In vitro rescue of FGA deletion by lentiviral transduction of an afibrinogenemic patient's hepatocytes

J Thromb Haemost. 2014 Nov;12(11):1874-9. doi: 10.1111/jth.12714. Epub 2014 Oct 1.

Abstract

Background: Congenital afibrinogenemia is a rare inherited autosomal recessive disorder in which a mutation in one of three genes coding for the fibrinogen polypeptide chains Aα, Bβ and γ results in the absence of a functional coagulation protein. A patient with congenital afibrinogenemia, resulting from an FGA homozygous gene deletion, underwent an orthotopic liver transplant that resulted in complete restoration of normal hemostasis. The patient's explanted liver provided a unique opportunity to further investigate a potential novel treatment modality.

Objective: To explore a targeted gene therapy approach for patients with congenital afibrinogenemia.

Methods and results: At the time of transplant, the patient's FGA-deficient hepatocytes were isolated and transduced with lentiviral vectors encoding the human fibrinogen Aα-chain. FGA-transduced hepatocytes produced fully functional fibrinogen in vitro.

Conclusions: Orthotopic liver transplantation is a possible rescue treatment for failure of on-demand fibrinogen replacement therapy. In addition, we provide evidence that hepatocytes homozygous for a large FGA deletion can be genetically modified to restore Aα-chain protein expression and secrete a functional fibrinogen hexamer.

Keywords: congenital afibrinogenemia; fibrinogen Aalpha; genetic therapy; lentivirus; liver transplantation.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Afibrinogenemia / congenital*
  • Afibrinogenemia / diagnosis
  • Afibrinogenemia / genetics
  • Afibrinogenemia / metabolism
  • Afibrinogenemia / surgery
  • Cells, Cultured
  • Fibrinogen / biosynthesis
  • Fibrinogen / genetics*
  • Gene Deletion*
  • Gene Expression Regulation
  • Genetic Predisposition to Disease
  • Genetic Therapy / methods*
  • Genetic Vectors*
  • Hepatocytes / metabolism*
  • Homozygote
  • Humans
  • Lentivirus / genetics*
  • Liver Transplantation*
  • Male
  • Phenotype
  • Transduction, Genetic*

Substances

  • fibrinogen Aalpha
  • Fibrinogen