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与SARS-CoV-2 BA.2.86/JN.1谱系相关的免疫逃逸和严重程度减弱

Immune escape and attenuated severity associated with the SARS-CoV-2 BA.2.86/JN.1 lineage.

作者信息

Lewnard Joseph A, Mahale Parag, Malden Debbie, Hong Vennis, Ackerson Bradley K, Lewin Bruno J, Link-Gelles Ruth, Feldstein Leora R, Lipsitch Marc, Tartof Sara Y

出版信息

medRxiv. 2024 Apr 19:2024.04.17.24305964. doi: 10.1101/2024.04.17.24305964.

Abstract

The SARS-CoV-2 BA.2.86 lineage, and its sublineage JN.1 in particular, achieved widespread transmission in the US during winter 2023-24. However, the increase in infections was not accompanied by increases in COVID-19 hospitalizations and mortality commensurate with prior waves. To understand shifts in COVID-19 epidemiology associated with JN.1 emergence, we compared characteristics and clinical outcomes of time-matched cases infected with BA.2.86- derived lineages (predominantly representing JN.1) versus co-circulating XBB-derived lineages in December, 2023 and January, 2024. Cases infected with BA.2.86-derived lineages received greater numbers of COVID-19 vaccine doses, including XBB.1.5-targeted and BA.4/BA.5-targeted boosters, in comparison to cases infected with XBB-derived lineages. Additionally, cases infected with BA.2.86-derived lineages experienced greater numbers of documented prior SARS-CoV-2 infections. These associations of BA.2.86-derived lineages with immune escape were confirmed when comparing cases diagnosed during periods when JN.1 was the predominant circulating lineage to cases diagnosed during November, 2023. Cases infected with BA.2.86-derived lineages, or during periods when JN.1 was the predominant circulating lineage, also experienced lower risk of progression to severe clinical outcomes requiring emergency department consultations or hospital admission. Sensitivity analyses suggested under-ascertainment of prior infections, even if differential between cases infected with BA.2.86-derived lineages and non-BA.2.86 lineages, could not explain this apparent attenuation of severity. Our findings implicate escape from immunity acquired from prior vaccination or infection in the emergence of the JN.1 lineage and suggest infections with this lineage are less likely to experience clinically-severe disease. Monitoring of immune escape and clinical severity in emerging SARS-CoV-2 variants remains a priority to inform responses.

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的BA.2.86谱系,尤其是其子谱系JN.1,在2023 - 2024年冬季在美国广泛传播。然而,感染人数的增加并未伴随着与之前几波疫情相当的新冠病毒住院率和死亡率的上升。为了解与JN.1出现相关的新冠病毒流行病学变化,我们比较了2023年12月和2024年1月感染BA.2.86衍生谱系(主要代表JN.1)与同时流行的XBB衍生谱系的时间匹配病例的特征和临床结局。与感染XBB衍生谱系的病例相比,感染BA.2.86衍生谱系的病例接种了更多剂新冠病毒疫苗,包括针对XBB.1.5和BA.4/BA.任5的加强针。此外,感染BA.2.86衍生谱系的病例既往有更多记录在案的SARS-CoV-2感染史。当比较JN.1为主要流行谱系期间诊断的病例与2023年11月诊断的病例时,BA.2.86衍生谱系与免疫逃逸的这些关联得到了证实。感染BA.2.86衍生谱系的病例,或在JN.1为主要流行谱系的时期,进展为需要急诊科会诊或住院治疗的严重临床结局的风险也较低。敏感性分析表明,即使BA.2.86衍生谱系感染病例与非BA.2.86谱系感染病例之间既往感染情况存在差异,既往感染的漏报也无法解释这种明显的严重程度减弱。我们的研究结果表明,JN.1谱系的出现与从既往疫苗接种或感染中获得的免疫力逃逸有关,并表明感染该谱系的病例发生临床严重疾病的可能性较小。监测新出现的SARS-CoV-2变体的免疫逃逸和临床严重程度仍然是为应对措施提供信息的优先事项。

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