Pardo Isabele, Maezato Aline Miho, Callado Gustavo Yano, Gutfreund Maria Celidonio, Hsieh Mariana Kim, Lin Vivian, Kobayashi Takaaki, Salinas Jorge L, Subramanian Aruna, Edmond Michael B, Diekema Daniel J, Rizzo Luiz Vicente, Marra Alexandre R
Faculdade Israelita de Ciências da Saúde Albert Einstein, Hospital Israelita Albert Einstein, São Paulo, SP, Brazil.
Department of Internal Medicine, University of Iowa Carver College of Medicine, Iowa City, IA, USA.
Antimicrob Steward Healthc Epidemiol. 2024 Sep 26;4(1):e152. doi: 10.1017/ash.2024.369. eCollection 2024.
We assessed the effectiveness of heterologous vaccination strategy in immunocompromised individuals regarding COVID-19 outcomes, comparing it to homologous approaches.
Systematic literature review/meta-analysis.
We searched PubMed, CINAHL, EMBASE, Cochrane Central Register of Controlled Trials, Scopus, and Web of Science from January 1, 2020 to September 29, 2023. We included studies that evaluated the heterologous vaccination strategy on immunocompromised individuals through outcomes related to COVID-19 (levels of anti-SARS-CoV-2 spike protein IgG, neutralizing antibodies, symptomatic COVID-19 infection, hospitalization, and death) in comparison to homologous schemes. We also used random-effect models to produce pooled odds ratio estimates. Heterogeneity was investigated with I estimation.
Eighteen studies met the inclusion criteria for this systematic review. Fourteen of them provided quantitative data for inclusion in the meta-analysis on vaccine response, being four of them also included in the vaccine effectiveness meta-analysis. The vaccination strategies (heterologous vs homologous) showed no difference in the odds of developing anti-SARS-CoV-2 spike protein IgG (odds ratio 1.12 [95% Cl: 0.73-1.72]). Heterologous schemes also showed no difference in the production of neutralizing antibodies (odds ratio 1.48 [95% Cl: 0.72-3.05]) nor vaccine effectiveness in comparison to homologous schemes (odds ratio 1.52 [95% CI: 0.66-3.53]).
Alternative heterologous COVID-19 vaccinations have shown equivalent antibody response rates and vaccine effectiveness to homologous schemes, potentially aiding global disparity of vaccine distribution.
我们评估了异源疫苗接种策略在免疫功能低下个体中针对新冠病毒感染结果的有效性,并将其与同源接种方法进行比较。
系统文献综述/荟萃分析。
我们检索了2020年1月1日至2023年9月29日期间的PubMed、CINAHL、EMBASE、Cochrane对照试验中央注册库、Scopus和科学网。我们纳入了通过与新冠病毒相关的结果(抗SARS-CoV-2刺突蛋白IgG水平、中和抗体、有症状的新冠病毒感染、住院和死亡)评估免疫功能低下个体异源疫苗接种策略并与同源方案进行比较的研究。我们还使用随机效应模型来生成合并比值比估计值。用I统计量研究异质性。
18项研究符合本系统综述的纳入标准。其中14项提供了纳入疫苗反应荟萃分析的定量数据,其中4项也纳入了疫苗有效性荟萃分析。疫苗接种策略(异源与同源)在产生抗SARS-CoV-2刺突蛋白IgG的几率上没有差异(比值比1.12 [95%置信区间:0.73 - 1.72])。与同源方案相比,异源方案在中和抗体产生方面也没有差异(比值比1.48 [95%置信区间:0.72 - 3.05]),在疫苗有效性方面也没有差异(比值比1.52 [95%置信区间:0.66 - 3.53])。
替代性异源新冠疫苗接种已显示出与同源方案相当的抗体反应率和疫苗有效性,这可能有助于缓解全球疫苗分配不均的问题。