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。

Vaccine Pub Date : 2025-02-15 Epub 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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引用次数: 0

摘要

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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunogenicity of yellow fever vaccine co-administered with 13-valent pneumococcal conjugate vaccine in rural Gambia: A cluster-randomised trial.

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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