Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
Department of Pediatrics, Ewha Womans University College of Medicine, Seoul, Republic of Korea; Center for Vaccine Evaluation and Study, Ewha Womans University College of Medicine, Seoul, Republic of Korea.
Vaccine. 2020 Dec 3;38(51):8145-8153. doi: 10.1016/j.vaccine.2020.10.085. Epub 2020 Nov 6.
Pneumococcal conjugate vaccines (PCVs) have been effective in reducing the disease burden caused by Streptococcus pneumoniae. The first licensed PCV (PCV7) was composed of capsular polysaccharides from seven serotypes. This was followed by PCV10, then PCV13, and currently there are a number of higher valency vaccines in development. As part of licensure, new vaccine iterations require assessment of immunogenicity. Since some antibodies can be non-functional, measuring functional antibodies is desirable. To meet this need, opsonophagocytic assays (OPAs) have been developed. Previous studies have shown there can be significant variations in OPA results from different laboratories. We have previously shown that standardizing OPA data using reference serum 007sp can decrease this variation. To extend this approach to additional serotypes, a panel of sera was tested by five laboratories using a multiplexed OPA for serotypes 2, 8, 9N, 10A, 11A, 12F, 15B, 17F, 20B, 22F, and 33F. Each sample was tested in five runs with 007sp tested three times in each run. Results were analyzed using a mixed effects ANOVA model. Standardization of the results significantly decreased the inter-laboratory variation for some serotypes. For serotypes 2, 8, and 11A, the variability was reduced by 40%, 45%, and 40%, respectively. For serotypes 12F, 17F, and 20B, the reductions were more modest (14%, 19%, and 24%, respectively). Standardization had little effect for the remaining serotypes. In many cases, the impact of normalization was blunted by the results from five sera that were collected after an extended post-vaccination interval. We have previously reported consensus values for 007sp for 13 serotypes, as well as the creation of a calibration serum panel ("Ewha Panel A"). Here, we report consensus values for 11 additional serotypes for 007sp and the creation of a second serum panel ("Ewha Panel B"). These consensus values will facilitate the development of next-generation PCVs.
肺炎球菌结合疫苗(PCV)在降低肺炎链球菌引起的疾病负担方面非常有效。第一种获得许可的 PCV(PCV7)由七种血清型的荚膜多糖组成。随后是 PCV10,然后是 PCV13,目前正在开发许多更高价的疫苗。作为许可的一部分,新的疫苗迭代需要评估其免疫原性。由于一些抗体可能没有功能,因此测量功能性抗体是可取的。为了满足这一需求,已经开发了调理吞噬测定(OPA)。以前的研究表明,不同实验室的 OPA 结果可能存在显著差异。我们之前已经表明,使用参考血清 007sp 标准化 OPA 数据可以减少这种变化。为了将这种方法扩展到其他血清型,我们使用针对血清型 2、8、9N、10A、11A、12F、15B、17F、20B、22F 和 33F 的多重 OPA 对一组血清进行了五个实验室的测试。每个样本在五个运行中进行测试,007sp 在每个运行中测试三次。使用混合效应方差分析模型对结果进行分析。结果标准化显著降低了一些血清型的实验室间变异性。对于血清型 2、8 和 11A,可变性分别降低了 40%、45%和 40%。对于血清型 12F、17F 和 20B,降低幅度较小(分别为 14%、19%和 24%)。对于其余的血清型,标准化几乎没有影响。在许多情况下,五个在延长疫苗接种后间隔时间收集的血清的结果削弱了归一化的影响。我们之前已经报告了针对 13 种血清型的 007sp 的共识值,以及创建了一个校准血清面板(“Ewha Panel A”)。在这里,我们报告了针对 007sp 的 11 种额外血清型的共识值以及创建了第二个血清面板(“Ewha Panel B”)。这些共识值将有助于开发下一代 PCV。