1. Current and Prospective Targets of Pharmacologic Treatment of Hereditary Angioedema Types 1 and 2
- Author
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Fijen, Lauré M., Bork, Konrad, and Cohn, Danny M.
- Subjects
medicine.medical_specialty ,C1-inhibitor ,Bradykinin ,Article ,Pharmacological treatment ,03 medical and health sciences ,Preclinical research ,0302 clinical medicine ,Quality of life ,Contact activation system ,medicine ,Humans ,Immunology and Allergy ,Prospective Studies ,030212 general & internal medicine ,Intensive care medicine ,Adverse effect ,Hereditary angioedema ,Hereditary Angioedema Types I and II ,biology ,business.industry ,Angioedemas, Hereditary ,General Medicine ,medicine.disease ,Kallikrein/kinin system ,Serine protease ,On demand treatment ,030228 respiratory system ,Quality of Life ,biology.protein ,business ,Complement C1 Inhibitor Protein ,Rare disease - Abstract
Hereditary angioedema (HAE) is a rare disease that causes episodic attacks of subcutaneous and submucosal edema, which can be painful, incapacitating, and potentially fatal. These attacks are mediated by excessive bradykinin production, as a result of uncontrolled activation of the plasma kallikrein/kinin system, which is caused by a C1 esterase inhibitor deficiency or dysfunction in HAE types 1 and 2, respectively. For many years, treatment options were limited to therapies with substantial adverse effects, insufficient efficacy, or difficult routes of administration. Increased insights in the pathophysiology of HAE have paved the way for the development of new therapies with fewer side effects. In the last two decades, several targeted novel therapeutic strategies for HAE have been developed, for both long-term prophylaxis and on demand treatment of acute attacks. This article reviews the advances in the development of more effective and convenient treatment options for HAE and their anticipated effects on morbidity, mortality, and quality of life. The emergence of these improved treatment options will presumably change current HAE guidelines, but adherence to these recommendations may become restricted by high treatment costs. It will therefore be essential to determine the indications and identify the patients that will benefit most from these newest treatment generations. Ultimately, current preclinical research into gene therapies may eventually lead the way towards curative treatment options for HAE. In conclusion, an increasing shift towards the use of highly effective long-term prophylaxis is anticipated, which should drastically abate the burden on patients with hereditary angioedema.
- Published
- 2021