Yang Xueying, Zhang Jiajia, Liu Ziang, Chen Shujie, Weissman Sharon, Poland Gregory A, Phaswana-Mafuya Refilwe Nancy, Olatosi Bankole, Li Xiaoming
Department of Health Promotion, Education and Behavior, Arnold School of Public Health, University of South Carolina, Columbia, USA; South Carolina SmartState Center for Healthcare Quality, University of South Carolina, Columbia, USA.
South Carolina SmartState Center for Healthcare Quality, University of South Carolina, Columbia, USA; Department of Epidemiology and Biostatistics, Arnold School of Public Health, University of South Carolina, Columbia, USA.
Int J Infect Dis. 2025 Jan;150:107310. doi: 10.1016/j.ijid.2024.107310. Epub 2024 Nov 23.
We estimated vaccine effectiveness (VE) against SARS-CoV-2 infection among a statewide cohort of people with HIV (PWH) and compared the estimates with a matched cohort of people without HIV (PWoH) in South Carolina (SC), USA.
A population-based cohort was retrieved from statewide electronic health records between January 2, 2021, and April 14, 2022, during which several variants were circulating in SC (i.e., Alpha, Delta, Omicron). We compared the odds of vaccination between test-positive cases and test-negative controls using logistic regression models for both SARS-CoV-2 infection and severe COVID-19 outcomes. The VE was derived as (1 - adjusted odds ratio) × 100%.
A total of 7279 test episodes in PWH and 72,790 matched test episodes in PWoH were included for analysis, representing 6561 unique PWH and 67,521 unique PWoH. The peak level of VE against SARS-CoV-2 infection occurred 7-59 days after receipt of the second dose of vaccine (PWH: 61.20%; PWoH: 67.09%), followed by a waning protective effect 90-119 days after the second dose in both PWH (35.80%) and PWoH (47.57%), where PWH had a proportionally lower and declined faster VE. Regarding the VE against severe outcomes of SARS-CoV-2 infection, a relatively higher level of protection was maintained in both populations (complete primary series: PWH: 69.06%; PWoH: 60.63%).
A complete primary series of COVID-19 vaccines offered significant protection against SARS-CoV-2 infection and severe outcomes in both PWH and PWoH populations, although this wanes with time. However, the estimate of VE against SARS-CoV-2 infection appeared lower in PWH than in PWoH and the degree of waning over time was relatively quicker in PWH.
我们估计了美国南卡罗来纳州(SC)全州范围内感染人类免疫缺陷病毒(HIV)的人群(PWH)中针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染的疫苗效力(VE),并将这些估计值与匹配的未感染HIV的人群(PWoH)队列进行比较。
从2021年1月2日至2022年4月14日的全州电子健康记录中检索了一个基于人群的队列,在此期间几种变体在SC传播(即阿尔法、德尔塔、奥密克戎)。我们使用逻辑回归模型比较了SARS-CoV-2感染和严重冠状病毒病(COVID-19)结局的检测呈阳性病例和检测呈阴性对照之间的疫苗接种几率。VE的计算方法为(1 - 调整后的优势比)×100%。
共纳入了PWH中的7279次检测事件和PWoH中的72790次匹配检测事件进行分析,分别代表6561名独特的PWH和67521名独特的PWoH。针对SARS-CoV-2感染的VE峰值出现在接种第二剂疫苗后的7 - 59天(PWH:61.20%;PWoH:67.09%),随后在第二剂疫苗接种后的90 - 119天保护作用减弱(PWH为35.80%,PWoH为47.57%),其中PWH的VE比例较低且下降更快。关于针对SARS-CoV-2感染严重结局的VE,两个群体均维持了相对较高的保护水平(完成初级系列接种:PWH:69.06%;PWoH:60.63%)。
完整的初级系列新型冠状病毒肺炎(COVID-19)疫苗在PWH和PWoH人群中均提供了针对SARS-CoV-2感染和严重结局的显著保护,尽管这种保护会随时间减弱。然而,PWH中针对SARS-CoV-2感染的VE估计值似乎低于PWoH,且随着时间推移减弱的程度在PWH中相对更快。