Faculty of Health Sciences, University of Buea, Buea, Cameroon.
Health and Human Development (2HD) Research Network, Douala, Cameroon.
BMC Infect Dis. 2021 Dec 2;21(1):1205. doi: 10.1186/s12879-021-06913-y.
Hepatitis B virus (HBV) infection despite being a vaccine preventable disease remains a global public health problem. In Cameroon, the hepatitis B vaccine was introduced in the expanded program on immunisation in 2005, but there has been limited evaluation of the HBV surface antibody response post vaccination.
We investigated the immune response to hepatitis B vaccine in infants who received the DPT-Hep B-Hib vaccine, and we assessed HBsAg carriage in non-responders. We also investigated factors associated with non-response or poor response.
Using a hospital based cross sectional design and a structured questionnaire over a four-month period (January to April 2019), we collected data to determine factors associated with hepatitis B surface antibody (anti-HBs) response from infants aged 6 to 9 months attending infant welfare clinics (IWC) at the Buea and Limbe regional hospitals. We collected venous blood and measured anti-HBs titres using a quantitative Foresight® ELISA. We entered and analysed data using EpiData version 3.1 and SPSS version 25 respectively.
Of the 161 infants enrolled, 159 (98.8%) developed anti-HBs antibodies. Of these 159, 157 (97.5%) and 117 (72.7%) developed ≥ 10.0 mIU/ml (seroprotection) and ≥ 100.0 mIU/ml anti-HBs titres respectively. Being younger (6 months old) was associated with seroprotection (Cramer V = 0.322, p = 0.001). Spearman rho's relational analysis showed that immunity against HBV reduced as the duration since the last dose increased (r = -0.172; P = 0.029). However, a Firth logistic regression showed no significant association of factors with inadequate immunity. All 12 (7.5%) infants exposed to HBV at birth, received the hepatitis B vaccine at birth, including four who received HBIG, and all were protected. Four infants (2.5%) had anti-HBs titres < 10.0 mIU/mL (non-responders) but had no peculiarity.
The seroprotective rate following hepatitis B vaccination of infants is high even in exposed infants. Our study suggests that Cameroon's HBV vaccine in the Expanded Program on Immunisation (EPI) is effective against HBV, although we could not account for the 2.5% non-response rate. Large scale studies are needed to further explore non-response to the vaccine.
乙型肝炎病毒(HBV)感染虽然是一种可通过疫苗预防的疾病,但仍是一个全球性的公共卫生问题。在喀麦隆,乙型肝炎疫苗于 2005 年在扩大免疫规划中引入,但对疫苗接种后 HBV 表面抗体反应的评估有限。
我们调查了接受 DPT-Hep B-Hib 疫苗的婴儿对乙型肝炎疫苗的免疫反应,并评估了无应答者的 HBsAg 携带情况。我们还调查了与无应答或应答不良相关的因素。
使用基于医院的横断面设计和在四个月期间(2019 年 1 月至 4 月)的结构化问卷,我们收集了数据,以确定来自在布埃亚和利姆贝地区医院婴儿福利诊所就诊的 6 至 9 个月大的婴儿的乙型肝炎表面抗体(抗-HBs)反应的相关因素。我们采集了静脉血,并使用定量 Foresight®ELISA 测量抗-HBs 滴度。我们分别使用 EpiData 版本 3.1 和 SPSS 版本 25 输入和分析数据。
在纳入的 161 名婴儿中,159 名(98.8%)产生了抗-HBs 抗体。在这 159 名婴儿中,157 名(97.5%)和 117 名(72.7%)分别产生了≥10.0 mIU/ml(血清保护)和≥100.0 mIU/ml 的抗-HBs 滴度。年龄较小(6 个月)与血清保护有关(Cramer V=0.322,p=0.001)。Spearman rho 的关系分析显示,随着最后一剂疫苗接种时间的延长,对 HBV 的免疫力降低(r=-0.172;P=0.029)。然而,Firth 逻辑回归显示,没有发现因素与免疫不足有显著关联。所有 12 名(7.5%)在出生时接触过 HBV 的婴儿在出生时都接种了乙型肝炎疫苗,其中包括 4 名接受 HBIG 的婴儿,他们都受到了保护。有 4 名婴儿(2.5%)的抗-HBs 滴度<10.0 mIU/ml(无应答者),但没有特殊情况。
即使在暴露的婴儿中,婴儿接种乙型肝炎疫苗后的血清保护率也很高。我们的研究表明,喀麦隆扩大免疫规划中的乙型肝炎疫苗对 HBV 有效,尽管我们无法解释 2.5%的无应答率。需要进行大规模研究进一步探索对疫苗的无应答。