Centre Hospitalier Universitaire (CHU) de Québec-Université Laval Research Center, Quebec City, Quebec, Canada.
BC Children's Hospital Research Institute, Vaccine Evaluation Center, Vancouver, British Columbia, Canada; University of British Columbia, Department of Pediatrics, Vancouver, British Columbia, Canada.
Vaccine. 2023 Oct 26;41(45):6745-6753. doi: 10.1016/j.vaccine.2023.09.063. Epub 2023 Oct 8.
In 2019, the 3 + 1 schedule for children's vaccination (2-4-6-18 months old) was changed for a reduced 2 + 1 schedule (2-4-12 months old) in Quebec, Canada. We compared the post-booster anti-pertussis and anti-pneumococcus IgG antibody concentrations among children of Tdap-vaccinated and unvaccinated mothers for different vaccine schedules and vaccine formulations.
We conducted an observational cohort study. An invitation letter to potential participants was provided during a routine vaccination visit. Children's blood samples were analyzed post-booster at 13 (2 + 1 schedule) or 19 (3 + 1 schedule) months of age for antibodies against pertussis antigens (pertussis toxin (PT), filamentous hemagglutinin (FHA) and pertactin (PRN)) and pneumococcal antigens (serotypes 4, 18C, 19A, and 19F). IgG concentrations among children of Tdap-vaccinated and unvaccinated mothers for each vaccination schedule were compared using geometric mean concentrations (GMCs) and GMC ratios (GMRs), adjusting for potentially immune-response-influencing factors (aGMR). Serotype-specific pneumococcal seroprotection rates were also compared.
A total of 360 children were included for pertussis analysis and 248 for pneumococcal analysis. For the 2 + 1 schedule, 13-month-old children of Tdap-vaccinated mothers had lower GMCs against PT, FHA, and PRN, with aGMR (95 %CI) of 0.77 (0.65-0.90), 0.66 (0.55-0.79), 0.72 (0.52-0.99), respectively. For the 3 + 1 schedule, at 19 months old, the interference appeared to be attenuated (higher aGMR values). GMCs against PT were slightly higher in the 3 + 1 than the 2 + 1 schedule: 126.5 IU/ml vs 91.6 IU/ml; aGMR = 1.27. GMCs against PT, FHA and PRN were slightly higher among children who received Infanrix hexa® compared to those who received Pediacel® at 12 months old. For pneumococcal antibodies, at 13 months old, there was no strong evidence of immune interference in children of Tdap-vaccinated mothers.
Infant vaccination schedule may influence immune interference associated with maternal Tdap vaccination. More studies are needed to assess the clinical impact of this interference on children's protection.
2019 年,加拿大魁北克省将儿童疫苗接种的 3+1 时间表(2-4-6-18 个月龄)改为 2+1 时间表(2-4-12 个月龄)。我们比较了 Tdap 疫苗接种和未接种母亲的儿童在不同疫苗接种时间表和疫苗配方下的百日咳和肺炎球菌 IgG 抗体增强后浓度。
我们进行了一项观察性队列研究。在常规疫苗接种访问期间,向潜在参与者提供了一封邀请信。在 13 个月(2+1 时间表)或 19 个月(3+1 时间表)大时,对儿童的血液样本进行了百日咳抗原(百日咳毒素(PT)、丝状血凝素(FHA)和 pertactin(PRN))和肺炎球菌抗原(血清型 4、18C、19A 和 19F)的抗体分析。使用几何平均浓度(GMC)和 GMC 比值(GMR)比较 Tdap 疫苗接种和未接种母亲的儿童在每个疫苗接种时间表中的 IgG 浓度,并调整了潜在的免疫反应影响因素(aGMR)。还比较了血清型特异性肺炎球菌血清保护率。
共有 360 名儿童进行了百日咳分析,248 名儿童进行了肺炎球菌分析。对于 2+1 时间表,13 个月大的 Tdap 疫苗接种母亲的儿童对 PT、FHA 和 PRN 的 GMC 较低,调整潜在免疫反应影响因素后的 aGMR(95%CI)分别为 0.77(0.65-0.90)、0.66(0.55-0.79)、0.72(0.52-0.99)。对于 3+1 时间表,在 19 个月大时,这种干扰似乎减弱了(较高的 aGMR 值)。19 个月大时,3+1 时间表中 PT 的 GMC 略高于 2+1 时间表:126.5 IU/ml 比 91.6 IU/ml;aGMR=1.27。12 个月大时,与接种 Pediacel®的儿童相比,接种 Infanrix hexa®的儿童对 PT、FHA 和 PRN 的 GMC 略高。对于肺炎球菌抗体,在 13 个月大时,Tdap 疫苗接种母亲的儿童中没有强烈的免疫干扰证据。
婴儿疫苗接种时间表可能会影响与母体 Tdap 疫苗接种相关的免疫干扰。需要更多的研究来评估这种干扰对儿童保护的临床影响。