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GloBody Technology: Detecting Anti-Drug Antibody against VH/VL domains

The occurrence of anti-drug antibodies following administration of therapeutic monoclonal antibody to patients is a growing problem that is attracting attention from frontline clinicians. Ideally, an initial indicative point of care test would provide guidance to seek testing approved by the regulat...

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Autores principales: Saxena, Gauri K., Theocharopoulos, Ioannis, Aziz, Nisha Thaslima, Jones, Meleri, Gnanapavan, Sharmilee, Giovannoni, Gavin, Schmierer, Klaus, Garnett, James A., Baker, David, Kang, Angray S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002611/
https://www.ncbi.nlm.nih.gov/pubmed/32024871
http://dx.doi.org/10.1038/s41598-020-58041-3
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author Saxena, Gauri K.
Theocharopoulos, Ioannis
Aziz, Nisha Thaslima
Jones, Meleri
Gnanapavan, Sharmilee
Giovannoni, Gavin
Schmierer, Klaus
Garnett, James A.
Baker, David
Kang, Angray S.
author_facet Saxena, Gauri K.
Theocharopoulos, Ioannis
Aziz, Nisha Thaslima
Jones, Meleri
Gnanapavan, Sharmilee
Giovannoni, Gavin
Schmierer, Klaus
Garnett, James A.
Baker, David
Kang, Angray S.
author_sort Saxena, Gauri K.
collection PubMed
description The occurrence of anti-drug antibodies following administration of therapeutic monoclonal antibody to patients is a growing problem that is attracting attention from frontline clinicians. Ideally, an initial indicative point of care test would provide guidance to seek testing approved by the regulatory authorities. Here we describe a platform for the detection of IgG anti-drug antibodies that may provide an initial screen for all therapeutic monoclonal antibodies. Synthetic genes encoding Nanoluciferase polypeptides were inserted between the variable heavy and light domain encoding region of known antibody drugs (alemtuzumab and adalimumab) to generate recombinant single chain GloBodies, which retain the drug antibody paratopes and Nanoluciferase activity. In the presence of anti-drug antibodies, the GloBody is bound by specific IgG in the sample. These complexes are captured on immobilised Protein G and the luciferase activity determined. The amount of light generated being indicative of the anti-drug IgG antibody levels in serum. It should be possible to assemble GloBody reagents for all therapeutic monoclonal antibodies and adapt the capture phase to include additional specific isotypes. The assay has the potential to be developed for use with a drop of blood allowing initial pre-screening in a point of care setting.
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spelling pubmed-70026112020-02-14 GloBody Technology: Detecting Anti-Drug Antibody against VH/VL domains Saxena, Gauri K. Theocharopoulos, Ioannis Aziz, Nisha Thaslima Jones, Meleri Gnanapavan, Sharmilee Giovannoni, Gavin Schmierer, Klaus Garnett, James A. Baker, David Kang, Angray S. Sci Rep Article The occurrence of anti-drug antibodies following administration of therapeutic monoclonal antibody to patients is a growing problem that is attracting attention from frontline clinicians. Ideally, an initial indicative point of care test would provide guidance to seek testing approved by the regulatory authorities. Here we describe a platform for the detection of IgG anti-drug antibodies that may provide an initial screen for all therapeutic monoclonal antibodies. Synthetic genes encoding Nanoluciferase polypeptides were inserted between the variable heavy and light domain encoding region of known antibody drugs (alemtuzumab and adalimumab) to generate recombinant single chain GloBodies, which retain the drug antibody paratopes and Nanoluciferase activity. In the presence of anti-drug antibodies, the GloBody is bound by specific IgG in the sample. These complexes are captured on immobilised Protein G and the luciferase activity determined. The amount of light generated being indicative of the anti-drug IgG antibody levels in serum. It should be possible to assemble GloBody reagents for all therapeutic monoclonal antibodies and adapt the capture phase to include additional specific isotypes. The assay has the potential to be developed for use with a drop of blood allowing initial pre-screening in a point of care setting. Nature Publishing Group UK 2020-02-05 /pmc/articles/PMC7002611/ /pubmed/32024871 http://dx.doi.org/10.1038/s41598-020-58041-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Saxena, Gauri K.
Theocharopoulos, Ioannis
Aziz, Nisha Thaslima
Jones, Meleri
Gnanapavan, Sharmilee
Giovannoni, Gavin
Schmierer, Klaus
Garnett, James A.
Baker, David
Kang, Angray S.
GloBody Technology: Detecting Anti-Drug Antibody against VH/VL domains
title GloBody Technology: Detecting Anti-Drug Antibody against VH/VL domains
title_full GloBody Technology: Detecting Anti-Drug Antibody against VH/VL domains
title_fullStr GloBody Technology: Detecting Anti-Drug Antibody against VH/VL domains
title_full_unstemmed GloBody Technology: Detecting Anti-Drug Antibody against VH/VL domains
title_short GloBody Technology: Detecting Anti-Drug Antibody against VH/VL domains
title_sort globody technology: detecting anti-drug antibody against vh/vl domains
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002611/
https://www.ncbi.nlm.nih.gov/pubmed/32024871
http://dx.doi.org/10.1038/s41598-020-58041-3
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