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RTS,S/AS01 疟疾疫苗与麻疹、风疹和黄热病疫苗联合接种在加纳儿童中的免疫原性和安全性:一项 IIIb 期、多中心、非劣效性、随机、开放、对照试验。

Immunogenicity and safety of the RTS,S/AS01 malaria vaccine co-administered with measles, rubella and yellow fever vaccines in Ghanaian children: A phase IIIb, multi-center, non-inferiority, randomized, open, controlled trial.

机构信息

Kintampo Health Research Center, Ghana Health Service, PO Box 200, Kintampo, Ghana.

Kwame Nkrumah University of Science & Technology/Agogo Presbyterian Hospital, P.O. Box 27 Agogo, Asante Akyem, Ghana.

出版信息

Vaccine. 2020 Apr 16;38(18):3411-3421. doi: 10.1016/j.vaccine.2020.03.014. Epub 2020 Mar 17.

Abstract

BACKGROUND

To optimize vaccine implementation visits for young children, it could be efficient to administer the first RTS,S/AS01 malaria vaccine dose during the Expanded Programme on Immunization (EPI) visit at 6 months of age together with Vitamin A supplementation and the third RTS,S/AS01 dose on the same day as yellow fever (YF), measles and rubella vaccines at 9 months of age. We evaluated the safety and immunogenicity of RTS,S/AS01 when co-administered with YF and combined measles-rubella (MR) vaccines.

METHODS

In this phase 3b, open-label, controlled study (NCT02699099), 709 Ghanaian children were randomized (1:1:1) to receive RTS,S/AS01 at 6, 7.5 and 9 months of age, and YF and MR vaccines at 9 or 10.5 months of age (RTS,S coad and RTS,S alone groups, respectively). The third group received YF and MR vaccines at 9 months of age and will receive RTS,S/AS01 at 10.5, 11.5 and 12.5 months of age (Control group). All children received Vitamin A at 6 months of age. Non-inferiority of immune responses to the vaccine antigens was evaluated 1 month following co-administration versus RTS,S/AS01 or EPI vaccines (YF and MR vaccines) alone using pre-defined non-inferiority criteria. Safety was assessed until Study month 4.5.

RESULTS

Non-inferiority of antibody responses to the anti-circumsporozoite and anti-hepatitis B virus surface antigens when RTS,S/AS01 was co-administered with YF and MR vaccines versus RTS,S/AS01 alone was demonstrated. Non-inferiority of antibody responses to the measles, rubella, and YF antigens when RTS,S/AS01 was co-administered with YF and MR vaccines versus YF and MR vaccines alone was demonstrated. The safety profile of all vaccines was clinically acceptable in all groups.

CONCLUSIONS

RTS,S/AS01 can be co-administered with Vitamin A at 6 months and with YF and MR vaccines at 9 months of age during EPI visits, without immune response impairment to any vaccine antigen or negative safety effect.

摘要

背景

为了优化小儿疫苗接种计划,在扩大免疫规划(EPI)6 个月龄时接种第一剂 RTS,S/AS01 疟疾疫苗,同时给予维生素 A 补充剂,并在 9 个月龄时同时接种黄热病(YF)、麻疹和风疹(MR)疫苗,第三次接种 RTS,S/AS01 疫苗,可能会更有效。我们评估了 RTS,S/AS01 与 YF 和联合麻疹-风疹(MR)疫苗联合使用的安全性和免疫原性。

方法

在这项 3b 期、开放性标签、对照研究(NCT02699099)中,709 名加纳儿童按照 1:1:1 的比例随机分配(RTS,S 共接种和 RTS,S 单接种组,分别接受 6、7.5 和 9 个月龄的 RTS,S/AS01 疫苗接种,以及 9 或 10.5 个月龄的 YF 和 MR 疫苗接种)。第三组儿童在 9 个月龄时接种 YF 和 MR 疫苗,将在 10.5、11.5 和 12.5 个月龄时接种 RTS,S/AS01 疫苗(对照组)。所有儿童在 6 个月龄时均接受维生素 A 治疗。在联合使用与单独使用疫苗(YF 和 MR 疫苗)相比,1 个月后使用预先定义的非劣效性标准评估了疫苗抗原免疫应答的非劣效性。安全性评估直至研究第 4.5 个月。

结果

RTS,S/AS01 与 YF 和 MR 疫苗联合使用时,抗环子孢子蛋白和乙型肝炎表面抗原的抗体反应与 RTS,S/AS01 单用时相比,证明具有非劣效性。RTS,S/AS01 与 YF 和 MR 疫苗联合使用时,麻疹、风疹和 YF 抗原的抗体反应与 YF 和 MR 疫苗单用时相比,证明具有非劣效性。所有疫苗的安全性在所有组中均为临床可接受。

结论

在 EPI 访视期间,RTS,S/AS01 可以在 6 个月龄时与维生素 A 联合使用,在 9 个月龄时与 YF 和 MR 疫苗联合使用,不会影响任何疫苗抗原的免疫应答或产生不良的安全效应。

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