Recommendations for the design, optimization, and qualification of cell-based assays used for the detection of neutralizing antibody responses elicited to biological therapeutics

被引:164
作者
Gupta, Shalini [1 ]
Indelicato, Stephen R.
Jethwa, Vijay
Kawabata, Thomas
Kelley, Marian
Mire-Sluis, Anthony R.
Richards, Susan M.
Rup, Bonita
Shores, Elizabeth
Swanson, Steven J.
Wakshull, Eric
机构
[1] Amgen Inc, Thousand Oaks, CA 91320 USA
[2] Schering Plough Res Inst, Pharmsci Qual Qual Syst Improvement Off, Kenilworth, NJ 07033 USA
[3] Biogen Idec Inc, Res Triangle Pk, NC 27709 USA
[4] Pfizer Global Res & Dev, Groton, CT 06340 USA
[5] Centocor R&D Inc, Radnor, PA 19087 USA
[6] Genzyme Corp, Framingham, MA 01701 USA
[7] Wyeth Ayerst Res, Andover, MA 01810 USA
[8] Ctr Drug Evaluat & Res, Div Therapeut Prot, Off Biotechnol Prod, Bethesda, MD 20892 USA
[9] Biogen Idnc, Cambridge, MA 02142 USA
关键词
neutralizing antibody bioassay; cell-based assay; serum-based bioassay; immunogenicity assay; NAb assay; VALIDATION; ACTIVATION; RECEPTOR; EXPRESSION; GREEN; BETA;
D O I
10.1016/j.jim.2006.12.004
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The administration of biological therapeutics can evoke some level of immune response to the drug product in the receiving subjects. An immune response comprised of neutralizing antibodies can lead to loss of efficacy or potentially more serious clinical sequelae. Therefore, it is important to monitor the immunogenicity of biological therapeutics throughout the drug product development cycle. Immunoassays are typically used to screen for the presence and development of anti-drug product antibodies. However, in-vitro cell-based assays prove extremely useful for the characterization of immunoassay-positive samples to determine if the detected antibodies have neutralizing properties. This document provides scientific recommendations based on the experience of the authors for the development of cell-based assays for the detection of neutralizing antibodies in non-clinical and clinical studies. (c) 2006 Elsevier B.V. All rights reserved.
引用
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页码:1 / 18
页数:18
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