Current and Prospective Targets of Pharmacologic Treatment of Hereditary Angioedema Types 1 and 2

被引:31
|
作者
Fijen, Laure M. [1 ]
Bork, Konrad [2 ]
Cohn, Danny M. [1 ]
机构
[1] Univ Amsterdam, Amsterdam UMC, Dept Vasc Med, Amsterdam, Netherlands
[2] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Dept Dermatol, Mainz, Germany
关键词
Hereditary angioedema; C1-inhibitor; Bradykinin; Contact activation system; Kallikrein/kinin system; Serine protease; ORAL KALLIKREIN INHIBITOR; ACUTE ATTACKS; CONTACT ACTIVATION; C1; INHIBITOR; ECALLANTIDE TREATMENT; FACTOR-XII; C1-INHIBITOR; PLASMA; PROPHYLAXIS; TERM;
D O I
10.1007/s12016-021-08832-x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:66 / 76
页数:11
相关论文
共 50 条
  • [31] TREATMENT OF ACUTE ATTACKS OF HEREDITARY ANGIOEDEMA WITH C1-INHIBITOR CONCENTRATE
    AGOSTONI, A
    BERGAMASCHINI, L
    MARTIGNONI, G
    CICARDI, M
    MARASINI, B
    ANNALS OF ALLERGY, 1980, 44 (05): : 299 - 301
  • [32] Current options for prophylactic treatment of hereditary angioedema in the United States: patient-based considerations
    Gower, Richard G.
    Lumry, William R.
    Davis-Lorton, Mark A.
    Johnston, Douglas T.
    Busse, Paula J.
    ALLERGY AND ASTHMA PROCEEDINGS, 2012, 33 (03) : 235 - 240
  • [33] Current characteristics associated with hereditary angioedema attacks and treatment: The home infusion based patient experience
    Tachdjian, Raffi
    Banerji, Aleena
    Guyer, Autumn
    Morphew, Tricia
    ALLERGY AND ASTHMA PROCEEDINGS, 2015, 36 (02) : 151 - 159
  • [34] Abdominal attacks and treatment in hereditary angioedema with C1-inhibitor deficiency
    Eitan Rubinstein
    Leslie E Stolz
    Albert L Sheffer
    Chris Stevens
    Athos Bousvaros
    BMC Gastroenterology, 14
  • [35] Nanofiltrated C1-esterase-inhibitor in the prophylactic treatment of hereditary angioedema
    Strassen, U.
    Bas, M.
    Hajdu, Z.
    Buchberger, M.
    ALLERGY, 2013, 68 : 251 - 251
  • [36] A focus on the use of subcutaneous C1-inhibitor for treatment of hereditary angioedema
    Villavicencio, Maria Fernanda
    Craig, Timothy
    EXPERT REVIEW OF CLINICAL IMMUNOLOGY, 2020, 16 (05) : 451 - 455
  • [37] TREATMENT OF HEREDITARY ANGIOEDEMA DUE TO C1 INHIBITOR DEFICIENCY IN ARGENTINA
    Malbran, Eloisa
    Menendez, Alejandra
    Malbran, Alejandro
    MEDICINA-BUENOS AIRES, 2017, 77 (04) : 279 - 282
  • [38] Abdominal attacks and treatment in hereditary angioedema with C1-inhibitor deficiency
    Rubinstein, Eitan
    Stolz, Leslie E.
    Sheffer, Albert L.
    Stevens, Chris
    Bousvaros, Athos
    BMC GASTROENTEROLOGY, 2014, 14
  • [39] Hereditary Angioedema with Normal C1 Inhibitor Update on Evaluation and Treatment
    Magerl, Markus
    Germenis, Anastasios E.
    Maas, Coen
    Maurer, Marcus
    IMMUNOLOGY AND ALLERGY CLINICS OF NORTH AMERICA, 2017, 37 (03) : 571 - +
  • [40] Diagnosis and treatment of hereditary angioedema with normal C1-inhibitor level
    Emelyanov, A., V
    Leshenkova, E., V
    Kameneva, G. A.
    TERAPEVTICHESKII ARKHIV, 2020, 92 (12) : 86 - 90