Ma Q L, Zhang M, Liu L J, Zhou Y, Yuan W, Yang M, Liu S X, Luo L Y, Chen H P, Xiao Y H, Qi Q, Yang X M
Sichuan Provincial Center for Disease Control and Prevention, Chengdu 610041, China.
China National Biotech Group Company Limited, Beijing 100024, China.
Zhonghua Liu Xing Bing Xue Za Zhi. 2023 Jul 10;44(7):1119-1125. doi: 10.3760/cma.j.cn112338-20221130-01019.
To evaluate the immunogenicity and safety of revaccination of 23-valent pneumococcal polysaccharide vaccine (PPV23) in elderly people aged ≥60 years. The elderly aged ≥60 years with 1 dose of PPV23 vaccination were selected as revaccination group and those without history of pneumococcal vaccine immunization were selected as the first vaccination group. One dose of PPV23 was administered to both groups, and the first blood samples were collected before vaccination while the second blood samples were collected on day 28-40 after vaccination. ELISA was used to detect the concentrations of anti-specific serotype Streptococcus pneumoniae podocyte polysaccharide immunoglobulin G, and the safety of the vaccination was evaluated after 30 days. The geometric mean concentration (GMC) of antibody to 23 serotypes before the vaccination (0.73-13.73 μg/ml) was higher in revaccination group than in the first vaccination group (0.39-7.53 μg/ml), the GMC after the vaccination (1.42-31.65 μg/ml) was higher than that before the vaccination (0.73-13.73 μg/ml) in the revaccination group, and the GMC after the vaccination (1.62-43.76 μg/ml) was higher than that before the vaccination (0.39-7.53 μg/ml) in the first vaccination group; the geometric mean growth multiple in revaccination group (2.16-3.60) was lower than that in the first vaccination group (3.86-16.13); The mean 2-fold antibody growth rate was lower in revaccination group (53.68%, 95%: 52.30%-55.06%) than in the first vaccination group (93.16%, 95%: 92.18%- 94.15%), all differences were significant (<0.001). After the vaccination, 13 serotypes of GMC were higher in the first vaccination group than in revaccination group (<0.001), the differences were not significant for 10 serotypes of GMC (>0.05). The incidence of local adverse reaction was 19.20% and 13.27% in revaccination group and the first vaccination group, respectively (=0.174). The antibody level in ≥60 years people who received one dose of PPV23 after a 5-year interval was still higher than that in unvaccinated people. The antibody level decreased after 5 years of the first vaccination, and the antibody level could be rapidly increased by one more dose vaccination, but the overall immune response was lower than that of the first vaccination; revaccination with PPV23 has a good safety.
评估23价肺炎球菌多糖疫苗(PPV23)对≥60岁老年人进行再接种的免疫原性和安全性。将接种过1剂PPV23的≥60岁老年人选为再接种组,将无肺炎球菌疫苗免疫史的老年人选为首次接种组。两组均接种1剂PPV23,首次血样在接种前采集,第二次血样在接种后28 - 40天采集。采用ELISA法检测抗特异性血清型肺炎链球菌荚膜多糖免疫球蛋白G的浓度,并在接种30天后评估接种安全性。再接种组接种前23种血清型抗体的几何平均浓度(GMC)(0.73 - 13.73μg/ml)高于首次接种组(0.39 - 7.53μg/ml),再接种组接种后GMC(1.42 - 31.65μg/ml)高于接种前(0.73 - 13.73μg/ml),首次接种组接种后GMC(1.62 - 43.76μg/ml)高于接种前(0.39 - 7.53μg/ml);再接种组几何平均增长倍数(2.16 - 3.60)低于首次接种组(3.86 - 16.13);再接种组平均2倍抗体增长率(53.68%,95%:52.30% - 55.06%)低于首次接种组(93.16%,95%:92.18% - 94.15%),差异均有统计学意义(<0.001)。接种后,首次接种组13种血清型的GMC高于再接种组(<0.001),10种血清型的GMC差异无统计学意义(>0.05)。再接种组和首次接种组局部不良反应发生率分别为19.20%和13.27%(P = 0.174)。间隔5年后接种1剂PPV23的≥60岁人群抗体水平仍高于未接种人群。首次接种5年后抗体水平下降,再次接种1剂可使抗体水平迅速升高,但总体免疫反应低于首次接种;PPV23再接种具有良好的安全性。