National Influenza and Other Respiratory Viruses Center, Institut Pasteur de Dakar, Senegal.
Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, USA; Institute of Human Virology, University of Maryland School of Medicine, Baltimore, USA.
Vaccine. 2020 Nov 3;38(47):7526-7532. doi: 10.1016/j.vaccine.2020.09.059. Epub 2020 Oct 2.
Data on influenza vaccine immunogenicity in children are limited from tropical developing countries. We recently reported significant, moderate effectiveness of a trivalent inactivated influenza vaccine (IIV) in a controlled, cluster-randomized trial in children in rural Senegal during 2009, a year of H3N2 vaccine mismatch (NCT00893906). We report immunogenicity of IIV3 and inactivated polio vaccine (IPV) from that trial. We evaluated hemagglutination inhibition (HAI) and polio antibody titers in response to vaccination of three age groups (6 through 35 months, 3 through 5 years, and 6 through 8 years). As all children were IIV naïve, each received two vaccine doses, although titers were assessed after only the first dose for subjects aged 6 through 8 years. Seroconversion rates (4-fold titer rise or increase from <1:10 to ≥1:40) were 74-87% for A/H1N1, 76-87% for A/H3N2, and 54-79% for B/Yamagata. Seroprotection rates (HAI titer ≥ 1:40) were 79-88% for A/H1N1, 88-96% for A/H3N2, and 52-74% for B/Yamagata. IIV responses were lowest in the youngest age group, and they were comparable between ages 3 through 5 years after two doses and 6 through 8 years after one dose. We found that baseline seropositivity (HAI titer ≥ 1:10) was an effect modifier of IIV response. Using a seroprotective titer (HAI titer ≥ 1:160) recommended for IIV evaluation in children, we found that among subjects who were seropositive at baseline, 69% achieved seroprotection for both A/H1N1 and A/H3N2, while among those who were seronegative at baseline, seroprotection was achieved in 11% for A/H1N1 and 22% for A/H3N2. The IPV group had high baseline polio antibody seropositivity and appropriate responses to vaccination. Our data emphasize the importance of a two-dose IIV3 series in vaccine naïve children. IIV and IPV vaccines were immunogenic in Senegalese children.
有关流感疫苗在发展中国家的免疫原性的数据有限。我们最近报道了在塞内加尔农村进行的一项对照、整群随机试验中,三价灭活流感疫苗(IIV)在 2009 年具有显著的中度有效性,该年 H3N2 疫苗不匹配(NCT00893906)。我们报告了该试验中 IIV3 和灭活脊髓灰质炎疫苗(IPV)的免疫原性。我们评估了三个年龄组(6 至 35 个月、3 至 5 岁和 6 至 8 岁)接种后的血凝抑制(HAI)和脊髓灰质炎抗体滴度。由于所有儿童均为 IIV 初免者,他们均接受了两剂疫苗,但对于 6 至 8 岁的儿童,仅在第一剂后评估了滴度。甲型 H1N1、甲型 H3N2 和乙型 Yamagata 的血清转化率(4 倍滴度升高或从<1:10 增加至≥1:40)分别为 74-87%、76-87%和 54-79%。血清保护率(HAI 滴度≥1:40)分别为 79-88%、88-96%和 52-74%。年龄最小的年龄组的 IIV 反应最低,并且在接受两剂后 3 至 5 岁和接受一剂后 6 至 8 岁之间,年龄之间的反应相当。我们发现,基线血清阳性率(HAI 滴度≥1:10)是 IIV 反应的效应修饰因子。使用针对儿童 IIV 评估推荐的血清保护滴度(HAI 滴度≥1:160),我们发现,在基线时血清阳性的受试者中,69%的人对甲型 H1N1 和甲型 H3N2 均达到了血清保护,而在基线时血清阴性的受试者中,甲型 H1N1 的血清保护率为 11%,甲型 H3N2 的血清保护率为 22%。IPV 组基线脊髓灰质炎抗体血清阳性率较高,对疫苗接种有适当反应。我们的数据强调了对疫苗初免儿童进行两剂 IIV3 系列接种的重要性。IIV 和 IPV 疫苗在塞内加尔儿童中具有免疫原性。