Immunogenicity of yellow fever vaccine co-administered with 13-valent pneumococcal conjugate vaccine in rural Gambia: A cluster-randomised trial

IF 4.5 3区 医学 Q2 IMMUNOLOGY Vaccine Pub Date : 2025-01-10 DOI:10.1016/j.vaccine.2025.126712
Isaac Osei , Jonas Schmidt-Chanasit , Paul V. Licciardi , Ousman Secka , Umberto D'Alessandro , Rasheed Salaudeen , Golam Sarwar , Ed Clarke , Nuredin I. Mohammed , Cattram Nguyen , Brian Greenwood , Stephanie Jansen , Grant A. Mackenzie
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Abstract

Introduction

Because booster doses of pneumococcal conjugate vaccine (PCV) may be given at a similar time to yellow fever vaccine (YF), it is important to assess the immune response to YF when co-administered with PCV. This has been investigated during a reduced-dose PCV trial in The Gambia.

Methods

In this phase 4, parallel-group, cluster-randomized trial, healthy infants aged 0–10 weeks were randomly allocated to receive either a two-dose schedule of PCV13 with a booster dose co-administered with YF vaccine at age 9 months (1 + 1 co-administration) or YF vaccine administered separately at age 10 months (1 + 1 separate) or the standard three early doses of PCV13 with YF vaccine at age 9 months (3 + 0 separate). Blood samples were collected 28–35 days post-vaccination and YF neutralizing antibody (NA) titres were measured. Proportions with seroprotective YF NA titres ≥ 1:8 were calculated with 95 % confidence intervals (CI). Non-inferiority was demonstrated if the lower limit of the CI for the difference in proportions between the co-administration and separate groups was greater than − 10 %.

Results

Forty-eight, 66, and 98 participants enrolled in 3 + 0 separate, 1 + 1 co-administration, and 1 + 1 separate groups respectively had NA results. Per protocol analysis of the 3 + 0 separate, 1 + 1 co-administration, 1 + 1 separate, and the combined 1 + 1 separate and 3 + 0 separate groups found that 81 %, 85 %, 92 %, and 88 % of participants respectively had YF NA titres ≥1:8. Results were similar with analysis by intention-to-treat. The difference in proportions comparing 1 + 1 co-administration and 1 + 1 separate groups was −7 % (95 % CI, −18 % to 3 %). The difference between 1 + 1 co-administration and 3 + 0 separate groups was 4 % (95 % CI, −10 % to 15 %). There was no statistical difference in the YF seroresponse when the YF vaccine was co-administered with PCV or administered separately.

Conclusions

No evidence was found of the non-inferiority of the seroresponse to YF vaccine when co-administered with PCV13. The levels of YF NA attaining seroprotection (NT ≥1:8) were high in all groups. PCV13 co-administered with YF vaccine at 9 months does not affect seroresponse to YF vaccine. http://www.isrctn.org/ - ISRCTN72821613.
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冈比亚农村地区黄热病疫苗与 13 价肺炎球菌结合疫苗联合接种的免疫原性:分组随机试验。
简介:由于肺炎球菌结合疫苗(PCV)的加强剂可能与黄热病疫苗(YF)同时接种,因此评估与PCV联合接种时对YF的免疫反应非常重要。在冈比亚进行的减少剂量PCV试验中对此进行了调查。方法:在这项4期平行组群随机试验中,0-10周龄的健康婴儿被随机分配,在9月龄时接受两剂PCV13加强剂与YF疫苗联合接种(1 + 1联合接种),或在10月龄时单独接种(1 + 1单独接种),或在9月龄时接受标准的三剂PCV13与YF疫苗联合接种(3 + 0单独接种)。接种后28 ~ 35 d采血,测定YF中和抗体(NA)滴度。计算血清YF NA滴度≥1:8的比例,95%置信区间(CI)。如果联合用药组和单独用药组之间比例差异的CI下限大于- 10%,则证明非劣效性。结果:3 + 0单独组、1 + 1联合组和1 + 1单独组分别有48例、66例和98例受试者有NA结果。对3 + 0单独用药、1 + 1联合用药、1 + 1单独用药以及1 + 1单独用药和3 + 0联合用药组的方案分析发现,分别有81%、85%、92%和88%的参与者的YF NA滴度≥1:8。结果与意向治疗分析相似。1 + 1联合用药组与1 + 1单独用药组的比例差异为- 7% (95% CI, - 18%至3%)。1 + 1联合用药组与3 + 0单独用药组的差异为4% (95% CI, - 10%至15%)。当YF疫苗与PCV联合接种或单独接种时,YF血清反应无统计学差异。结论:没有证据表明当与PCV13联合使用时,YF疫苗的血清反应是非劣效性的。各组获得血清保护(NT≥1:8)的YF NA水平均较高。9个月时PCV13与YF疫苗联合接种不影响对YF疫苗的血清反应。http://www.isrctn.org/ - ISRCTN72821613。
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来源期刊
Vaccine
Vaccine 医学-免疫学
CiteScore
8.70
自引率
5.50%
发文量
992
审稿时长
131 days
期刊介绍: Vaccine is unique in publishing the highest quality science across all disciplines relevant to the field of vaccinology - all original article submissions across basic and clinical research, vaccine manufacturing, history, public policy, behavioral science and ethics, social sciences, safety, and many other related areas are welcomed. The submission categories as given in the Guide for Authors indicate where we receive the most papers. Papers outside these major areas are also welcome and authors are encouraged to contact us with specific questions.
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