Goldblatt D, Tan C Y, Burbidge P, McElhiney S, McLaughlin L, Tucker R, Rauh M, Sidhu M, Giardina P C
University College London Institute of Child Health, London, United Kingdom
Pfizer, Inc., Pearl River, New York, USA.
Clin Vaccine Immunol. 2015 Nov;22(11):1154-9. doi: 10.1128/CVI.00437-15. Epub 2015 Sep 9.
The pneumococcal enzyme-linked immunosorbent assay (ELISA) reference standard serum, lot 89SF, has been in use since 1990 and was replaced in 2013 with a new reference standard, 007sp, that is projected to be available for the next 25 years. 007sp was generated under an FDA-approved clinical protocol; 278 adult volunteers were immunized with the 23-valent unconjugated polysaccharide vaccine Pneumovax II, and a unit of blood was obtained twice from each immunized subject within 120 days following immunization. Pooled serum was prepared from the plasma of 262 subjects, filled at 6 ml per vial, and lyophilized. Five independent laboratories participated in bridging the serotype-specific IgG assignments for 89SF to the new reference standard, 007sp, to establish equivalent reference values for 13 pneumococcal capsular serotypes (1,3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, and 23F) by using the WHO reference ELISA. In a second study involving three laboratories, a similar protocol was used to assign weight-based IgG concentrations in micrograms per ml to 007sp of seven serotypes (8, 10A, 11A, 12F, 15B, 22F, and 33F) also present in the 23-valent pneumococcal unconjugated polysaccharide vaccine. In addition, the IgG assignments for a 12-member WHO quality control (QC) serum panel were also extended to cover these seven serotypes. Agreement was excellent, with a concordance correlation coefficient (r(c)) of >0.996 when each laboratory was compared to the assigned values for the 12 WHO QC serum samples. There are four remaining pneumococcal serotypes (2, 9N, 17F, and 20) found in Pneumovax II for which IgG assignments exist for 89SF and remain to be bridged.
肺炎球菌酶联免疫吸附测定(ELISA)参考标准血清,批号89SF,自1990年起使用,2013年被新的参考标准007sp取代,预计该标准将在未来25年内可用。007sp是根据美国食品药品监督管理局(FDA)批准的临床方案生成的;278名成年志愿者接种了23价非结合多糖疫苗肺炎球菌多糖疫苗II(Pneumovax II),并在免疫接种后的120天内从每个免疫接种对象身上采集两次血液样本。从262名受试者的血浆中制备混合血清,每瓶灌装6毫升,并进行冻干处理。五个独立实验室参与了将89SF的血清型特异性IgG赋值与新的参考标准007sp进行比对,通过使用世界卫生组织(WHO)参考ELISA为13种肺炎球菌荚膜血清型(1、3、4、5、6A、6B、7F、9V、14、18C、19A、19F和23F)建立等效参考值。在第二项涉及三个实验室的研究中,采用了类似的方案为23价肺炎球菌非结合多糖疫苗中也存在的七种血清型(8、10A、11A、12F、15B、22F和33F)的007sp赋予基于重量的每毫升微克IgG浓度。此外,一个由12个样本组成的WHO质量控制(QC)血清组的IgG赋值也扩展到涵盖这七种血清型。当将每个实验室与12个WHO QC血清样本的赋值进行比较时,一致性非常好,一致性相关系数(r(c))>0.996。肺炎球菌多糖疫苗II中还有四种剩余的肺炎球菌血清型(2、9N、17F和20),89SF对其有IgG赋值,仍有待进行比对。