Literature DB >> 33800950

Generation and Characterization of a Polyclonal Human Reference Antibody to Measure Anti-Drug Antibody Titers in Patients with Fabry Disease.

Malte Lenders1, David Scharnetzki1, Ali Heidari2, Daniele Di Iorio2, Seraphine Valeska Wegner2, Eva Brand1.   

Abstract

Male patients with Fabry disease (FD) are at high risk for the formation of antibodies to recombinant α-galactosidase A (AGAL), used for enzyme replacement therapy. Due to the rapid disease progression, the identification of patients at risk is highly warranted. However, currently suitable references and standardized protocols for anti-drug antibodies (ADA) determination do not exist. Here we generate a comprehensive patient-derived antibody mixture as a reference, allowing ELISA-based quantification of antibody titers from individual blood samples. Serum samples of 22 male patients with FD and ADAs against AGAL were pooled and purified by immune adsorption. ADA-affinities against agalsidase-α, agalsidase-β and Moss-AGAL were measured by quartz crystal microbalance with dissipation monitoring (QCM-D). AGAL-specific immune adsorption generated a polyclonal ADA mixture showing a concentration-dependent binding and inhibition of AGAL. Titers in raw sera and from purified total IgGs (r2 = 0.9063 and r2 = 0.8952, both p < 0.0001) correlated with the individual inhibitory capacities of ADAs. QCM-D measurements demonstrated comparable affinities of the reference antibody for agalsidase-α, agalsidase-β and Moss-AGAL (KD: 1.94 ± 0.11 µM, 2.46 ± 0.21 µM, and 1.33 ± 0.09 µM, respectively). The reference antibody allows the ELISA-based ADA titer determination and quantification of absolute concentrations. Furthermore, ADAs from patients with FD have comparable affinities to agalsidase-α, agalsidase-β and Moss-AGAL.

Entities:  

Keywords:  AGAL; ELISA; Fabry disease; affinities; anti-drug antibodies

Year:  2021        PMID: 33800950      PMCID: PMC7961705          DOI: 10.3390/ijms22052680

Source DB:  PubMed          Journal:  Int J Mol Sci        ISSN: 1422-0067            Impact factor:   5.923


  21 in total

1.  Safety and efficacy of recombinant human alpha-galactosidase A replacement therapy in Fabry's disease.

Authors:  C M Eng; N Guffon; W R Wilcox; D P Germain; P Lee; S Waldek; L Caplan; G E Linthorst; R J Desnick
Journal:  N Engl J Med       Date:  2001-07-05       Impact factor: 91.245

2.  Pharmacokinetics, pharmacodynamics, and safety of moss-aGalactosidase A in patients with Fabry disease.

Authors:  Julia B Hennermann; Laila Arash-Kaps; György Fekete; Andreas Schaaf; Andreas Busch; Thomas Frischmuth
Journal:  J Inherit Metab Dis       Date:  2019-02-11       Impact factor: 4.982

3.  Detailed epitope mapping of neutralizing anti-drug antibodies against recombinant α-galactosidase A in patients with Fabry disease.

Authors:  David Scharnetzki; Franciska Stappers; Malte Lenders; Eva Brand
Journal:  Mol Genet Metab       Date:  2020-08-28       Impact factor: 4.797

4.  Characterization of drug-neutralizing antibodies in patients with Fabry disease during infusion.

Authors:  Malte Lenders; Boris Schmitz; Stefan-Martin Brand; Dirk Foell; Eva Brand
Journal:  J Allergy Clin Immunol       Date:  2018-02-05       Impact factor: 10.793

5.  Effects of Orally Delivered Alpha-Galactosidase A on Gastrointestinal Symptoms in Patients With Fabry Disease.

Authors:  Malte Lenders; Michel Boutin; Christiane Auray-Blais; Eva Brand
Journal:  Gastroenterology       Date:  2020-06-12       Impact factor: 22.682

6.  Enzyme replacement therapy in Fabry disease: a randomized controlled trial.

Authors:  R Schiffmann; J B Kopp; H A Austin; S Sabnis; D F Moore; T Weibel; J E Balow; R O Brady
Journal:  JAMA       Date:  2001-06-06       Impact factor: 56.272

7.  Enzyme therapy for Fabry disease: neutralizing antibodies toward agalsidase alpha and beta.

Authors:  Gabor E Linthorst; Carla E M Hollak; Wilma E Donker-Koopman; Anneke Strijland; Johannes M F G Aerts
Journal:  Kidney Int       Date:  2004-10       Impact factor: 10.612

8.  Treatment of Fabry disease with different dosing regimens of agalsidase: effects on antibody formation and GL-3.

Authors:  Anouk C Vedder; Frank Breunig; Wilma E Donker-Koopman; Kevin Mills; Elisabeth Young; Bryan Winchester; Ineke J M Ten Berge; Johanna E M Groener; Johannes M F G Aerts; Christoph Wanner; Carla E M Hollak
Journal:  Mol Genet Metab       Date:  2008-04-18       Impact factor: 4.797

9.  Rapid Immunochromatographic Detection of Serum Anti-α-Galactosidase A Antibodies in Fabry Patients after Enzyme Replacement Therapy.

Authors:  Sachie Nakano; Takahiro Tsukimura; Tadayasu Togawa; Toya Ohashi; Masahisa Kobayashi; Katsuyoshi Takayama; Yukuharu Kobayashi; Hiroshi Abiko; Masatsugu Satou; Tohru Nakahata; David G Warnock; Hitoshi Sakuraba; Futoshi Shibasaki
Journal:  PLoS One       Date:  2015-06-17       Impact factor: 3.240

Review 10.  Anti-Drug Antibodies: Emerging Approaches to Predict, Reduce or Reverse Biotherapeutic Immunogenicity.

Authors:  Kathleen P Pratt
Journal:  Antibodies (Basel)       Date:  2018-05-31
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  2 in total

1.  Mechanisms of Neutralizing Anti-drug Antibody Formation and Clinical Relevance on Therapeutic Efficacy of Enzyme Replacement Therapies in Fabry Disease.

Authors:  Malte Lenders; Eva Brand
Journal:  Drugs       Date:  2021-11-08       Impact factor: 9.546

2.  Pre-existing anti-drug antibodies in Fabry disease show less affinity for pegunigalsidase alfa.

Authors:  Malte Lenders; Solvey Pollmann; Melina Terlinden; Eva Brand
Journal:  Mol Ther Methods Clin Dev       Date:  2022-07-31       Impact factor: 5.849

  2 in total

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