The Story of Angioedema: from Quincke to Bradykinin

被引:43
作者
Reshef, Avner [1 ]
Kidon, Mona [2 ,3 ]
Leibovich, Iris [1 ]
机构
[1] Sheba Med Ctr, Angioedema Ctr, Allergy & Clin Immunol, IL-52621 Ramat Gan, Israel
[2] Sheba Med Ctr, Safra Pediat Hosp, Tel Hashomer, Israel
[3] Tel Aviv Univ, Sackler Sch Med, Tel Aviv, Israel
关键词
Swelling; History; Angioedema; Complement; Bradykinin; Fibrinolysis; Prodromes; Clinical guidelines; HEREDITARY ANGIONEUROTIC-EDEMA; C1 INHIBITOR DEFICIENCY; COAGULATION-FACTOR-XII; MOLECULAR-WEIGHT KININOGEN; INTERNATIONAL CONSENSUS ALGORITHM; GLOBULIN PERMEABILITY FACTOR; HUMAN C1BAR INHIBITOR; HUMAN HAGEMAN-FACTOR; ACUTE ATTACKS; DOUBLE-BLIND;
D O I
10.1007/s12016-016-8553-8
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
The term "swelling" has been used in the old scriptures to illustrate a change of normal figure and, as such, an expression of illness. It should be noted that in ancient times, human diseases were very often regarded a punishment from God. Hence, it is not surprising that one of the oldest tests for infidelity involved swelling as an inflicted punishment. The great Greek physician Hippocrates (377-460 BC), considered one of the most outstanding figures in the history of medicine and "Father of the Western Medicine," already used the term oidA"ma to describe swelling of organs. It took many centuries later until the first description of angioedema as a distinct medical entity was minted by Quinke in 1882. The historical progression in angioedema research has been characterized by intermittent "leaps" in interest and scientific achievements. As an example, it took 75 years from the accurate description of hereditary angioedema (HAE) by Osler (1888), until a group of researchers headed by Donaldson (1963) disclosed the central role of C1 inhibitor in angioedema pathophysiology. What followed was a result of a collective effort by many researchers and scientific groups who were able to elucidate the intricate connections between the implicated biochemical pathways. Still, scientific progress was hardly translated into effective therapy, and another 45 years had to elapse until the renewed interest in HAE was boosted by studies on the efficacy and safety of novel therapies about 10 years ago. In the twenty-first century, HAE ceased to be an "orphan disease" and its future is far more optimistic. It is better managed now by specialized angioedema centers, harmonized clinical guidelines, educational programs, laboratory services, and continued basic and clinical research. Patient associations worldwide are offering support and guidance, and governments and healthcare systems are gradually addressing patient and family needs.
引用
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页码:121 / 139
页数:19
相关论文
共 188 条
[1]  
Abelous JE, 1909, CR SOC BIOL, V66, P511
[2]   DANAZOL AND STANOZOLOL IN LONG-TERM PROPHYLACTIC TREATMENT OF HEREDITARY ANGIOEDEMA [J].
AGOSTONI, A ;
CICARDI, M ;
MARTIGNONI, GC ;
BERGAMASCHINI, L ;
MARASINI, B .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1980, 65 (01) :75-79
[3]   Hereditary and acquired angioedema: Problems and progress: Proceedings of the third C1 esterase inhibitor deficiency workshop and beyond [J].
Agostoni, Angelo ;
Aygoeren-Puersuen, Emel ;
Binkley, Karen E. ;
Blanch, Alvaro ;
Bork, Konrad ;
Bouillet, Laurence ;
Bucher, Christoph ;
Castaldo, Anthony J. ;
Cicardi, Marco ;
Davis, Alvin E., III ;
De Carolis, Caterina ;
Drouet, Christian ;
Duponchel, Christiane ;
Farkas, Henriette ;
Fay, Kalman ;
Fekete, Bela ;
Fischer, Bettina ;
Fontana, Luigi ;
Fuest, George ;
Giacomelli, Roberto ;
Groener, Albrecht ;
Hack, C. Erik ;
Harmat, George ;
Jakenfelds, John ;
Juers, Mathias ;
Kalmar, Lajos ;
Kaposi, Pal N. ;
Karadi, Istvan ;
Kitzinger, Arianna ;
Kollar, Timea ;
Kreuz, Wolfhart ;
Lakatos, Peter ;
Longhurst, Hilary J. ;
Lopez-Trascasa, Margarita ;
Martinez-Saguer, Inmaculada ;
Monnier, Nicole ;
Nagy, Istvan ;
Nemeth, Eva ;
Nielsen, Erik Waage ;
Nuijens, Jan H. ;
O'Grady, Caroline ;
Pappalardo, Emanuela ;
Penna, Vincenzo ;
Perricone, Carlo ;
Perricone, Roberto ;
Rauch, Ursula ;
Roche, Olga ;
Rusicke, Eva ;
Spaeth, Peter J. ;
Szendei, George .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2004, 114 (03) :S51-S131
[4]   AUTOANTIBODY-MEDIATED ACQUIRED DEFICIENCY OF C1 INHIBITOR [J].
ALSENZ, J ;
BORK, K ;
LOOS, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 316 (22) :1360-1366
[5]  
ATKINSON JP, 1979, ANN ALLERGY, V42, P349
[6]   DETECTION OF HEREDITARY ANGIONEUROTIC EDEMA BY DEMONSTRATION OF A REDUCTION IN SECOND COMPONENT OF HUMAN COMPLEMENT [J].
AUSTEN, KF ;
SHEFFER, AL .
NEW ENGLAND JOURNAL OF MEDICINE, 1965, 272 (13) :649-&
[7]  
Bannister H. M., 1894, J NERV MENT DIS, V21, P627, DOI [10.1097/00005053-189410000-00002, DOI 10.1097/00005053-189410000-00002]
[8]   Successful use of oxandrolone in the prophylaxis of hereditary angioedema: A case report [J].
Barakat, AJ ;
Castaldo, AJ .
PEDIATRIC ASTHMA ALLERGY & IMMUNOLOGY, 1999, 13 (04) :189-193
[9]  
Barnett A F, 1948, Calif Med, V69, P376
[10]   Case report: first successful application of preimplantation genetic diagnosis for hereditary angiooedema [J].
Bautista-Llacer, Rosa ;
Alberola, Trinitat M. ;
Vendrell, Xavier ;
Fernandez, Esther ;
Perez-Alonso, Manuel .
REPRODUCTIVE BIOMEDICINE ONLINE, 2010, 21 (05) :658-662