BA.2.86. We find that most individuals produce spike-binding IgG or neutralizing antibodies against BA.5, XBB.1.5, EG.5.1, and BA.2.86 2 months after infection or vaccination. However, compared to ancestral strain and BA.5 variant, XBB.1.5, EG.5.1, and BA.2.86 exhibit comparable but significant immune evasion. The spike-binding IgG and neutralizing antibody titers decrease in individuals without additional antigen exposure, and <50% of individuals neutralize XBB.1.5, EG.5.1, and BA.2.86 during the 6-month follow-up. Approximately 57% of the 107 followed up individuals experienced an additional infection, leading to improved binding IgG and neutralizing antibody levels against these variants. These findings provide insights into the impact of SARS-CoV-2 variants on immunity following repeated exposure.
持续出现的 SARS-CoV-2 变体对感染和疫苗接种所诱导的免疫带来了挑战。我们对来自不同感染和接种组合个体的血清进行了 6 个月的纵向评估,这些个体针对 BA.5、XBB.1.5、EG.5.1 和 BA.2.86 进行了感染和接种。我们发现,大多数个体在感染或接种后 2 个月内会产生针对 BA.5、XBB.1.5、EG.5.1 和 BA.2.86 的刺突结合 IgG 或中和抗体。然而,与原始株和 BA.5 变体相比,XBB.1.5、EG.5.1 和 BA.2.86 表现出可比较但显著的免疫逃避。在没有额外抗原暴露的个体中,刺突结合 IgG 和中和抗体滴度下降,并且在 6 个月的随访中,只有不到 50%的个体能够中和 XBB.1.5、EG.5.1 和 BA.2.86。约 57%的 107 名随访个体经历了额外的感染,这导致针对这些变体的结合 IgG 和中和抗体水平得到了改善。这些发现提供了对 SARS-CoV-2 变体在反复暴露后对免疫影响的深入了解。