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HIV 感染者的 COVID-19 疫苗免疫原性。

COVID-19 vaccine immunogenicity in people with HIV.

机构信息

Division of Infectious Diseases/Chronic Viral Illness Service, McGill University Health Centre, Royal Victoria Hospital.

Infectious Diseases and Immunity in Global Health Research Institute of the McGill University Health Centre.

出版信息

AIDS. 2023 Jan 1;37(1):F1-F10. doi: 10.1097/QAD.0000000000003429. Epub 2022 Nov 18.

Abstract

OBJECTIVES

Many vaccines require higher/additional doses or adjuvants to provide adequate protection for people with HIV (PWH). Our objective was to compare COVID-19 vaccine immunogenicity in PWH to HIV-negative individuals.

DESIGN

In a Canadian multi-center prospective, observational cohort of PWH receiving at least two COVID-19 vaccinations, we measured vaccine-induced immunity at 3 and 6 months post 2nd and 1-month post 3rd doses.

METHODS

The primary outcome was the percentage of PWH mounting vaccine-induced immunity [co-positivity for anti-IgG against SARS-CoV2 Spike(S) and receptor-binding domain proteins] 6 months post 2nd dose. Univariable and multivariable logistic regressions were used to compare COVID-19-specific immune responses between groups and within subgroups.

RESULTS

Data from 294 PWH and 267 controls were analyzed. Immunogenicity was achieved in over 90% at each time point in both groups. The proportions of participants achieving comparable anti-receptor-binding domain levels were similar between the group at each time point. Anti-S IgG levels were similar by group at month 3 post 2nd dose and 1-month post 3rd dose. A lower proportion of PWH vs. controls maintained vaccine-induced anti-S IgG immunity 6 months post 2nd dose [92% vs. 99%; odds ratio: 0.14 (95% confidence interval: 0.03, 0.80; P = 0.027)]. In multivariable analyses, neither age, immune non-response, multimorbidity, sex, vaccine type, or timing between doses were associated with reduced IgG response.

CONCLUSION

Vaccine-induced IgG was elicited in the vast majority of PWH and was overall similar between groups. A slightly lower proportion of PWH vs. controls maintained vaccine-induced anti-S IgG immunity 6 months post 2nd dose demonstrating the importance of timely boosting in this population.

摘要

目的

许多疫苗需要更高/额外剂量或佐剂,以为艾滋病毒感染者(PLHIV)提供足够的保护。我们的目的是比较 PLHIV 与 HIV 阴性个体对 COVID-19 疫苗的免疫原性。

设计

在加拿大多中心前瞻性观察性 PLHIV 队列中,我们至少接受了两剂 COVID-19 疫苗,在第 2 剂后 3 个月和第 3 剂后 1 个月测量疫苗诱导的免疫。

方法

主要结局是第 2 剂后 6 个月时,PLHIV 产生疫苗诱导免疫的百分比[针对 SARS-CoV2 刺突(S)和受体结合域蛋白的抗 IgG 共阳性]。使用单变量和多变量逻辑回归比较两组之间和亚组内的 COVID-19 特异性免疫反应。

结果

共分析了 294 名 PLHIV 和 267 名对照者的数据。两组在每个时间点的免疫原性均超过 90%。两组在每个时间点达到可比抗受体结合域水平的参与者比例相似。第 2 剂后 3 个月和第 3 剂后 1 个月,抗-S IgG 水平在组间相似。与对照组相比,PLHIV 维持第 2 剂后 6 个月疫苗诱导的抗-S IgG 免疫的比例较低[92%比 99%;比值比:0.14(95%置信区间:0.03,0.80;P=0.027)]。多变量分析显示,年龄、免疫无反应、多种合并症、性别、疫苗类型或剂量间隔均与 IgG 反应降低无关。

结论

疫苗诱导的 IgG 在绝大多数 PLHIV 中被激发,总体上两组之间相似。与对照组相比,PLHIV 维持第 2 剂后 6 个月疫苗诱导的抗-S IgG 免疫的比例略低,这表明在该人群中及时加强免疫的重要性。

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