人类抗肺炎球菌标准参考血清中四种附加血清型的基于体重的抗体单位分配。

Q2 Biochemistry, Genetics and Molecular Biology Clinical and Vaccine Immunology Pub Date : 2017-09-05 Print Date: 2017-09-01 DOI:10.1128/CVI.00194-17
D Goldblatt, A McKeen, P Burbidge, S McElhiney, L McLaughlin, A Johnson, M Rauh, P C Giardina
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引用次数: 5

摘要

肺炎球菌酶联免疫吸附测定(ELISA)参比标准血清89SF号自1990年开始使用,并于2013年被新的参比标准血清007sp取代。该血清是根据fda批准的临床方案生成的,278名成年志愿者接种了23价非共轭多糖疫苗Pneumovax II,并在免疫后120天内获得两次一单位血液。从血浆中制备混合血清,每瓶充液6ml,并冻干。5个独立实验室参与了连接89SF与007sp血清型特异性IgG的工作,以建立13种肺炎球菌荚膜血清型(1、3、4、5、6A、6B、7F、9V、14、18C、19A、19F、23F)的等效参考值。随后的随访研究确定了另外7种血清型(8,10a, 11A, 12F, 15B, 22F, 33F)的等效参考值。在这项研究中,三个实验室对另外四种血清型(2,9n, 17F和20A)的007sp进行了以微克/毫升血清为单位的基于体重的IgG浓度测定。本研究完成了89SF到007sp的血清型分配。此外,世卫组织质量控制(QC)血清小组的12名成员的IgG抗体分配范围扩大,以涵盖另外四种血清型。一致性极好,当将每个实验室的值与12份WHO QC血清的指定值进行比较时,一致性相关系数(rc) >0.996。007sp制剂已取代89SF作为肺炎球菌参考标准。预计未来25年将有足够数量的007sp可供使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Assignment of Weight-Based Antibody Units for Four Additional Serotypes to a Human Antipneumococcal Standard Reference Serum, 007sp.

The pneumococcal enzyme-linked immunosorbent assay (ELISA) reference standard serum, lot 89SF, had been in use since 1990 and was replaced with a new reference standard serum, 007sp, in 2013. This serum was generated under an FDA-approved clinical protocol where 278 adult volunteers were immunized with the 23-valent unconjugated polysaccharide vaccine Pneumovax II and a unit of blood was obtained twice within 120 days following immunization. Pooled serum was prepared from the plasma, filled at 6 ml per vial, and lyophilized. Five independent laboratories participated in bridging the serotype-specific IgG assignments of 89SF to 007sp to establish equivalent reference values for 13 pneumococcal capsular serotypes (1, 3, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, 23F) using the WHO reference ELISA. A subsequent follow-up study established equivalent reference values for an additional seven serotypes (8, 10A, 11A, 12F, 15B, 22F, 33F). In this study, three laboratories assigned weight-based IgG concentrations in micrograms per milliliter of serum to 007sp for four additional serotypes: 2, 9N, 17F, and 20A. This study completes the assignment of serotypes for 89SF to 007sp. In addition, the IgG antibody assignments for a 12-member WHO quality control (QC) serum panel were extended to cover the four additional serotypes. Agreement was excellent, with a concordance correlation coefficient (rc ) of >0.996 when values from each laboratory were compared to the assigned values for the 12 WHO QC sera. The 007sp preparation has replaced 89SF as the pneumococcal reference standard. Sufficient quantities of 007sp are projected to be available for the next 25 years.

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来源期刊
Clinical and Vaccine Immunology
Clinical and Vaccine Immunology 医学-传染病学
CiteScore
2.88
自引率
0.00%
发文量
0
审稿时长
1.5 months
期刊介绍: Cessation. First launched as Clinical and Diagnostic Laboratory Immunology (CDLI) in 1994, CVI published articles that enhanced the understanding of the immune response in health and disease and after vaccination by showcasing discoveries in clinical, laboratory, and vaccine immunology. CVI was committed to advancing all aspects of vaccine research and immunization, including discovery of new vaccine antigens and vaccine design, development and evaluation of vaccines in animal models and in humans, characterization of immune responses and mechanisms of vaccine action, controlled challenge studies to assess vaccine efficacy, study of vaccine vectors, adjuvants, and immunomodulators, immune correlates of protection, and clinical trials.
期刊最新文献
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