Development and Validation of an Efficient and Highly Sensitive Enzyme-Linked Immunosorbent Assay for Alemtuzumab Quantification in Human Serum and Plasma

被引:3
作者
Achini-Gutzwiller, Federica. R. [1 ,2 ,5 ]
van der Zijde, Cornelia. M. [1 ]
Jansen-Hoogendijk, Anja. M. [1 ]
Lankester, Arjan. C. [3 ]
Bredius, Robbert G. M. [3 ]
van Tol, Maarten J. D. [1 ]
Moes, Dirk Jan A. R. [4 ]
Schilham, Marco. W. [1 ]
机构
[1] Leiden Univ Med Ctr, Willem Alexander Childrens Hosp, Lab Paediat Immunol, Leiden, Netherlands
[2] Univ Childrens Hosp Zurich, Childrens Res Ctr CRC, Div Paediat Stem Cell Transplantat & Haematol, Zurich, Switzerland
[3] Leiden Univ Med Ctr, Willem Alexander Childrens Hosp, Dept Paediat, Leiden, Netherlands
[4] Leiden Univ Med Ctr, Dept Clin Pharm & Toxicol, Leiden, Netherlands
[5] Leiden Univ Med Ctr, Willem Alexander Childrens Hosp, Lab Paediat Immunol, Albinusdreef 2, NL-2333 ZA Leiden, Netherlands
关键词
alemtuzumab; anti-CD52 humanized monoclonal antibody; immunoassay; pharmacokinetics; CHRONIC LYMPHOCYTIC-LEUKEMIA; PHARMACOKINETICS; BLOOD; CAMPATH-1H; CD52;
D O I
10.1097/FTD.0000000000001037
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background:Alemtuzumab is a humanized monoclonal antibody that targets the CD52 glycoprotein expressed on most lymphocytes, subsequently inducing complement-mediated and antibody-mediated cytotoxicity. Owing to its ability to induce profound immune depletion, alemtuzumab is frequently used in patients before allogeneic hematopoietic stem cell transplantation to prevent graft rejection and acute graft-versus-host disease. In this clinical context, a stable immunoassay with high sensitivity and specificity to determine alemtuzumab levels is essential for performing pharmacokinetic and pharmacodynamic analyses; however, the available methods have several limitations. Here, we report the successful development and validation of an efficient and highly sensitive enzyme-linked immunosorbent assay technique based on commercially available reagents to quantify alemtuzumab in human serum or plasma.Methods:This enzyme-linked immunosorbent assay technique was developed and validated in accordance with the European Medicines Agency guidelines on bioanalytical method validation.Results:The assay sensitivity (lower limit of quantification) is 0.5 ng center dot mL(-1), and the dynamic range is 0.78-25 ng center dot mL(-1). To accommodate quantification of peak concentration and concentrations below the lympholytic level (<0.1 mcg center dot mL(-1)), patients' serum samples were prediluted 20-400 times according to the expected alemtuzumab concentration. The overall within-run accuracy was between 96% and 105%, whereas overall within-run precision (coefficient of variation) was between 3% and 9%. The between-run assessment provided an overall accuracy between 86% and 95% and an overall coefficient of variation between 5% and 14%.Conclusions:The developed assay provides accurate insight into alemtuzumab exposure and its effects on the clinical response to treatment, which is key to optimizing treatment strategies.
引用
收藏
页码:79 / 86
页数:8
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