Division of Epidemiology, School of Public Health, University of California, Berkeley, Berkeley, CA, 94720, USA.
Division of Infectious Diseases & Vaccinology, School of Public Health, University of California, Berkeley, Berkeley, CA, 94720, USA.
Nat Commun. 2023 Mar 14;14(1):1407. doi: 10.1038/s41467-023-37051-5.
Expansion of the SARS-CoV-2 BA.4 and BA.5 Omicron subvariants in populations with prevalent immunity from prior infection and vaccination, and associated burden of severe COVID-19, has raised concerns about epidemiologic characteristics of these lineages including their association with immune escape or severe clinical outcomes. Here we show that BA.4/BA.5 cases in a large US healthcare system had at least 55% (95% confidence interval: 43-69%) higher adjusted odds of prior documented infection than time-matched BA.2 cases, as well as 15% (9-21%) and 38% (27-49%) higher adjusted odds of having received 3 and ≥4 COVID-19 vaccine doses, respectively. However, after adjusting for differences in epidemiologic characteristics among cases with each lineage, BA.4/BA.5 infection was not associated with differential risk of emergency department presentation, hospital admission, or intensive care unit admission following an initial outpatient diagnosis. This finding held in sensitivity analyses correcting for potential exposure misclassification resulting from unascertained prior infections. Our results demonstrate that the reduced severity associated with prior (BA.1 and BA.2) Omicron lineages, relative to the Delta variant, has persisted with BA.4/BA.5, despite the association of BA.4/BA.5 with increased risk of breakthrough infection among previously vaccinated or infected individuals.
SARS-CoV-2 的 BA.4 和 BA.5 奥密克戎亚变种在先前感染和接种疫苗后具有普遍免疫力的人群中扩张,并且与严重 COVID-19 的负担相关,这引起了人们对这些谱系的流行病学特征的关注,包括它们与免疫逃逸或严重临床结果的关联。在这里,我们表明,在一个大型美国医疗保健系统中,BA.4/BA.5 病例与时间匹配的 BA.2 病例相比,先前有记录的感染的调整后优势比至少高 55%(95%置信区间:43-69%),分别有 15%(9-21%)和 38%(27-49%)更高的调整后优势比接受了 3 剂和≥4 剂 COVID-19 疫苗。然而,在调整了每种谱系病例之间的流行病学特征差异后,BA.4/BA.5 感染与急诊就诊、住院或初始门诊诊断后的重症监护病房入院的风险差异无关。在敏感性分析中,校正了由于先前未确定的感染而导致的潜在暴露错误分类的情况下,这一发现仍然成立。我们的研究结果表明,与 Delta 变体相比,先前(BA.1 和 BA.2)奥密克戎谱系的严重程度降低的情况在 BA.4/BA.5 中仍然存在,尽管 BA.4/BA.5 与先前接种过疫苗或感染过的个体的突破性感染风险增加有关。