Department of Laboratory Medicine, the First Affiliated Hospital with Nanjing Medical University, Nanjing, Jiangsu, China.
Department of Pathology, the First Affiliated Hospital with Nanjing Medical University, Nanjing, Jiangsu, China.
JAMA Pediatr. 2021 Jul 1;175(7):e210347. doi: 10.1001/jamapediatrics.2021.0347. Epub 2021 Jul 6.
Rotavirus vaccines have been introduced worldwide, and the clinical association of different rotavirus vaccines with reduction in rotavirus gastroenteritis (RVGE) after introduction are noteworthy.
To evaluate the comparative benefit, risk, and immunogenicity of different rotavirus vaccines by synthesizing randomized clinical trials (RCTs) and observational studies.
Relevant studies published in 4 databases: Embase, PubMed, the Cochrane Library, and Web of Science were searched until July 1, 2020, using search terms including "rotavirus" and "vaccin*."
Randomized clinical trials and cohort and case-control studies involving more than 100 children younger than 5 years that reported the effectiveness, safety, or immunogenicity of rotavirus vaccines were included.
A random-effects model was used to calculate relative risks (RRs), odds ratios (ORs), risk differences, and 95% CIs. Adjusted indirect treatment comparison was performed to assess the differences in the protection of Rotarix and RotaTeq.
The primary outcomes were RVGE, severe RVGE, and RVGE hospitalization. Safety-associated outcomes involved serious adverse events, intussusception, and mortality.
A meta-analysis of 20 RCTs and 38 case-control studies revealed that Rotarix (RV1) significantly reduced RVGE (RR, 0.316 [95% CI, 0.224-0.345]) and RVGE hospitalization risk (OR, 0.347 [95% CI, 0.279-0.432]) among children fully vaccinated; RotaTeq (RV5) had similar outcomes (RVGE: RR, 0.350 [95% CI, 0.275-0.445]; RVGE hospitalization risk: OR, 0.272 [95% CI, 0.197-0.376]). Rotavirus vaccines also demonstrated higher protection against severe RVGE. Additionally, no significant differences in the protection of RV1 and RV5 against rotavirus disease were noted in adjusted indirect comparisons. Moderate associations were found between reduced RVGE risk and Rotavac (RR, 0.664 [95% CI, 0.548-0.804]), Rotasiil (RR, 0.705 [95% CI, 0.605-0.821]), and Lanzhou lamb rotavirus vaccine (RR, 0.407 [95% CI, 0.332-0.499]). All rotavirus vaccines demonstrated no risk of serious adverse events. A positive correlation was also found between immunogenicity and vaccine protection (eg, association of RVGE with RV1: coefficient, -1.599; adjusted R2, 99.7%).
The high protection and low risk of serious adverse events for rotavirus vaccines in children who were fully vaccinated emphasized the importance of worldwide introduction of rotavirus vaccination. Similar protection provided by Rotarix and RotaTeq relieves the pressure of vaccines selection for health care authorities.
轮状病毒疫苗已在全球范围内推出,不同轮状病毒疫苗在推出后与轮状病毒胃肠炎(RVGE)减少相关的临床关联值得关注。
通过综合随机临床试验(RCT)和观察性研究来评估不同轮状病毒疫苗的相对益处、风险和免疫原性。
在 4 个数据库中搜索了截至 2020 年 7 月 1 日发表的相关研究:Embase、PubMed、Cochrane 图书馆和 Web of Science,使用的搜索词包括“轮状病毒”和“疫苗”。
包括了超过 100 名年龄在 5 岁以下的儿童的 RCT 和队列及病例对照研究,这些研究报告了轮状病毒疫苗的有效性、安全性或免疫原性。
使用随机效应模型计算相对风险(RR)、优势比(OR)、风险差异和 95%置信区间。进行调整后的间接治疗比较,以评估 Rotarix 和 RotaTeq 保护作用的差异。
主要结局是 RVGE、严重 RVGE 和 RVGE 住院。与安全性相关的结局包括严重不良事件、肠套叠和死亡率。
对 20 项 RCT 和 38 项病例对照研究的荟萃分析显示,Rotarix(RV1)在完全接种疫苗的儿童中显著降低了 RVGE(RR,0.316[95%CI,0.224-0.345])和 RVGE 住院风险(OR,0.347[95%CI,0.279-0.432]);RotaTeq(RV5)也有类似的结果(RVGE:RR,0.350[95%CI,0.275-0.445];RVGE 住院风险:OR,0.272[95%CI,0.197-0.376])。轮状病毒疫苗也显示出对严重 RVGE 更高的保护作用。此外,在调整后的间接比较中,没有发现 RV1 和 RV5 对轮状病毒疾病的保护作用存在显著差异。中度关联表明,Rotavac(RR,0.664[95%CI,0.548-0.804])、Rotasiil(RR,0.705[95%CI,0.605-0.821])和兰州羔羊轮状病毒疫苗(RR,0.407[95%CI,0.332-0.499])对 RVGE 风险的降低有一定的保护作用。所有轮状病毒疫苗均未显示出严重不良事件的风险。免疫原性与疫苗保护作用之间也存在正相关(例如,与 RV1 的 RVGE:系数-1.599;调整后的 R2,99.7%)。
轮状病毒疫苗在完全接种疫苗的儿童中具有高保护作用和低严重不良事件风险,强调了在全球范围内推广轮状病毒疫苗接种的重要性。Rotarix 和 RotaTeq 提供的相似保护减轻了卫生保健当局在疫苗选择方面的压力。