Research Center for Vitamins and Vaccines (CVIVA), Bandim Health Project, Statens Serum Institut, Artillerivej 5, 2300 Copenhagen S, Denmark.
Vaccine. 2012 Oct 19;30(47):6694-9. doi: 10.1016/j.vaccine.2012.08.055. Epub 2012 Sep 6.
WHO recommends oral polio vaccine at birth (OPV0) in polio endemic countries. During a period without OPV in Guinea-Bissau in 2004, we observed that not receiving OPV0 was associated with significantly decreased mortality in boys and better immune response to BCG vaccination. In 2007, whilst conducting a trial of BCG and vitamin A supplementation (VAS) at birth to low birthweight (LBW) children, OPV was again lacking for a short period. We used this natural experiment to test the previous observations.
In the trial LBW infants were randomised to early or delayed BCG and VAS or placebo at birth. We noted whether the children received OPV0 or not. We compared children who received No OPV0 with those who received OPV0 in the 2 months before and the 2 months after the period without OPV. Mortality was compared in Cox regression models providing adjusted hazard ratios (aHR); the immune response to BCG was assessed in Poisson models providing adjusted prevalence ratios (aPR).
Ninety-nine children received No OPV0 and were compared with 243 children who received OPV0. No OPV0 was associated with insignificantly higher mortality during the first year of life, the aHR being 1.83 (95% CI: 0.93-3.61). The effect was similar in boys and girls. Overall, there was no significant association between No OPV0 and having a positive PPD response (aPR=1.33 (0.64-2.78)) or a scar (aPR=1.02 (0.93-1.11)) after BCG vaccination, though No OPV0 boys were more likely to develop a scar (aPR: 1.10 (1.01-1.20)).
The findings did not support our previous observation that not receiving OPV0 was associated with reduced mortality in boys. The findings weakly supported that OPV0 leads to a dampened response to simultaneously administered BCG vaccine in boys.
世界卫生组织(WHO)建议在脊髓灰质炎流行国家为新生儿接种口服脊髓灰质炎疫苗(OPV0)。2004 年,几内亚比绍停止供应 OPV 期间,我们发现未接种 OPV0 的男孩死亡率显著降低,且对卡介苗(BCG)接种的免疫反应更好。2007 年,我们在低出生体重(LBW)儿童中开展了一项关于出生时接种卡介苗和维生素 A 补充剂(VAS)的试验,OPV 再次短暂缺乏。我们利用这一自然实验来检验之前的观察结果。
在该试验中,LBW 婴儿在出生时被随机分为早期或延迟接种 BCG 和 VAS 或安慰剂组。我们记录了儿童是否接种了 OPV0。我们将未接种 OPV0 的儿童与接种 OPV0 的儿童进行比较,比较对象为接种 OPV0 的儿童在无 OPV 期间前后 2 个月。使用 Cox 回归模型比较死亡率,提供调整后的风险比(aHR);使用 Poisson 模型评估对 BCG 的免疫反应,提供调整后的患病率比(aPR)。
99 名儿童未接种 OPV0,并与 243 名接种 OPV0 的儿童进行比较。在生命的第一年,未接种 OPV0 与死亡率略高相关,调整后的风险比为 1.83(95%CI:0.93-3.61)。男孩和女孩的结果相似。总体而言,未接种 OPV0 与 BCG 接种后出现阳性 PPD 反应(aPR=1.33(0.64-2.78))或疤痕(aPR=1.02(0.93-1.11))之间无显著关联,尽管未接种 OPV0 的男孩更有可能出现疤痕(aPR:1.10(1.01-1.20))。
研究结果不支持我们之前的观察结果,即未接种 OPV0 与男孩死亡率降低有关。研究结果微弱支持 OPV0 导致男孩同时接种的 BCG 疫苗免疫反应减弱。