Siber George R, Chang Ih, Baker Sherryl, Fernsten Philip, O'Brien Katherine L, Santosham Mathuram, Klugman Keith P, Madhi Shabir A, Paradiso Peter, Kohberger Robert
Wyeth Vaccines Research, Pearl River, New York, USA.
Vaccine. 2007 May 10;25(19):3816-26. doi: 10.1016/j.vaccine.2007.01.119. Epub 2007 Feb 21.
Estimates of minimum protective antibody concentrations for vaccine preventable diseases are of critical importance in assessing whether new vaccines will be as effective as those for which clinical efficacy was shown directly. We describe a method for correlating pneumococcal anticapsular antibody responses of infants immunized with pneumococcal conjugate (PnC) vaccine (Prevenar) with clinical protection from invasive pneumococcal disease (IPD). Data from three double blind controlled trials in Northern Californian, American Indian and South African infants were pooled in a meta-analysis to derive a protective concentration of 0.35 microg/ml for anticapsular antibodies to the 7 serotypes in Prevenar. This concentration has been recommended by a WHO Working Group as applicable on a global basis for assessing the efficacy of future pneumococcal conjugate vaccines. The WHO Working Groups anticipated that modifications in antibody assays for pneumococcal anticapsular antibodies would occur. The principles for determining whether such assay modifications should change the protective concentration are outlined. These principles were applied to an improvement in the ELISA for anticapsular antibodies, i.e. absorption with 22F pneumococcal polysaccharide, which increases the specificity of the assay for vaccine serotype anticapsular antibodies by removing non-specific antibodies. Using sera from infants in the pivotal efficacy trial in Northern California Kaiser Permanente (NCKP), 22F absorption resulted in minimal declines in pneumococcal antibody in Prevenar immunized infants but significant declines in unimmunized controls. Recalculation of the protective concentration after 22F absorption resulted in only a small decline from 0.35 microg/ml to 0.32 microg/ml. These data support retaining the 0.35 microg/ml minimum protective concentration recommended by WHO for assessing the efficacy of pneumococcal conjugate vaccines in infants.
对于疫苗可预防疾病,估计最低保护性抗体浓度对于评估新疫苗是否会与那些已直接显示临床疗效的疫苗一样有效至关重要。我们描述了一种方法,用于将接种肺炎球菌结合疫苗(沛儿)的婴儿的肺炎球菌抗荚膜抗体反应与侵袭性肺炎球菌疾病(IPD)的临床保护相关联。来自北加利福尼亚、美国印第安人和南非婴儿的三项双盲对照试验的数据被汇总到一项荟萃分析中,得出沛儿中针对7种血清型的抗荚膜抗体的保护性浓度为0.35微克/毫升。一个世卫组织工作组已建议将该浓度在全球范围内用于评估未来肺炎球菌结合疫苗的效力。世卫组织工作组预计肺炎球菌抗荚膜抗体检测方法将会发生改变。概述了确定此类检测方法改变是否应改变保护性浓度的原则。这些原则被应用于抗荚膜抗体ELISA的改进,即使用22F肺炎球菌多糖进行吸收,通过去除非特异性抗体提高了该检测方法对疫苗血清型抗荚膜抗体的特异性。使用来自北加利福尼亚凯撒医疗集团(NCKP)关键效力试验中婴儿的血清,22F吸收导致接种沛儿的婴儿中肺炎球菌抗体的下降极小,但未接种的对照组中抗体显著下降。22F吸收后重新计算保护性浓度,结果仅从0.35微克/毫升小幅降至0.32微克/毫升。这些数据支持保留世卫组织推荐的0.35微克/毫升的最低保护性浓度,用于评估肺炎球菌结合疫苗对婴儿的效力。