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Modular Platform for the Development of Recombinant Hemoglobin Scavenger Biotherapeutics.
Buzzi, Raphael M; Owczarek, Catherine M; Akeret, Kevin; Tester, Andrea; Pereira, Natasha; Butcher, Rebecca; Brügger-Verdon, Valérie; Hardy, Matthew P; Illi, Marlies; Wassmer, Andreas; Vallelian, Florence; Humar, Rok; Hugelshofer, Michael; Buehler, Paul W; Gentinetta, Thomas; Schaer, Dominik J.
Afiliação
  • Buzzi RM; Division of Internal Medicine, Universitätsspital and University of Zurich, Zurich 8091, Switzerland.
  • Owczarek CM; CSL Limited, Bio21 Institute, Parkville, Victoria 3010, Australia.
  • Akeret K; Department of Neurosurgery, Clinical Neuroscience Center, Universitätsspital und University of Zurich, Zurich 8091, Switzerland.
  • Tester A; CSL Limited, Bio21 Institute, Parkville, Victoria 3010, Australia.
  • Pereira N; CSL Limited, Bio21 Institute, Parkville, Victoria 3010, Australia.
  • Butcher R; CSL Limited, Bio21 Institute, Parkville, Victoria 3010, Australia.
  • Brügger-Verdon V; Research and Development, CSL Behring AG, Bern 3014, Switzerland.
  • Hardy MP; CSL Limited, Bio21 Institute, Parkville, Victoria 3010, Australia.
  • Illi M; Research and Development, CSL Behring AG, Bern 3014, Switzerland.
  • Wassmer A; Research and Development, CSL Behring AG, Bern 3014, Switzerland.
  • Vallelian F; Division of Internal Medicine, Universitätsspital and University of Zurich, Zurich 8091, Switzerland.
  • Humar R; Division of Internal Medicine, Universitätsspital and University of Zurich, Zurich 8091, Switzerland.
  • Hugelshofer M; Department of Neurosurgery, Clinical Neuroscience Center, Universitätsspital und University of Zurich, Zurich 8091, Switzerland.
  • Buehler PW; Department of Pathology, The University of Maryland School of Medicine, Baltimore, Maryland 21201, United States.
  • Gentinetta T; The Center for Blood Oxygen Transport and Hemostasis, Department of Pediatrics, The University of Maryland School of Medicine, Baltimore, Maryland 21201, United States.
  • Schaer DJ; Research and Development, CSL Behring AG, Bern 3014, Switzerland.
Mol Pharm ; 18(8): 3158-3170, 2021 08 02.
Article em En | MEDLINE | ID: mdl-34292741
ABSTRACT
Cell-free hemoglobin (Hb) is a driver of disease progression in conditions with intravascular or localized hemolysis. Genetic and acquired anemias or emergency medical conditions such as aneurysmal subarachnoid hemorrhage involve tissue Hb exposure. Haptoglobin (Hp) captures Hb in an irreversible protein complex and prevents its pathophysiological contributions to vascular nitric oxide depletion and tissue oxidation. Preclinical proof-of-concept studies suggest that human plasma-derived Hp is a promising therapeutic candidate for several Hb-driven diseases. Optimizing the efficacy and safety of Hb-targeting biotherapeutics may require structural and functional modifications for specific indications. Improved Hp variants could be designed to achieve the desired tissue distribution, metabolism, and elimination to target hemolytic disease states effectively. However, it is critical to ensure that these modifications maintain the function of Hp. Using transient mammalian gene expression of Hp combined with co-transfection of the pro-haptoglobin processing protease C1r-LP, we established a platform for generating recombinant Hp-variants. We designed an Hpß-scaffold, which was expressed in this system at high levels as a monomeric unit (mini-Hp) while maintaining the key protective functions of Hp. We then used this Hpß-scaffold as the basis to develop an initial proof-of-concept Hp fusion protein using human serum albumin as the fusion partner. Next, a hemopexin-Hp fusion protein with bispecific heme and Hb detoxification capacity was generated. Further, we developed a Hb scavenger devoid of CD163 scavenger receptor binding. The functions of these proteins were then characterized for Hb and heme-binding, binding of the Hp-Hb complexes with the clearance receptor CD163, antioxidant properties, and vascular nitric oxide sparing capacity. Our platform is designed to support the generation of innovative Hb scavenger biotherapeutics with novel modes of action and potentially improved formulation characteristics, function, and pharmacokinetics.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Produtos Biológicos / Proteínas Recombinantes de Fusão / Haptoglobinas / Hemoglobinas / Hemopexina / Desenho de Fármacos Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Produtos Biológicos / Proteínas Recombinantes de Fusão / Haptoglobinas / Hemoglobinas / Hemopexina / Desenho de Fármacos Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article