Neutrophil activation during attacks in patients with hereditary angioedema due to C1-inhibitor deficiency

被引：0
作者：
Nóra Veszeli
Dorottya Csuka
Zsuzsanna Zotter
Éva Imreh
Mihály Józsi
Szabolcs Benedek
Lilian Varga
Henriette Farkas
机构：
[1] Semmelweis University,Hungarian Angioedema Center, 3rd Department of Internal Medicine
[2] Medical Center,Urology Department
[3] Hungarian Defence Forces,Central Laboratory
[4] Kútvölgyi Clinical Block,MTA
[5] Eötvös Loránd University,ELTE “Lendület” Complement Research Group, Department of Immunology
[6] Semmelweis University,Haematology Unit, 3rd Department of Internal Medicine
来源：
Orphanet Journal of Rare Diseases | / 10卷
关键词：
Hereditary angioedema; C1-inhibitor deficiency; Edematous attack; Neutrophil granulocytes; Neutrophil activation; Neutrophil elastase; Myeloperoxidase; IL-8; TNF-α;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
相关论文
共 50 条
  • [31] Advances in Hereditary Angioedema: The Prevention of Angioedema Attacks With Subcutaneous C1-Inhibitor Replacement Therapy
    Lumry, William
    Templeton, Teri
    Omert, Laurel
    Levy, Donald
    JOURNAL OF INFUSION NURSING, 2020, 43 (03) : 134 - 145
  • [32] Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE)
    Parsopoulou, Faidra
    Loules, Gedeon
    Zamanakou, Maria
    Csuka, Dorottya
    Szilagyi, Agnes
    Kompoti, Maria
    Porebski, Grzegorz
    Psarros, Fotis
    Magerl, Markus
    Valerieva, Anna
    Staevska, Maria
    Obtulowicz, Krystyna
    Maurer, Marcus
    Speletas, Matthaios
    Farkas, Henriette
    Germenis, Anastasios E.
    FRONTIERS IN ALLERGY, 2022, 3
  • [33] Comorbidities in Angioedema Due to C1-Inhibitor Deficiency: An Italian Survey
    Zanichelli, Andrea
    Senter, Riccardo
    Merlo, Andrea
    Gidaro, Antonio
    Janu, Valentina Popescu
    Cogliati, Chiara Beatrice
    Cancian, Mauro
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE, 2024, 12 (04) : 1029 - 1036
  • [34] rhC1INH: a new drug for the treatment of attacks in hereditary angioedema caused by C1-inhibitor deficiency
    Lilian Varga
    Henriette Farkas
    EXPERT REVIEW OF CLINICAL IMMUNOLOGY, 2011, 7 (02) : 143 - 153
  • [35] Glucocorticoid receptor gene polymorphisms in hereditary angioedema with C1-inhibitor deficiency
    Zotter, Zsuzsanna
    Nagy, Zsolt
    Patocs, Attila
    Csuka, Dorottya
    Veszeli, Nora
    Kohalmi, Kinga Viktoria
    Farkas, Henriette
    ORPHANET JOURNAL OF RARE DISEASES, 2017, 12
  • [36] Glucocorticoid receptor gene polymorphisms in hereditary angioedema with C1-inhibitor deficiency
    Zsuzsanna Zotter
    Zsolt Nagy
    Attila Patócs
    Dorottya Csuka
    Nóra Veszeli
    Kinga Viktória Kőhalmi
    Henriette Farkas
    Orphanet Journal of Rare Diseases, 12
  • [37] Secreted Phospholipases A2 in Hereditary Angioedema With C1-Inhibitor Deficiency
    Loffredo, Stefania
    Ferrara, Anne Lise
    Bova, Maria
    Borriello, Francesco
    Suffritti, Chiara
    Veszeli, Nora
    Petraroli, Angelica
    Galdiero, Maria Rosaria
    Varricchi, Gilda
    Granata, Francescopaolo
    Zanichelli, Andrea
    Farkas, Henriette
    Cicardi, Marco
    Lambeau, Gerard
    Marone, Gianni
    FRONTIERS IN IMMUNOLOGY, 2018, 9
  • [38] Cinryze™ (C1-inhibitor) for the treatment of hereditary angioedema
    Gompels, Mark M.
    Lock, Robert John
    EXPERT REVIEW OF CLINICAL IMMUNOLOGY, 2011, 7 (05) : 569 - 573
  • [39] C1 Inhibitor Activity and Angioedema Attacks in Patients with Hereditary Angioedema
    Kaplan, Allen P.
    Pawaskar, Dipti
    Chiao, Joseph
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE, 2020, 8 (03) : 892 - 900
  • [40] A follow-up survey of patients with acquired angioedema due to C1-inhibitor deficiency
    Polai, Zs.
    Balla, Zs.
    Andrasi, N.
    Kohalmi, K. V.
    Temesszentandrasi, Gy.
    Benedek, Sz.
    Varga, L.
    Farkas, H.
    JOURNAL OF INTERNAL MEDICINE, 2021, 289 (04) : 547 - 558
12345