Maertens Kirsten, Burbidge Polly, Van Damme Pierre, Goldblatt David, Leuridan Elke
From the *Centre for the Evaluation of Vaccination, Vaccine and Infectious Diseases Institute, University of Antwerp, Antwerp, Belgium; and †Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.
Pediatr Infect Dis J. 2017 Dec;36(12):1186-1192. doi: 10.1097/INF.0000000000001601.
Maternal immunization with a tetanus, diphtheria and acellular pertussis (Tdap) vaccine may blunt infant pneumococcal immune responses after a primary series of vaccines.
As part of a prospective controlled cohort trial of Tdap (Boostrix; GSK Biologicals, Rixensart, Belgium) vaccination in pregnancy, infants born to vaccinated mothers and controls were immunized at 8 and 16 weeks and 12 months of age with 13-valent pneumococcal conjugate vaccine (Prevenar13; Pfizer, Wyeth, United States). Sera were tested for pneumococcal antibody concentrations against vaccine serotypes following primary and booster immunization.
Geometric mean concentration of antibodies to serotypes 1, 3, 4, 5, 6A, 7F, 9V, 14 and 19A was significantly lower after 2 doses of Prevenar13 vaccine in the offspring of the mothers vaccinated in pregnancy. This blunting effect disappeared after a booster dose at 12 months of age, except for serotypes 1 and 4. Despite this blunting, the percentage of children achieving the threshold of protection of 0.35 µg/mL was comparable in the vaccine and the control group both after primary and booster vaccination with only a significant lower rate of seroprotection in the vaccine group for serotype 3 after primary vaccination. After booster vaccination, seroprotection rates increased further for serotypes 3, 5, 6B, 9V and 23F.
The present results indicate a blunting effect after primary vaccination for some serotypes resolving after booster vaccination. Seroprotection rates were comparable both after primary and booster vaccination, except for serotype 3 with a significant lower seroprotection rate in the vaccine group after primary vaccination.
孕妇接种破伤风、白喉和无细胞百日咳(Tdap)疫苗可能会削弱婴儿在接种一系列主要疫苗后的肺炎球菌免疫反应。
作为孕期接种Tdap(博思rix;葛兰素史克生物制品公司,比利时里克森萨特)的前瞻性对照队列试验的一部分,接种疫苗的母亲所生婴儿和对照组婴儿在8周、16周和12月龄时接种13价肺炎球菌结合疫苗(沛儿13;辉瑞公司,惠氏,美国)。在初次免疫和加强免疫后检测血清中针对疫苗血清型的肺炎球菌抗体浓度。
孕期接种疫苗的母亲所生后代在接种2剂沛儿13疫苗后,针对血清型1、3、4、5、6A、7F、9V、14和19A的抗体几何平均浓度显著降低。这种削弱作用在12月龄加强免疫后消失,但血清型1和4除外。尽管有这种削弱作用,但在初次免疫和加强免疫后,疫苗组和对照组达到0.35μg/mL保护阈值的儿童百分比相当,仅在初次接种疫苗后疫苗组血清型3的血清保护率显著较低。加强免疫后,血清型3、5、6B、9V和23F的血清保护率进一步提高。
目前的结果表明,初次接种疫苗后对某些血清型有削弱作用,加强免疫后这种作用消失。初次免疫和加强免疫后的血清保护率相当,但血清型3除外,初次接种疫苗后疫苗组的血清保护率显著较低。