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一剂维罗破伤风类毒素结合疫苗在孟加拉国儿童中的 5 年疫苗保护效果(TyVOID):一项整群随机试验。

5-year vaccine protection following a single dose of Vi-tetanus toxoid conjugate vaccine in Bangladeshi children (TyVOID): a cluster randomised trial.

机构信息

International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.

International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.

出版信息

Lancet. 2024 Oct 12;404(10461):1419-1429. doi: 10.1016/S0140-6736(24)01494-6.

Abstract

BACKGROUND

WHO currently recommends a single dose of typhoid conjugate vaccine (TCV) in high-burden countries based on 2-year vaccine efficacy data from large randomised controlled trials. Given the decay of immunogenicity, the protection beyond 2 years is unknown. We therefore extended the follow-up of the TyVAC trial in Bangladesh to assess waning of vaccine protection to 5 years after vaccination.

METHODS

We conducted a cluster randomised controlled trial (TyVAC; ISRCTN11643110) in Dhaka, Bangladesh, between 2018 and 2021. Children aged 9 months to 15 years were invited to receive a single dose of TCV or Japanese encephalitis vaccine between April 15, 2018, and November 16, 2019, based on the randomisation of their clusters of residence. Children who received the Japanese encephalitis vaccine were invited to receive TCV at the final visit between Jan 6, and Aug 31, 2021, according to the protocol. This follow-on study extended the follow-up of the original trial until Aug 14, 2023. The primary endpoint of this study was to compare the incidence of blood culture-confirmed typhoid between children who received TCV in 2018-19 (the previous-TCV group) and those who received the vaccine in 2021 (the recent-TCV group), to evaluate the relative decline in vaccine protection. We also did a nested study using the test-negative design comparing the recent-TCV and previous-TCV groups with unvaccinated individuals, as well as an immunogenicity study in a subset of 1500 children.

FINDINGS

Compared with the recent-TCV group, the previous-TCV group had an increased risk of typhoid fever between 2021-23, with an adjusted incidence rate ratio of 3·10 (95% CI 1·53 to 6·29; p<0·0001), indicating a decline in the protection of a single-dose of TCV 3-5 years after vaccination. The extrapolated vaccine effectiveness in years 3-5 was 50% (95% CI -13 to 78), and was validated using the test-negative design analysis, with a vaccine effectiveness of 84% (74 to 90) in the recent-TCV group and 55% (36 to 68) in the previous-TCV group, compared with unvaccinated individuals. Anti-Vi-IgG responses declined over the study period. The highest rate of decay was seen in children vaccinated at younger than 2 years in the original trial. The inverse correlation between age and the decay of antibodies was also seen in the subgroup analysis of vaccine effectiveness, where the youngest age group (<7 years at fever visits) exhibited the fastest waning, with vaccine effectiveness dropping to 24% (95% CI -29 to 55) at 3-5 years after vaccination.

INTERPRETATION

A decline in the protection conferred by a single-dose TCV was observed 3-5 years after vaccination, with the greatest decline in protection and immune responses observed in children vaccinated at younger ages. A booster dose of TCV around school entry age might be needed for children vaccinated while younger than 2 years to sustain protection against typhoid fever during the school years when the risk is the highest.

FUNDING

The Bill & Melinda Gates Foundation.

摘要

背景

世界卫生组织(WHO)目前根据大型随机对照试验提供的 2 年疫苗效力数据,建议在高负担国家使用伤寒结合疫苗(TCV)进行单剂接种。鉴于免疫原性衰减,其 2 年以上的保护效果尚不清楚。因此,我们延长了孟加拉国 TyVAC 试验的随访时间,以评估接种疫苗 5 年后疫苗保护效果的衰减情况。

方法

我们在孟加拉国达卡进行了一项群组随机对照试验(TyVAC;ISRCTN11643110),时间为 2018 年至 2021 年。2018 年 4 月 15 日至 2019 年 11 月 16 日,根据居住地群组的随机分组,邀请 9 个月至 15 岁的儿童接种 TCV 或日本脑炎疫苗。根据方案,2021 年 1 月 6 日至 8 月 31 日,接种日本脑炎疫苗的儿童受邀接种 TCV。这项后续研究将原始试验的随访时间延长至 2023 年 8 月 14 日。本研究的主要终点是比较 2018-19 年(前 TCV 组)和 2021 年(近期 TCV 组)接种 TCV 的儿童中血培养确诊伤寒的发病率,以评估疫苗保护效果的相对下降。我们还使用了一种巢式研究设计,使用了检测阴性设计,比较了近期 TCV 组和前 TCV 组与未接种疫苗的个体,以及在 1500 名儿童中进行了免疫原性研究。

结果

与近期 TCV 组相比,前 TCV 组在 2021-23 年间发生伤寒的风险增加,调整后的发病率比为 3.10(95%CI 1.53-6.29;p<0.0001),表明接种 TCV 3-5 年后疫苗保护效果下降。第 3-5 年的疫苗有效性外推值为 50%(95%CI -13 至 78),使用检测阴性设计分析进行验证,近期 TCV 组的疫苗有效性为 84%(74 至 90),前 TCV 组为 55%(36 至 68),与未接种疫苗的个体相比。抗-Vi-IgG 应答在研究期间呈下降趋势。在原始试验中,年龄越小接种疫苗的儿童抗体衰减速度最快。疫苗有效性的亚组分析也显示出年龄与抗体衰减之间的反比关系,在发热就诊时年龄最小的年龄组(<7 岁),疫苗有效性下降最快,在接种疫苗 3-5 年后降至 24%(95%CI -29 至 55)。

结论

接种 TCV 1 年后,疫苗保护效果出现下降,接种年龄越小的儿童,保护效果和免疫应答下降越明显。为了在学校期间(风险最高时)维持对伤寒的保护,可能需要在 2 岁以下接种疫苗的儿童在入学年龄左右接种 TCV 加强针。

资助

比尔及梅琳达·盖茨基金会。

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