Literature DB >> 15475065

Alemtuzumab: validation of a sensitive and simple enzyme-linked immunosorbent assay.

Iman Jilani1, Michael Keating, Francis J Giles, Susan O'Brien, Hagop M Kantarjian, Maher Albitar.   

Abstract

Alemtuzumab (MabCampath) is a humanized rat monoclonal antibody that targets the CD52 antigen. It has been approved for the treatment of patients with resistant chronic lymphocytic leukaemia (CLL). Measuring plasma/serum levels of alemtuzumab is important for optimizing the dosing and scheduling of therapy; however, current assays in serum or plasma, based on the capture of alemtuzumab using CD52, are complicated and difficult to adapt for high throughput testing. We developed a simple sandwich enzyme-linked immunosorbent assay (ELISA) to measure alemtuzumab that takes advantage of the remaining rat sequence in alemtuzumab. Using specific anti-rat immunoglobulin (Ig) antibodies (absorbed against human Ig), alemtuzumab levels were measured in the serum and plasma of patients treated with alemtuzumab. Levels were similar between plasma and serum samples, in fresh samples and samples stored at 4 degrees C for 24 h, but were significantly lower in samples stored at room temperature for 24h. The assay was successfully used to determine serum alemtuzumab pre- and post-treatment. This assay is simple and adaptable for high throughput testing, with a limit of detection of 0.05 microg/ml and a coefficient of variation of +/-12.5%. No false positivity was observed in >200 samples tested. This validated assay should help optimize the dosing and scheduling of alemtuzumab therapy. The underlying principles are also applicable to the measurement of other humanized antibodies using an appropriate anti-Ig.

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Year:  2004        PMID: 15475065     DOI: 10.1016/j.leukres.2004.04.003

Source DB:  PubMed          Journal:  Leuk Res        ISSN: 0145-2126            Impact factor:   3.156


  4 in total

1.  Review of the Clinical Pharmacokinetics and Pharmacodynamics of Alemtuzumab and Its Use in Kidney Transplantation.

Authors:  Marieke van der Zwan; Carla C Baan; Teun van Gelder; Dennis A Hesselink
Journal:  Clin Pharmacokinet       Date:  2018-02       Impact factor: 6.447

2.  Preclinical pharmacology and toxicology evaluation of an anti-CD52 monoclonal antibody produced by perfusion fermentation process.

Authors:  Yanchao Wang; Chen Zheng; Chao Zhuang; Qiang Fu; Jinyan Qin; Baohong Zhang; Yanling Bian; Nianmin Qi; Jianwei Zhu
Journal:  J Ind Microbiol Biotechnol       Date:  2021-12-23       Impact factor: 4.258

3.  A general process for the development of peptide-based immunoassays for monoclonal antibodies.

Authors:  Ana B Sanchez; Tammy Nguyen; Rhanika Dema-Ala; Andrew C Kummel; Thomas J Kipps; Bradley T Messmer
Journal:  Cancer Chemother Pharmacol       Date:  2010-01-20       Impact factor: 3.333

4.  Generation of anti-idiotype scFv for pharmacokinetic measurement in lymphoma patients treated with chimera anti-CD22 antibody SM03.

Authors:  Qi Zhao; Pui-Fan Wong; Susanna S T Lee; Shui-On Leung; Wing-Tai Cheung; Jun-Zhi Wang
Journal:  PLoS One       Date:  2014-05-09       Impact factor: 3.240

  4 in total

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