Secreted Phospholipases A2 in Hereditary Angioedema With C1-Inhibitor Deficiency

Secreted Phospholipases A2 in Hereditary Angioedema With C1-Inhibitor Deficiency

BackgroundHereditary angioedema (HAE) caused by deficiency (type I) or dysfunction (type II) of the C1 inhibitor protein (C1-INH-HAE) is a disabling, potentially fatal condition characterized by recurrent episodes of swelling. We have recently found that patients with C1-INH-HAE have increased plasm...

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Bibliographic Details
Main Authors: Stefania Loffredo, Anne Lise Ferrara, Maria Bova, Francesco Borriello, Chiara Suffritti, Nóra Veszeli, Angelica Petraroli, Maria Rosaria Galdiero, Gilda Varricchi, Francescopaolo Granata, Andrea Zanichelli, Henriette Farkas, Marco Cicardi, Gérard Lambeau, Gianni Marone
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-07-01
Series:Frontiers in Immunology
Subjects:
hereditary angioedema
angiogenesis
angiopoietins
C1 inhibitor deficiency
vascular endothelial growth factor
vascular permeability
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2018.01721/full

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https://www.frontiersin.org/article/10.3389/fimmu.2018.01721/full

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