Literature DB >> 24522092

Endothelial cell activation during edematous attacks of hereditary angioedema types I and II.

Erika Kajdácsi1, Péter K Jani1, Dorottya Csuka1, Lilian Ágnes Varga1, Zoltán Prohászka1, Henriette Farkas1, László Cervenak2.   

Abstract

BACKGROUND: Hereditary angioedema (HAE) caused by C1-inhibitor (C1-INH) deficiency (HAE-C1-INH) is a potentially life-threatening rare disease caused by the decreased activity of C1-INH. Lack of C1-INH leads to overproduction of bradykinin, a potent vasoactive peptide. Although angioedema is induced by bradykinin, the function and activation of endothelial cells (ECs), the targets of bradykinin, have not yet been studied during HAE attacks.
OBJECTIVE: We studied whether EC function is altered during HAE attacks in comparison with attack-free intervals.
METHODS: Forty-six consecutive samples obtained during attacks from 18 patients with HAE-C1-INH were compared with inter-attack samples of the same patients. The patients' sera were tested for von Willebrand factor (VWF) antigen, VWF collagen-binding activity, soluble E-selectin, and endothelin-1 levels by using ELISA and BRAHMS Kryptor technologies.
RESULTS: Levels of all 4 EC markers (VWF antigen, VWF collagen-binding activity, soluble E-selectin, and endothelin-1) were significantly increased during HAE attacks. Their increases were even more obvious in the subgroup of patients without any pre-existing risk factors for endothelial dysfunction.
CONCLUSION: In this study we demonstrated that ECs are activated during HAE attacks. Our results might suggest the need for revising the knowledge on the pathogenesis of HAE-C1-INH and for reconsidering the role of ECs as a possible novel therapeutic target in patients with this disease.
Copyright © 2014 American Academy of Allergy, Asthma & Immunology. Published by Mosby, Inc. All rights reserved.

Entities:  

Keywords:  C1-inhibitor deficiency; Hereditary angioedema; activation; attack; clinical study; endothelial cells; endothelin-1; soluble E-selectin; von Willebrand factor

Mesh:

Substances:

Year:  2014        PMID: 24522092     DOI: 10.1016/j.jaci.2013.12.1072

Source DB:  PubMed          Journal:  J Allergy Clin Immunol        ISSN: 0091-6749            Impact factor:   10.793


  13 in total

Review 1.  HAE Pathophysiology and Underlying Mechanisms.

Authors:  Bruce L Zuraw; Sandra C Christiansen
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2.  Novel Vasoregulatory Aspects of Hereditary Angioedema: the Role of Arginine Vasopressin, Adrenomedullin and Endothelin-1.

Authors:  Erika Kajdácsi; Péter K Jani; Dorottya Csuka; Lilian Varga; Zoltán Prohászka; Henriette Farkas; László Cervenak
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3.  Growth factors and IL-17 in hereditary angioedema.

Authors:  M Salemi; V Mandalà; V Muggeo; G Misiano; S Milano; G Colonna-Romano; F Arcoleo; E Cillari
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Review 4.  "Nuts and Bolts" of Laboratory Evaluation of Angioedema.

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7.  Pathways of Neutrophil Granulocyte Activation in Hereditary Angioedema with C1 Inhibitor Deficiency.

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8.  Elevated D-dimers in attacks of hereditary angioedema are not associated with increased thrombotic risk.

Authors:  A Reshef; A Zanichelli; H Longhurst; A Relan; C E Hack
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9.  Secreted Phospholipases A2 in Hereditary Angioedema With C1-Inhibitor Deficiency.

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Review 10.  Biomarkers in Hereditary Angioedema.

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Journal:  Clin Rev Allergy Immunol       Date:  2021-02-09       Impact factor: 8.667

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