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
相关论文
共 50 条
  • [21] Development of an enzyme-linked immunosorbent assay for the detection and quantification of the insecticide tebufenozide in wine
    Irwin, JA
    Tolhurst, R
    Jackson, P
    Gale, KR
    FOOD AND AGRICULTURAL IMMUNOLOGY, 2003, 15 (02) : 93 - 104
  • [22] Analytical validation of an enzyme-linked immunosorbent assay for the quantification of S100A12 in the serum and feces of cats
    Bridges, Cory S.
    Gruetzner, Niels
    Suchodolski, Jan S.
    Steiner, Joerg M.
    Heilmann, Romy M.
    VETERINARY CLINICAL PATHOLOGY, 2019, 48 (04) : 754 - 761
  • [23] Development of a sensitive enzyme-linked immunosorbent assay for eotaxin and measurement of its levels in human blood
    Morita, A
    Shimosako, K
    Kikuoka, S
    Taniguchi, Y
    Kitaura, M
    Sasakura, K
    Tamaki, M
    Tsuji, T
    Teraoka, H
    Yoshie, O
    Nakajima, T
    Hirai, K
    JOURNAL OF IMMUNOLOGICAL METHODS, 1999, 226 (1-2) : 159 - 167
  • [24] Development of a highly sensitive enzyme-linked immunosorbent assay for atrazine - Performance evaluation by flow injection immunoassay
    Gascon, J
    Oubina, A
    Ballesteros, B
    Barcelo, D
    Camps, F
    Marco, MP
    GonzalezMartinez, MA
    Morais, S
    Puchades, R
    Maquieira, A
    ANALYTICA CHIMICA ACTA, 1997, 347 (1-2) : 149 - 162
  • [25] Development of colorimetric enzyme-linked immunosorbent assay for human chorionic gonadotropin
    Prasad, PV
    Chaube, SK
    Shrivastav, TG
    Kumari, GL
    JOURNAL OF IMMUNOASSAY & IMMUNOCHEMISTRY, 2006, 27 (01) : 15 - 30
  • [26] A robust enzyme-linked immunosorbent assay to measure serum ramucirumab concentrations
    Desvignes, Celine
    Ternant, David
    Lecomte, Thierry
    Lievre, Astrid
    Ohresser, Marc
    Chautard, Romain
    Raoul, William
    Paintaud, Gilles
    BIOANALYSIS, 2021, 13 (07) : 565 - 574
  • [27] Development and validation of enzyme-linked Immunosorbent assays for quantification of anti-methotrexate IgG and fab in mouse and rat plasma
    Tayab, ZR
    Balthasar, JP
    JOURNAL OF IMMUNOASSAY & IMMUNOCHEMISTRY, 2004, 25 (04) : 335 - 344
  • [28] Development of an enzyme-linked immunosorbent assay for the determination of hexoestrol
    Xu, CL
    Peng, CF
    Liu, L
    Wang, L
    Jin, ZY
    Chu, XG
    JOURNAL OF ANIMAL AND FEED SCIENCES, 2006, 15 (01): : 159 - 171
  • [29] Development of an enzyme-linked immunosorbent assay for the detection of glyphosate
    Clegg, BS
    Stephenson, GR
    Hall, JC
    JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1999, 47 (12) : 5031 - 5037
  • [30] Development of an enzyme-linked immunosorbent assay for the insecticide thiamethoxam
    Kim, HJ
    Liu, SZ
    Keum, YS
    Li, QX
    JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2003, 51 (07) : 1823 - 1830