Zasztowt-Sternicka Monika, Jagielska Anna, Rząd Michał, Szymusik Iwona, Hallmann Ewelina, Brydak Lidia, Nitsch-Osuch Aneta
Doctoral School, Medical University of Warsaw, Poland; Department of Social Medicine and Public Health, Medical University of Warsaw, Poland; 1(st) Chair and Department of Obstetrics and Gynecology, Medical University of Warsaw, Poland.
Doctoral School, Medical University of Warsaw, Poland.
Vaccine. 2025 Apr 19;53:127047. doi: 10.1016/j.vaccine.2025.127047. Epub 2025 Apr 8.
Infants and pregnant women are particularly vulnerable to severe illness and complications of influenza. It is necessary to increase knowledge about the safety and effectiveness of influenza vaccination during pregnancy to improve awareness among patients and healthcare professionals and increase to increase vaccination coverage.
A prospective, single-group clinical study was performed in the 2021/2022 and 2022/2023 seasons. The aim of the study was to assess the immunogenicity and tolerance of quadrivalent influenza vaccine (IIV4) in pregnant women, to evaluate transplacental antibody (AB) transfer after IIV4 administration, and to estimate optimal gestational age for vaccination. A group of 62 pregnant women between 14 and 37 weeks of gestation, including 59 mother-child pairs, underwent vaccination with IIV4. The humoral immune response was assessed using the EMA criteria.
Baseline seroprotection for all IIV4 strains was significantly correlated with previous vaccinations (p < .5). The postvaccination seroprotection ranged between 71 % and 94 %. A significant increase in AB titers was observed for all vaccine strains (p < .0000). No significant differences were observed in seroprotection and seroconversion rates or transplacental AB transfer between women vaccinated in the 2nd vs 3rd trimester of pregnancy. All IIV4 strains used in the study met at least 1 of the 3 EMA/CPMP immunogenicity criteria and may thus be considered immunogenic. Seroprotection for A/H1N1/pdm09, A/H3N2, B/lineage Victoria (B/V), and B/lineage Yamagata (B/Y) antigens was achieved by 97 %, 95 %, 59 %, and 85 % of neonates, respectively. Over 43 % of participants reported solicited injection site reactions. None of the participants reported severe or unsolicited adverse events.
IIV4 induced a strong immune response in pregnant women and a high rate of seroprotection in neonates. Immune protection in children did not differ according to the trimester of vaccination in pregnancy. IIV4 was well tolerated by pregnant women.
婴儿和孕妇特别容易患严重流感疾病及出现并发症。有必要增加关于孕期流感疫苗接种安全性和有效性的知识,以提高患者和医护人员的认识,并提高疫苗接种覆盖率。
在2021/2022和2022/2023季节进行了一项前瞻性单组临床研究。该研究的目的是评估四价流感疫苗(IIV4)在孕妇中的免疫原性和耐受性,评估IIV4接种后经胎盘抗体(AB)的转移情况,并估计最佳接种孕周。一组62名妊娠14至37周的孕妇,包括59对母婴,接受了IIV4接种。使用欧洲药品管理局(EMA)标准评估体液免疫反应。
所有IIV4毒株的基线血清保护率与既往接种情况显著相关(p < 0.5)。接种后血清保护率在71%至94%之间。所有疫苗毒株的AB滴度均显著升高(p < 0.0000)。在妊娠第二和第三孕期接种疫苗的女性之间,血清保护率、血清转化率或经胎盘AB转移率未观察到显著差异。研究中使用的所有IIV4毒株均至少符合EMA/人用药品委员会(CPMP)免疫原性标准中的1项,因此可被认为具有免疫原性。A/H1N1/pdm09、A/H3N2、B/维多利亚系(B/V)和B/山形系(B/Y)抗原的新生儿血清保护率分别为97%、95%、59%和85%。超过43%的参与者报告了接种部位的预期反应。没有参与者报告严重或非预期不良事件。
IIV4在孕妇中诱导了强烈的免疫反应,在新生儿中诱导了高血清保护率。儿童的免疫保护在孕期接种疫苗的不同孕周之间没有差异。IIV4在孕妇中耐受性良好。