Descriptive analysis of safety and immunogenicity profiles of a 15-valent pneumococcal conjugate vaccine between subcutaneous and intramuscular administration in a phase 1 study of healthy Japanese infants (V114-028).

IF 1.9 4区 医学 Q3 INFECTIOUS DISEASES Journal of Infection and Chemotherapy Pub Date : 2024-10-09 DOI:10.1016/j.jiac.2024.10.007
Keiko Wan, Masayoshi Shirakawa, Miyuki Sawata
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Abstract

Introduction: Subcutaneous (SC) administration is typically used for pediatric inactivated vaccines in Japan, whereas intramuscular (IM) administration is used outside Japan. We previously reported the safety and immunogenicity of V114, a 15-valent pneumococcal conjugate vaccine (PCV), administered subcutaneously and intramuscularly in a Japanese phase 1 study (V114-028). Here, we report secondary descriptive analyses on V114 groups of the study to further assess the safety and immunogenicity profiles of V114 between the administration routes.

Methods: A total of 133 healthy Japanese infants were randomized to receive V114-SC (n = 44), V114-IM (n = 45), or PCV13-SC (n = 44) at approximately 3, 4, 5, and 12-15 months of age. Adverse events (AEs) from Days 1-14 post-vaccination and vaccine-related serious AEs from Day 1 to 1-month post-dose 4 were reported. Serotype-specific immunoglobulin G (IgG) responses were measured across the vaccination series.

Results: Proportions of participants with solicited systemic AEs (irritability, somnolence, decreased appetite, and urticaria) and pyrexia were generally comparable between the groups. Compared with V114-SC, patients receiving V114-IM had a lower incidence of irritability and somnolence, and higher incidence of decreased appetite. Proportion of participants with solicited injection-site erythema was lower with V114-IM (82.2%) than V114-SC (100.0%). Those with other solicited injection-site AEs (induration, swelling, and pain) were generally comparable between the groups, with lower observed proportions with V114-IM. Serotype-specific IgG responses were also generally comparable between the groups, including at pre-toddler dose.

Conclusions: These results suggest the utility of IM administration as an option for V114 vaccination in Japanese infants.

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在一项针对日本健康婴儿的 1 期研究中,对皮下注射和肌肉注射 15 价肺炎球菌结合疫苗的安全性和免疫原性进行描述性分析 (V114-028)。
简介:在日本,小儿灭活疫苗通常采用皮下注射 (SC),而在日本以外则采用肌肉注射 (IM)。我们曾在日本的一项 1 期研究(V114-028)中报告了 15 价肺炎球菌结合疫苗 (PCV) V114 皮下注射和肌肉注射的安全性和免疫原性。在此,我们报告该研究中 V114 组的二次描述性分析,以进一步评估 V114 不同给药途径的安全性和免疫原性概况:共有 133 名健康的日本婴儿被随机分配到 V114-SC(44 人)、V114-IM(45 人)或 PCV13-SC(44 人)组,分别在婴儿约 3、4、5 和 12-15 个月大时给药。报告了接种后第 1-14 天的不良事件 (AE) 以及第 1 天至第 4 剂后 1 个月的疫苗相关严重不良事件。测量了整个接种系列的血清型特异性免疫球蛋白 G (IgG) 反应:结果:两组接种者出现全身性不良反应(烦躁、嗜睡、食欲下降和荨麻疹)和发热的比例基本相当。与V114-SC相比,接受V114-IM治疗的患者烦躁和嗜睡的发生率较低,食欲下降的发生率较高。V114-IM患者出现注射部位红斑的比例(82.2%)低于V114-SC(100.0%)。两组中出现其他注射部位AE(压痕、肿胀和疼痛)的人数基本相当,但V114-IM观察到的比例较低。各组之间的血清型特异性 IgG 反应(包括幼儿期前的剂量)也基本相当:这些结果表明,在日本婴儿接种 V114 疫苗时,IM 给药是一种有效的选择。
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来源期刊
Journal of Infection and Chemotherapy
Journal of Infection and Chemotherapy INFECTIOUS DISEASES-PHARMACOLOGY & PHARMACY
CiteScore
4.10
自引率
4.50%
发文量
303
审稿时长
47 days
期刊介绍: The Journal of Infection and Chemotherapy (JIC) — official journal of the Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases — welcomes original papers, laboratory or clinical, as well as case reports, notes, committee reports, surveillance and guidelines from all parts of the world on all aspects of chemotherapy, covering the pathogenesis, diagnosis, treatment, and control of infection, including treatment with anticancer drugs. Experimental studies on animal models and pharmacokinetics, and reports on epidemiology and clinical trials are particularly welcome.
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