Immunologic mechanisms of cutaneous drug reactions

被引:27
作者
Merk, HF
Hertl, M
机构
[1] Department of Dermatology, Medical Faculty, University Hospital, 52074 Aachen
关键词
D O I
10.1016/S1085-5629(96)80035-6
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Idiosyncratic reactions (type B) are a major complication of drug therapy, because they are related to both the drug and to individual factors in the host. In comparison with other organs, the skin is quite frequently a target of allergic reactions, which are mainly elicited by small molecular weight compounds. This is the case in allergic contact dermatitis as well as in drug allergic reactions. In contrast to allergic contact dermatitis however, drug-induced hypersensitivity reactions of the skin have an enormous variability with regard to their pathophysiological pathways, clinical signs of symptoms, severity, and the drugs which can elicit these reactions. Allergic reactions are mediated either by specific antibodies or a cellular immunocompetent immune response. About 25% to 30% of type B reactions are estimated to be allergic drug reactions, which are classified by the latency period between the ingestion of the responsible allergen and the onset of clinical symptoms. Studying the mechanisms of these hypersensitivity reactions improves our understanding of these diseases in general, and shows the importance of the skin as a signaling organ in these reactions. Copyright (C) 1996 by W.B. Saunders Company.
引用
收藏
页码:228 / 235
页数:8
相关论文
共 54 条
[41]   SEVERE ADVERSE CUTANEOUS REACTIONS TO DRUGS [J].
ROUJEAU, JC ;
STERN, RS .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (19) :1272-1285
[42]   MEDICATION USE AND THE RISK OF STEVENS-JOHNSON SYNDROME OR TOXIC EPIDERMAL NECROLYSIS [J].
ROUJEAU, JC ;
KELLY, JP ;
NALDI, L ;
RZANY, B ;
STERN, RS ;
ANDERSON, T ;
AUQUIER, A ;
BASTUJIGARIN, S ;
CORREIA, O ;
LOCATI, F ;
MOCKENHAUPT, M ;
PAOLETTI, C ;
SHAPIRO, S ;
SHEAR, N ;
SCHOPF, E ;
KAUFMAN, DW .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (24) :1600-1607
[43]   BIOCHEMICAL ACANTHOLYSIS PROVOKED BY THIOL DRUGS [J].
RUOCCO, V ;
PISANI, M ;
DEANGELIS, E ;
LOMBARDI, ML .
ARCHIVES OF DERMATOLOGY, 1990, 126 (07) :965-966
[44]  
SCHOPF E, 1995, FORTSCHRITTE DERMATO, P89
[45]  
SCHWARTZ LB, 1989, PROGRESS IN ALLERGY AND CLINICAL IMMUNOLOGY, P1
[46]   TRYPTASE LEVELS AS AN INDICATOR OF MAST-CELL ACTIVATION IN SYSTEMIC-ANAPHYLAXIS AND MASTOCYTOSIS [J].
SCHWARTZ, LB ;
METCALFE, DD ;
MILLER, JS ;
EARL, H ;
SULLIVAN, T .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 316 (26) :1622-1626
[47]   FIXED DRUG ERUPTION - EXPRESSION OF EPIDERMAL KERATINOCYTE INTERCELLULAR-ADHESION MOLECULE-1 (ICAM-1) [J].
SHIOHARA, T ;
NICKOLOFF, BJ ;
SAGAWA, Y ;
GOMI, T ;
NAGASHIMA, M .
ARCHIVES OF DERMATOLOGY, 1989, 125 (10) :1371-1376
[48]  
SULLIVAN TJ, 1994, CLIN MANAGEMENT URTI, P119
[49]   ASSOCIATION OF ANTIBODY TO HISTONE COMPLEX H2A-H2B WITH SYMPTOMATIC PROCAINAMIDE-INDUCED LUPUS [J].
TOTORITIS, MC ;
TAN, EM ;
MCNALLY, EM ;
RUBIN, RL .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 318 (22) :1431-1436
[50]  
TSUTSUI H, 1992, J IMMUNOL, V149, P706