Alpha-1 antitrypsin augmentation therapy. Review uri icon

Overview

MeSH

  • Evidence-Based Medicine
  • Humans
  • Registries

MeSH Major

  • Serine Proteinase Inhibitors
  • alpha 1-Antitrypsin
  • alpha 1-Antitrypsin Deficiency

abstract

  • The therapy of alpha-1 antitrypsin deficiency (AATD) is an example of a medical triumph over a common hereditary disease. Based on the understanding of the pathogens of the disease as a deficiency in liver production of alpha-1 antitrypsin (AAT) resulting from inherited genetic variation in both parental AAT genes, the knowledge that A1AT functions primarily to inhibit neutrophil elastase (NE), and the observation that NE instilled into the lung of experimental animals resulted in emphysema, the concept evolved that the pulmonary manifestations of the disease could be halted by intermittent intravenous infusions of AAT purified from pooled human plasma. Following preliminary clinical studies in the academic community, and then pharmaceutical company development of large scale purification of human AAT, the FDA approved the use of weekly AAT augmentation therapy for AATD following a clinical trial which demonstrated that weekly infusions would raise to normal plasma and lung epithelial fluid levels of AAT in AAT-deficient individuals. The therapy is now used worldwide to treat AATD, the only pulmonary genetic disease with effective therapy for all affected individuals.

publication date

  • March 2013

has subject area

  • Evidence-Based Medicine
  • Humans
  • Registries
  • Serine Proteinase Inhibitors
  • alpha 1-Antitrypsin
  • alpha 1-Antitrypsin Deficiency

Research

keywords

  • Journal Article
  • Review

Identity

Language

  • eng

Digital Object Identifier (DOI)

  • 10.3109/15412555.2013.764402

PubMed ID

  • 23527997

Additional Document Info

start page

  • 64

end page

  • 67

volume

  • 10 Suppl 1