Literature DB >> 30723784

Alpha-1 Antitrypsin Substitution for Extrapulmonary Conditions in Alpha-1 Antitrypsin Deficient Patients.

Boris M Baranovski1, Ronen Schuster1, Omer Nisim1, Ido Brami1, Yotam Lior1, Eli C Lewis1.   

Abstract

Alpha-1 antitrypsin deficiency (AATD) is a genetic disorder which most commonly manifests as pulmonary emphysema. Accordingly, alpha-1 antitrypsin (AAT) augmentation therapy aims to reduce the progression of emphysema, as achieved by life-long weekly slow-drip infusions of plasma-derived affinity-purified human AAT. However, not all AATD patients will receive this therapy, due to either lack of medical coverage or low patient compliance. To circumvent these limitations, attempts are being made to develop lung-directed therapies, including inhaled AAT and locally-delivered AAT gene therapy. Lung transplantation is also an ultimate therapy option. Although less common, AATD patients also present with disease manifestations that extend beyond the lung, including vasculitis, diabetes and panniculitis, and appear to experience longer and more frequent hospitalization times and more frequent pneumonia bouts. In the past decade, new mechanism-based clinical indications for AAT therapy have surfaced, depicting a safe, anti-inflammatory, immunomodulatory and tissue-protective agent. Introduced to non-AATD individuals, AAT appears to provide relief from steroid-refractory graft-versus-host disease, from bacterial infections in cystic fibrosis and from autoimmune diabetes; preclinical studies show benefit also in multiple sclerosis, ulcerative colitis, rheumatoid arthritis, acute myocardial infarction and stroke, as well as ischemia-reperfusion injury and aberrant wound healing processes. While the current augmentation therapy is targeted towards treatment of emphysema, it is suggested that AATD patients may benefit from AAT augmentation therapy geared towards extrapulmonary pathologies as well. Thus, development of mechanism-based, context-specific AAT augmentation therapy protocols is encouraged. In the current review, we will discuss extrapulmonary manifestations of AATD and the potential of AAT augmentation therapy for these conditions.

Entities:  

Keywords:  autoimmunity; bone-marrow transplantation; cell survival; diabetes; immune system; inflammation; leukemia; organ transplantation; ulcerative colitis; wound healing

Year:  2018        PMID: 30723784      PMCID: PMC6361480          DOI: 10.15326/jcopdf.5.4.2017.0161

Source DB:  PubMed          Journal:  Chronic Obstr Pulm Dis        ISSN: 2372-952X


  81 in total

1.  American Thoracic Society/European Respiratory Society statement: standards for the diagnosis and management of individuals with alpha-1 antitrypsin deficiency.

Authors: 
Journal:  Am J Respir Crit Care Med       Date:  2003-10-01       Impact factor: 21.405

2.  Association between airway bacterial load and markers of airway inflammation in patients with stable chronic bronchitis.

Authors:  A T Hill; E J Campbell; S L Hill; D L Bayley; R A Stockley
Journal:  Am J Med       Date:  2000-09       Impact factor: 4.965

3.  Change in lung function and morbidity from chronic obstructive pulmonary disease in alpha1-antitrypsin MZ heterozygotes: A longitudinal study of the general population.

Authors:  Morten Dahl; Anne Tybjaerg-Hansen; Peter Lange; Jørgen Vestbo; Børge G Nordestgaard
Journal:  Ann Intern Med       Date:  2002-02-19       Impact factor: 25.391

4.  Alpha1-antitrypsin monotherapy prolongs islet allograft survival in mice.

Authors:  Eli C Lewis; Leland Shapiro; Owen J Bowers; Charles A Dinarello
Journal:  Proc Natl Acad Sci U S A       Date:  2005-08-10       Impact factor: 11.205

5.  alpha1-Antitrypsin inhalation reduces airway inflammation in cystic fibrosis patients.

Authors:  M Griese; P Latzin; M Kappler; K Weckerle; T Heinzlmaier; T Bernhardt; D Hartl
Journal:  Eur Respir J       Date:  2006-10-18       Impact factor: 16.671

6.  Exacerbations in {alpha}1-antitrypsin deficiency.

Authors:  M Needham; R A Stockley
Journal:  Eur Respir J       Date:  2005-06       Impact factor: 16.671

7.  Augmentation therapy reduces frequency of lung infections in antitrypsin deficiency: a new hypothesis with supporting data.

Authors:  J Lieberman
Journal:  Chest       Date:  2000-11       Impact factor: 9.410

8.  [Panniculitis revealing alpha-1 antitrypsin deficiency. Report of 3 cases].

Authors:  B Albes; P Bayle-Lebey; J Bazex; L Lamant
Journal:  Ann Med Interne (Paris)       Date:  2001-12

Review 9.  Alpha-1-antitrypsin associated panniculitis: the MS variant.

Authors:  Pedram Geraminejad; James R DeBloom; Hobart W Walling; Richard D Sontheimer; Marta VanBeek
Journal:  J Am Acad Dermatol       Date:  2004-10       Impact factor: 11.527

Review 10.  Chronic obstructive pulmonary disease in alpha1-antitrypsin PI MZ heterozygotes: a meta-analysis.

Authors:  C P Hersh; M Dahl; N P Ly; C S Berkey; B G Nordestgaard; E K Silverman
Journal:  Thorax       Date:  2004-10       Impact factor: 9.139

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  3 in total

1.  Is More Better? Promising Biological Effects of Double-Dose Alpha 1-Antitrypsin Therapy.

Authors:  Irina Petrache
Journal:  Am J Respir Crit Care Med       Date:  2019-08-01       Impact factor: 21.405

Review 2.  Post-Translational Modifications of Circulating Alpha-1-Antitrypsin Protein.

Authors:  Urszula Lechowicz; Stefan Rudzinski; Aleksandra Jezela-Stanek; Sabina Janciauskiene; Joanna Chorostowska-Wynimko
Journal:  Int J Mol Sci       Date:  2020-12-02       Impact factor: 5.923

3.  Application of alpha1-antitrypsin in a rat model of veno-arterial extracorporeal membrane oxygenation.

Authors:  Fabian Edinger; Christoph Schmitt; Christian Koch; J Michael McIntosh; Sabina Janciauskiene; Melanie Markmann; Michael Sander; Winfried Padberg; Veronika Grau
Journal:  Sci Rep       Date:  2021-08-04       Impact factor: 4.379

  3 in total

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