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

被引:9
|
作者
Baranovski, Boris M. [1 ]
Schuster, Ronen [1 ]
Nisim, Omer [1 ]
Brami, Ido [1 ]
Lior, Yotam [1 ]
Lewis, Eli C. [1 ]
机构
[1] Ben Gurion Univ Negev, Fac Hlth Sci, Dept Clin Biochem & Pharmacol, POB 151, IL-8410501 Beer Sheva, Israel
关键词
autoimmunity; bone-marrow transplantation; cell survival; diabetes; immune system; inflammation; leukemia; organ transplantation; ulcerative colitis; wound healing; OBSTRUCTIVE PULMONARY-DISEASE; ALPHA(1)-ANTITRYPSIN DEFICIENCY; AUGMENTATION THERAPY; LUNG TRANSPLANTATION; CIRCULATING ALPHA-1-ANTITRYPSIN; INFLAMMATORY RESPONSE; INTERNATIONAL SOCIETY; AIRWAY INFLAMMATION; MZ HETEROZYGOTES; CYSTIC-FIBROSIS;
D O I
10.15326/jcopdf.5.4.2017.0161
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
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.
引用
收藏
页码:267 / 276
页数:10
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