Cargando…
Factor VIIIa-mimetic cofactor activity of a bispecific antibody to factors IX/IXa and X/Xa, emicizumab, depends on its ability to bridge the antigens
Emicizumab, a humanised bispecific antibody recognising factors (F) IX/IXa and X/Xa, can accelerate FIXa-catalysed FX activation by bridging FIXa and FX in a manner similar to FVIIIa. However, details of the emicizumab–antigen interactions have not been reported so far. In this study, we first showe...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Schattauer GmbH
2017
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292136/ https://www.ncbi.nlm.nih.gov/pubmed/28451690 http://dx.doi.org/10.1160/TH17-01-0030 |
_version_ | 1783380357417009152 |
---|---|
author | Kitazawa, Takehisa Esaki, Keiko Tachibana, Tatsuhiko Ishii, Shinya Soeda, Tetsuhiro Muto, Atsushi Kawabe, Yoshiki Igawa, Tomoyuki Tsunoda, Hiroyuki Nogami, Keiji Shima, Midori Hattori, Kunihiro |
author_facet | Kitazawa, Takehisa Esaki, Keiko Tachibana, Tatsuhiko Ishii, Shinya Soeda, Tetsuhiro Muto, Atsushi Kawabe, Yoshiki Igawa, Tomoyuki Tsunoda, Hiroyuki Nogami, Keiji Shima, Midori Hattori, Kunihiro |
author_sort | Kitazawa, Takehisa |
collection | PubMed |
description | Emicizumab, a humanised bispecific antibody recognising factors (F) IX/IXa and X/Xa, can accelerate FIXa-catalysed FX activation by bridging FIXa and FX in a manner similar to FVIIIa. However, details of the emicizumab–antigen interactions have not been reported so far. In this study, we first showed by surface plasmon resonance analysis that emicizumab bound FIX, FIXa, FX, and FXa with moderate affinities ( K (D) = 1.58, 1.52, 1.85, and 0.978 μM, respectively). We next showed by immunoblotting analysis that emicizumab recognised the antigens’ epidermal growth factor (EGF)-like domains. We then performed K (D) -based simulation of equilibrium states in plasma for quantitatively predicting the ways that emicizumab would interact with the antigens. The simulation predicted that only a small part of plasma FIX, FX, and emicizumab would form antigen-bridging FIX–emicizumab–FX ternary complex, of which concentration would form a bell-shaped relationship with emicizumab concentration. The bell-shaped concentration dependency was reproduced by plasma thrombin generation assays, suggesting that the plasma concentration of the ternary complex would correlate with emicizumab’s cofactor activity. The simulation also predicted that at 10.0–100 μg/ml of emicizumab–levels shown in a previous study to be clinically effective–the majority of plasma FIX, FX, and emicizumab would exist as monomers. In conclusion, emicizumab binds FIX/FIXa and FX/FXa with micromolar affinities at their EGF-like domains. The K (D) -based simulation predicted that the antigen-bridging ternary complex formed in circulating plasma would correlate with emicizumab’s cofactor activity, and the majority of FIX and FX would be free and available for other coagulation reactions. Institution where the work was carried out: Research Division, Chugai Pharmaceutical Co., Ltd. Supplementary Material to this article is available online at www.thrombosis-online.com. |
format | Online Article Text |
id | pubmed-6292136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Schattauer GmbH |
record_format | MEDLINE/PubMed |
spelling | pubmed-62921362018-12-13 Factor VIIIa-mimetic cofactor activity of a bispecific antibody to factors IX/IXa and X/Xa, emicizumab, depends on its ability to bridge the antigens Kitazawa, Takehisa Esaki, Keiko Tachibana, Tatsuhiko Ishii, Shinya Soeda, Tetsuhiro Muto, Atsushi Kawabe, Yoshiki Igawa, Tomoyuki Tsunoda, Hiroyuki Nogami, Keiji Shima, Midori Hattori, Kunihiro Thromb Haemost Emicizumab, a humanised bispecific antibody recognising factors (F) IX/IXa and X/Xa, can accelerate FIXa-catalysed FX activation by bridging FIXa and FX in a manner similar to FVIIIa. However, details of the emicizumab–antigen interactions have not been reported so far. In this study, we first showed by surface plasmon resonance analysis that emicizumab bound FIX, FIXa, FX, and FXa with moderate affinities ( K (D) = 1.58, 1.52, 1.85, and 0.978 μM, respectively). We next showed by immunoblotting analysis that emicizumab recognised the antigens’ epidermal growth factor (EGF)-like domains. We then performed K (D) -based simulation of equilibrium states in plasma for quantitatively predicting the ways that emicizumab would interact with the antigens. The simulation predicted that only a small part of plasma