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ENPP1-Fc prevents mortality and vascular calcifications in rodent model of generalized arterial calcification of infancy

Author

Listed:
  • Ronald A. Albright

    (Yale University School of Medicine)

  • Paul Stabach

    (Yale University School of Medicine)

  • Wenxiang Cao

    (Yale University)

  • Dillon Kavanagh

    (Yale University School of Medicine)

  • Isabelle Mullen

    (Yale University School of Medicine)

  • Alexander A. Braddock

    (Yale University School of Medicine)

  • Mariel S. Covo

    (Yale University School of Medicine)

  • Martin Tehan

    (Yale University School of Medicine)

  • Guangxiao Yang

    (Yale University School of Medicine)

  • Zhiliang Cheng

    (Alexion)

  • Keith Bouchard

    (Alexion)

  • Zhao-Xue Yu

    (Alexion)

  • Stephanie Thorn

    (Yale University School of Medicine)

  • Xiangning Wang

    (Yale University School of Medicine)

  • Ewa J. Folta-Stogniew

    (WM Keck Biotechnology Research Laboratory, Yale University School of Medicine)

  • Alejandro Negrete

    (Biotechnology Core Laboratory, National Institute of Diabetes and Digestive Kidney Diseases, National Institutes of Health)

  • Albert J. Sinusas

    (Yale University School of Medicine)

  • Joseph Shiloach

    (Biotechnology Core Laboratory, National Institute of Diabetes and Digestive Kidney Diseases, National Institutes of Health)

  • George Zubal

    (Z-Concepts LLC)

  • Joseph A. Madri

    (Yale University School of Medicine)

  • Enrique M. De La Cruz

    (Yale University)

  • Demetrios T. Braddock

    (Yale University School of Medicine)

Abstract

Diseases of ectopic calcification of the vascular wall range from lethal orphan diseases such as generalized arterial calcification of infancy (GACI), to common diseases such as hardening of the arteries associated with aging and calciphylaxis of chronic kidney disease (CKD). GACI is a lethal orphan disease in which infants calcify the internal elastic lamina of their medium and large arteries and expire of cardiac failure as neonates, while calciphylaxis of CKD is a ubiquitous vascular calcification in patients with renal failure. Both disorders are characterized by vascular Mönckeburg’s sclerosis accompanied by decreased concentrations of plasma inorganic pyrophosphate (PPi). Here we demonstrate that subcutaneous administration of an ENPP1-Fc fusion protein prevents the mortality, vascular calcifications and sequela of disease in animal models of GACI, and is accompanied by a complete clinical and biomarker response. Our findings have implications for the treatment of rare and common diseases of ectopic vascular calcification.

Suggested Citation

  • Ronald A. Albright & Paul Stabach & Wenxiang Cao & Dillon Kavanagh & Isabelle Mullen & Alexander A. Braddock & Mariel S. Covo & Martin Tehan & Guangxiao Yang & Zhiliang Cheng & Keith Bouchard & Zhao-X, 2015. "ENPP1-Fc prevents mortality and vascular calcifications in rodent model of generalized arterial calcification of infancy," Nature Communications, Nature, vol. 6(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms10006
    DOI: 10.1038/ncomms10006
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    Cited by:

    1. Yuwen Li & Daniel Caballero & Julian Ponsetto & Alyssa Chen & Chuanlong Zhu & Jun Guo & Marie Demay & Harald Jüppner & Clemens Bergwitz, 2017. "Response of Npt2a knockout mice to dietary calcium and phosphorus," PLOS ONE, Public Library of Science, vol. 12(4), pages 1-16, April.

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