Literature DB >> 35725847

Interference in a Neutralizing Antibody Assay for Odronextamab, a CD20xCD3 Bispecific mAb, from Prior Rituximab Therapy and Possible Mitigation Strategy.

Susan C Irvin1, Amanda D'Orvilliers2, Nicolin Bloch2, Kayla Boccio3, Jason Pennucci3,4, Jurriaan Brouwer-Visser5, Erica Ullman2, Manoj Rajadhyaksha6,7, Mohamed Hassanein6,8, Terra Potocky2,9, Albert Torri6, Aynur Hermann2, Michael A Partridge6.   

Abstract

A cell-based assay was developed to detect neutralizing anti-drug antibodies (NAbs) against odronextamab, a CD20xCD3 bispecific monoclonal antibody (mAb) under investigation for treatment of CD20+ B cell malignancies. In this assay, odronextamab bridges between two cell types, CD20-expressing HEK293 cells and CD3-expressing Jurkat T cells that generate a luciferase signal upon CD3 clustering. Patient samples containing NAbs directed to either arm of the bispecific drug block the odronextamab bridge formation between the cell lines thus preventing the generation of the luciferase signal. We determined that other anti-CD20 therapeutics also block bridge formation, resulting in false-positive results. In patient samples from odronextamab clinical trials, approximately 30% of baseline samples had a strong false-positive NAb signal that correlated with the presence of prior rituximab (anti-CD20) therapy. We determined that rituximab interference can be minimized by the addition of anti-rituximab antibodies in the NAb assay. Understanding and mitigating the impact of prior biologic exposure is increasingly important for implementing a successful bioanalytical strategy to support clinical drug development, especially in the immuno-oncology field. Odronextamab neutralizing antibody assay, interference, and mitigation. A Design of the odronextamab neutralizing antibody (NAb) assay where anti-CD20xCD3 drug bridges between CD20-expressing HEK293 cells and Jurkat T cells expressing an NFAT response element and luciferase reporter. True NAb prevents odronextamab from bridging between target and effector cells, thus preventing the expression of luciferase. B Interference with odronextamab from other anti-CD20 therapeutic antibodies (e.g., rituximab) from prior disease treatment generates a false-positive NAb result. Assay interference can be mitigated with an anti-idiotypic antibody against the interfering therapy.
© 2022. The Author(s).

Entities:  

Keywords:  bioanalytical; bispecific antibody; cell-based; immunogenicity; neutralizing antibodies

Mesh:

Substances:

Year:  2022        PMID: 35725847     DOI: 10.1208/s12248-022-00724-y

Source DB:  PubMed          Journal:  AAPS J        ISSN: 1550-7416            Impact factor:   3.603


  19 in total

1.  Haemoglobin interferes with the ex vivo luciferase luminescence assay: consequence for detection of luciferase reporter gene expression in vivo.

Authors:  M Colin; S Moritz; H Schneider; J Capeau; C Coutelle; M C Brahimi-Horn
Journal:  Gene Ther       Date:  2000-08       Impact factor: 5.250

2.  Pure red-cell aplasia and antierythropoietin antibodies in patients treated with recombinant erythropoietin.

Authors:  Nicole Casadevall; Joelle Nataf; Beatrice Viron; Amir Kolta; Jean-Jacques Kiladjian; Philippe Martin-Dupont; Patrick Michaud; Thomas Papo; Valerie Ugo; Irene Teyssandier; Bruno Varet; Patrick Mayeux
Journal:  N Engl J Med       Date:  2002-02-14       Impact factor: 91.245

Review 3.  How we manage follicular lymphoma.

Authors:  W Hiddemann; B D Cheson
Journal:  Leukemia       Date:  2014-02-28       Impact factor: 11.528

4.  Assessment of clinically relevant immunogenicity for mAbs; are we over reporting ADA?

Authors:  Mohamed Hassanein; Michael A Partridge; Weiping Shao; Albert Torri
Journal:  Bioanalysis       Date:  2020-09-18       Impact factor: 2.681

5.  Drug Removal Strategies in Competitive Ligand Binding Neutralizing Antibody (NAb) Assays: Highly Drug-Tolerant Methods and Interpreting Immunogenicity Data.

Authors:  Michael A Partridge; Elif Kabuloglu Karayusuf; Gary Shyu; Camille Georgaros; Albert Torri; Giane Sumner
Journal:  AAPS J       Date:  2020-08-17       Impact factor: 4.009

6.  The inter-heavy chain disulfide bonds of IgG4 are in equilibrium with intra-chain disulfide bonds.

Authors:  J Schuurman; G J Perdok; A D Gorter; R C Aalberse
Journal:  Mol Immunol       Date:  2001-01       Impact factor: 4.407

7.  Neutralizing antibodies to therapeutic enzymes: considerations for testing, prevention and treatment.

Authors:  Jinhai Wang; Jay Lozier; Gibbes Johnson; Susan Kirshner; Daniela Verthelyi; Anne Pariser; Elizabeth Shores; Amy Rosenberg
Journal:  Nat Biotechnol       Date:  2008-08       Impact factor: 54.908

8.  Obinutuzumab for the First-Line Treatment of Follicular Lymphoma.

Authors:  Robert Marcus; Andrew Davies; Kiyoshi Ando; Wolfram Klapper; Stephen Opat; Carolyn Owen; Elizabeth Phillips; Randeep Sangha; Rudolf Schlag; John F Seymour; William Townsend; Marek Trněný; Michael Wenger; Günter Fingerle-Rowson; Kaspar Rufibach; Tom Moore; Michael Herold; Wolfgang Hiddemann
Journal:  N Engl J Med       Date:  2017-10-05       Impact factor: 91.245

9.  A novel, native-format bispecific antibody triggering T-cell killing of B-cells is robustly active in mouse tumor models and cynomolgus monkeys.

Authors:  Eric J Smith; Kara Olson; Lauric J Haber; Bindu Varghese; Paurene Duramad; Andrew D Tustian; Adelekan Oyejide; Jessica R Kirshner; Lauren Canova; Jayanthi Menon; Jennifer Principio; Douglas MacDonald; Joel Kantrowitz; Nicholas Papadopoulos; Neil Stahl; George D Yancopoulos; Gavin Thurston; Samuel Davis
Journal:  Sci Rep       Date:  2015-12-11       Impact factor: 4.379

Review 10.  Understanding the Supersensitive Anti-Drug Antibody Assay: Unexpected High Anti-Drug Antibody Incidence and Its Clinical Relevance.

Authors:  Sam Song; Lili Yang; William L Trepicchio; Timothy Wyant
Journal:  J Immunol Res       Date:  2016-05-31       Impact factor: 4.818

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