FIX, FX, and emicizumab would form antigen-bridging FIX–emicizumab–FX ternary complex, of which concentration would form a bell-shaped relationship with emicizumab concentration. The bell-shaped concentration dependency was reproduced by plasma thrombin generation assays, suggesting that the plasma concentration of the ternary complex would correlate with emicizumab’s cofactor activity. The simulation also predicted that at 10.0–100 μg/ml of emicizumab–levels shown in a previous study to be clinically effective–the majority of plasma FIX, FX, and emicizumab would exist as monomers. In conclusion, emicizumab binds FIX/FIXa and FX/FXa with micromolar affinities at their EGF-like domains. The K (D) -based simulation predicted that the antigen-bridging ternary complex formed in circulating plasma would correlate with emicizumab’s cofactor activity, and the majority of FIX and FX would be free and available for other coagulation reactions. Institution where the work was carried out: Research Division, Chugai Pharmaceutical Co., Ltd. Supplementary Material to this article is available online at www.thrombosis-online.com. Schattauer GmbH 2017-07 2017-11-28 /pmc/articles/PMC6292136/ /pubmed/28451690 http://dx.doi.org/10.1160/TH17-01-0030 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited. |
spellingShingle | Kitazawa, Takehisa Esaki, Keiko Tachibana, Tatsuhiko Ishii, Shinya Soeda, Tetsuhiro Muto, Atsushi Kawabe, Yoshiki Igawa, Tomoyuki Tsunoda, Hiroyuki Nogami, Keiji Shima, Midori Hattori, Kunihiro Factor VIIIa-mimetic cofactor activity of a bispecific antibody to factors IX/IXa and X/Xa, emicizumab, depends on its ability to bridge the antigens |
title | Factor VIIIa-mimetic cofactor activity of a bispecific antibody to factors IX/IXa and X/Xa, emicizumab, depends on its ability to bridge the antigens |
title_full | Factor VIIIa-mimetic cofactor activity of a bispecific antibody to factors IX/IXa and X/Xa, emicizumab, depends on its ability to bridge the antigens |
title_fullStr | Factor VIIIa-mimetic cofactor activity of a bispecific antibody to factors IX/IXa and X/Xa, emicizumab, depends on its ability to bridge the antigens |
title_full_unstemmed | Factor VIIIa-mimetic cofactor activity of a bispecific antibody to factors IX/IXa and X/Xa, emicizumab, depends on its ability to bridge the antigens |
title_short | Factor VIIIa-mimetic cofactor activity of a bispecific antibody to factors IX/IXa and X/Xa, emicizumab, depends on its ability to bridge the antigens |
title_sort | factor viiia-mimetic cofactor activity of a bispecific antibody to factors ix/ixa and x/xa, emicizumab, depends on its ability to bridge the antigens |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292136/ https://www.ncbi.nlm.nih.gov/pubmed/28451690 http://dx.doi.org/10.1160/TH17-01-0030 |
work_keys_str_mv | AT kitazawatakehisa factorviiiamimeticcofactoractivityofabispecificantibodytofactorsixixaandxxaemicizumabdependsonitsabilitytobridgetheantigens AT esakikeiko factorviiiamimeticcofactoractivityofabispecificantibodytofactorsixixaandxxaemicizumabdependsonitsabilitytobridgetheantigens AT tachibanatatsuhiko factorviiiamimeticcofactoractivityofabispecificantibodytofactorsixixaandxxaemicizumabdependsonitsabilitytobridgetheantigens AT ishiishinya factorviiiamimeticcofactoractivityofabispecificantibodytofactorsixixaandxxaemicizumabdependsonitsabilitytobridgetheantigens AT soedatetsuhiro factorviiiamimeticcofactoractivityofabispecificantibodytofactorsixixaandxxaemicizumabdependsonitsabilitytobridgetheantigens AT mutoatsushi factorviiiamimeticcofactoractivityofabispecificantibodytofactorsixixaandxxaemicizumabdependsonitsabilitytobridgetheantigens AT kawabeyoshiki factorviiiamimeticcofactoractivityofabispecificantibodytofactorsixixaandxxaemicizumabdependsonitsabilitytobridgetheantigens AT igawatomoyuki factorviiiamimeticcofactoractivityofabispecificantibodytofactorsixixaandxxaemicizumabdependsonitsabilitytobridgetheantigens AT tsunodahiroyuki factorviiiamimeticcofactoractivityofabispecificantibodytofactorsixixaandxxaemicizumabdependsonitsabilitytobridgetheantigens AT nogamikeiji factorviiiamimeticcofactoractivityofabispecificantibodytofactorsixixaandxxaemicizumabdependsonitsabilitytobridgetheantigens AT shimamidori factorviiiamimeticcofactoractivityofabispecificantibodytofactorsixixaandxxaemicizumabdependsonitsabilitytobridgetheantigens AT hattorikunihiro factorviiiamimeticcofactoractivityofabispecificantibodytofactorsixixaandxxaemicizumabdependsonitsabilitytobridgetheantigens |