a Department of Biostatistics and Computational Biology , University of Rochester Medical Center , Rochester , NY , USA.
b Center for Infectious Disease and Immunology , Rochester General Hospital Research Institute , Rochester , NY , USA.
Hum Vaccin Immunother. 2017 Oct 3;13(10):2316-2321. doi: 10.1080/21645515.2017.1329064.
Clinical trials of vaccines for children to prevent acute otitis media (AOM) infections caused by the bacteria Streptococcus pneumonia (Spn) are in Phase I. The objective of this study was to use serum antibody measurements to pneumococcal purified protein candidate antigens that occurred after natural "immunization" to predict a correlate of protection response needed following an injectable vaccine against AOM in children.
590 nasal and serum samples were collected from 129 healthy children at 6, 9, 12, 15, 18, 24 and 30-36 months of age and when the child developed AOM. Middle ear fluid to detect Spn was collected at every episode of AOM. Quantitative ELISA was used to determine serum IgG against 7 Spn vaccine antigens: PspA clade 3, PspA clade 5, PhtD, PhtE, LytB, PcpA and Ply. A correlate of protection (COP) was estimated by regressing AOM events against age adjusted antibody levels induced by nasopharyngeal colonization and AOM infections, using logistic regression and generalized estimating equation methods.
A significant COP was found for Spn PhtD (p = 0.0015), PhtE (p = 0.00034), LytB (p = 0.004), PcpA (p = 0.002), and Ply (p = 0.007) between higher antibody levels and reduced frequency of AOM. We estimated that a 2-fold higher antibody level in a child than the mean antibody level induced by NP colonization (after adjusting for subject age) to PhtD, LytB, PcpA, PhtE or Ply reduced the risk of AOM by 14-21%, a 4-fold higher level reduced it by 25-38% and a 10-fold higher level reduced it by 39-54%.
We developed a model to predict the necessary level of serum antibody and fold higher above a threshold to PhtD, PhtE, LytB, PcpA and Ply that would correlate with a reduced likelihood of AOM in children age 6-24 months old if enrolled in a Phase III clinical efficacy trial.
目前正在进行临床试验,以评估用于预防由肺炎链球菌(Spn)引起的儿童急性中耳炎(AOM)感染的疫苗。本研究的目的是使用血清抗体测量来预测对儿童 AOM 进行注射疫苗后的保护反应相关性,这种预测是基于对自然“免疫”后出现的肺炎球菌纯化蛋白候选抗原的研究。
129 名健康儿童在 6、9、12、15、18、24 个月和 30-36 个月时以及发生 AOM 时收集了 590 份鼻和血清样本。每次发生 AOM 时,均从中耳液中检测 Spn。采用定量 ELISA 法检测 7 种肺炎球菌疫苗抗原(PspA 第 3 族、PspA 第 5 族、PhtD、PhtE、LytB、PcpA 和 Ply)的血清 IgG 反应。使用逻辑回归和广义估计方程方法,通过回归鼻咽定植和 AOM 感染引起的年龄调整后的抗体水平来估计保护相关性(COP)。
Spn PhtD(p = 0.0015)、PhtE(p = 0.00034)、LytB(p = 0.004)、PcpA(p = 0.002)和 Ply(p = 0.007)抗体水平较高与 AOM 发生频率较低之间存在显著的 COP。我们估计,与 NP 定植(根据个体年龄调整)诱导的平均抗体水平相比,儿童体内的 PhtD、LytB、PcpA、PhtE 或 Ply 抗体水平高出 2 倍,患 AOM 的风险降低 14-21%;高出 4 倍,风险降低 25-38%;高出 10 倍,风险降低 39-54%。
我们建立了一个模型,以预测在 6-24 个月大的儿童中,如果参加 III 期临床试验,血清抗体水平和高于 PhtD、PhtE、LytB、PcpA 和 Ply 阈值的倍数,与 AOM 发生几率降低相关。