Huang Lili, Yang Xinyi, Li Hong, Xie Zhiqiang, Zhu Taotao, You Wangyang, Wang Zeng, Tan Jiebing, Feng Guangwei, Sun Qingmin, Wang Bin, Han Xing, Wang Yanxia
Vaccine Clinical Research Center, Henan Provincial Center for Disease Control and Prevention, Zhengzhou, China.
Clinical Research and Development Center, Sinovac Life Sciences Co., Ltd, Beijing, China.
Hum Vaccin Immunother. 2025 Dec;21(1):2517489. doi: 10.1080/21645515.2025.2517489. Epub 2025 Jun 19.
In a previous phase 3 clinical trial, a 23-valent pneumococcal polysaccharide vaccine (PPV23) induced robust immune responses in participants aged 2 years and older. We conducted this study to evaluate the immune persistence of a single dose of PPV23 6 years after vaccination. In this follow-up study, 600 participants aged 2 years and older (referred to the age of vaccination) who had received a single dose of either test vaccine or control vaccine in the previous clinical trial were enrolled in a 3:1 ratio. Blood samples were collected to determine anti-capsular immunoglobulin G (IgG) antibody levels against 23 serotypes with enzyme-linked immunosorbent assay (ELISA). A total of 598 subjects were included for immune persistence analysis. Six years after vaccination, the geometric mean concentrations (GMCs) of IgG antibodies to most serotypes remained higher than prior to vaccination in both groups (1.1-1.8 folds vs.1.1-1.7 folds), although there was a significant decrease compared to 28 days. The results suggested PPV23 could provide protection 6 years after vaccination. Considering the significant decrease of antibody level, the revaccination in high-risk population may be needed. ClinicalTrial.gov identifier: NCT03480763.
在之前的一项3期临床试验中,23价肺炎球菌多糖疫苗(PPV23)在2岁及以上的参与者中诱导了强烈的免疫反应。我们开展本研究以评估接种PPV23单剂6年后的免疫持久性。在这项随访研究中,按照3:1的比例纳入了600名2岁及以上(以接种时年龄为准)的参与者,这些参与者在之前的临床试验中接种了单剂试验疫苗或对照疫苗。采集血样,采用酶联免疫吸附测定(ELISA)法测定针对23种血清型的抗荚膜免疫球蛋白G(IgG)抗体水平。共有598名受试者纳入免疫持久性分析。接种疫苗6年后,两组中针对大多数血清型的IgG抗体几何平均浓度(GMC)均高于接种前(分别为1.1 - 1.8倍和1.1 - 1.7倍),尽管与接种后28天相比有显著下降。结果表明PPV23在接种疫苗6年后仍可提供保护。考虑到抗体水平显著下降,可能需要对高危人群进行再次接种。ClinicalTrial.gov标识符:NCT03480763。