Best practice recommendations for the transfer of cell-based assays for the measurement of neutralizing anti-drug antibodies

被引:0
|
作者
Belouski, Shelley S. [1 ,2 ]
Born, Danika [2 ]
Jacques, Susan [2 ]
Harder, Brandon [2 ,3 ]
Reynhardt, Kai [2 ,4 ]
Kaliyaperumal, Arunan [2 ]
Gupta, Shalini [2 ]
机构
[1] Xencor Inc, 111 W Lemon Ave,Floor 2, Monrovia, CA 91016 USA
[2] Amgen Inc, Thousand Oaks, CA 91320 USA
[3] Genentech Inc, Antibody Way, Oceanside, CA 92056 USA
[4] Reynhardt Consulting LLC, 2033 2nd Ave Apt 800, Seattle, WA 98121 USA
关键词
cell-based assays; immunogenicity; method validation and method transfer; neutralizing antibodies; LIGAND-BINDING ASSAYS; BIOLOGICAL THERAPEUTICS; OPTIMIZATION; VALIDATION; DESIGN; IMMUNOGENICITY;
D O I
10.4155/bio-2016-4998
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We recommend the application of a strategically designed step-wise approach to transfer cell-based assays that includes assessing analytical performance (through a fit for purpose validation and/or design of experiment robustness characterization), clinical performance (i.e., concordance) and performance or proficiency testing for long-term method monitoring. Here we focus on the application of this strategy to cell-based assays for the measurement of neutralizing anti-drug antibodies. This application is unique in that it requires a custom cell-based assay to be used over a long period of time (potentially phase 1a through the life of a marketed product) with the confidence of consistent method performance and result reporting. But, the process is adaptable to a variety of assay types and applications. We present lessons learned from two cell-based assay transfers that met relevant challenges while implementing alternative permutations of the recommended method transfer process.
引用
收藏
页码:1845 / 1857
页数:13
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