Vaccines, Medical and Scientific Affairs, International Developed Markets, Pfizer Ltd , Surrey , UK.
Vaccine Medical and Scientific Affairs, Pfizer Inc , Collegeville , PA , USA.
Hum Vaccin Immunother. 2019;15(10):2491-2500. doi: 10.1080/21645515.2019.1593082. Epub 2019 Apr 23.
Invasive meningococcal disease is rare and potentially devastating but often vaccine-preventable. Evaluation of meningococcal vaccine effectiveness is impractical owing to relatively low disease incidence; protection is therefore estimated using serum bactericidal antibody (SBA) assays. Original experiments on natural immunity established a titer of ≥4 as the correlate of protection for SBA assays using human complement (hSBA), but human complement is relatively difficult to obtain and standardize. Use of baby rabbit complement (rSBA assays), per standard guidelines for serogroups A and C, generally results in comparatively higher titers. Postlicensure effectiveness data for serogroup C conjugate vaccines support acceptance of rSBA titers ≥8 as the correlate of protection for this serogroup, but no thresholds have been formally established for serogroups A, W, and Y. Studies evaluating MenACWY-TT (Nimenrix®; Pfizer Inc, Sandwich, UK) immunogenicity have used both hSBA and rSBA assays, and ultimately suggest that rSBA may be more appropriate for these measurements.
侵袭性脑膜炎球菌病罕见且可能具毁灭性,但通常可通过疫苗预防。由于疾病发病率相对较低,评估脑膜炎球菌疫苗的有效性并不实际;因此,使用血清杀菌抗体(SBA)检测来估计保护作用。最初的天然免疫实验确定了 hSBA 检测中 ≥4 的滴度作为保护的相关因素,但是人补体相对难以获得和标准化。根据 A 群和 C 群的标准指南使用幼兔补体(rSBA 检测),通常会产生相对较高的滴度。C 群结合疫苗上市后的有效性数据支持接受 rSBA 滴度 ≥8 作为该血清型的保护相关因素,但尚未为 A、W 和 Y 群正式建立阈值。评估 MenACWY-TT(Nimenrix®;辉瑞公司,桑德林汉姆,英国)免疫原性的研究使用了 hSBA 和 rSBA 检测,最终表明 rSBA 可能更适合这些测量。