Mechanisms of allergen specific immunotherapy - T-cell tolerance and more

被引:115
作者
Jutel, M.
Akdis, M.
Blaser, K.
Akdis, C. A.
机构
[1] Swiss Inst Allergy & Asthma Res, CH-7270 Davos, Switzerland
[2] Wroclaw Med Univ, Dept Internal Med & Allergol, Wroclaw, Poland
关键词
allergy; histamine; immunoglobulins; specific immunotherapy; T-regulatory cells; tolerance;
D O I
10.1111/j.1398-9995.2006.01175.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Specific immune suppression and induction of tolerance are essential processes in the regulation and circumvention of immune defence. The balance between allergen-specific T-regulatory (Treg) cells and T helper 2 cells appears to be decisive in the development of allergic and healthy immune response against allergens. Treg cells consistently represent the dominant subset specific for common environmental allergens in healthy individuals. In contrast, there is a high frequency of allergen-specific T helper 2 cells in allergic individuals. A decrease in interleukin (IL)-4, IL-5 and IL-13 production by allergen-specific CD4(+) T cells due to the induction of peripheral T cell tolerance is the most essential step in allergen-specific immunotherapy (SIT). Suppressed proliferative and cytokine responses against the major allergens are induced by multiple suppressor factors, such as cytokines like IL-10 and transforming growth factor (TGF)-beta and cell surface molecules like cytotoxic T lymphocyte antigen-4, programmed death-1 and histamine receptor 2. There is considerable rationale for targeting T cells to increase efficacy of SIT. Such novel approaches include the use of modified allergens produced using recombinant DNA technology and adjuvants or additional drugs, which may increase the generation of allergen-specific peripheral tolerance. By the application of the recent knowledge in Treg cells and related mechanisms of peripheral tolerance, more rational and safer approaches are awaiting for the future of prevention and cure of allergic diseases.
引用
收藏
页码:796 / 807
页数:12
相关论文
共 136 条
[1]   Apoptosis in tissue inflammation and allergic disease [J].
Akdis, CA ;
Blaser, K ;
Akdis, M .
CURRENT OPINION IN IMMUNOLOGY, 2004, 16 (06) :717-723
[2]   Role of interleukin 10 in specific immunotherapy [J].
Akdis, CA ;
Blesken, T ;
Akdis, M ;
Wüthrich, B ;
Blaser, K .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (01) :98-106
[3]   Immune regulation in atonic dermatitis [J].
Akdis, CA ;
Akdis, M ;
Trautmann, A ;
Blaser, K .
CURRENT OPINION IN IMMUNOLOGY, 2000, 12 (06) :641-646
[4]   Genes of tolerance [J].
Akdis, CA ;
Blaser, K ;
Akdis, M .
ALLERGY, 2004, 59 (09) :897-913
[5]   Histamine in the immune regulation of allergic inflammation [J].
Akdis, CA ;
Blaser, K .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2003, 112 (01) :15-22
[6]   IL-10-induced anergy in peripheral T cell and reactivation by microenvironmental cytokines: two key steps in specific immunotherapy [J].
Akdis, CA ;
Blaser, K .
FASEB JOURNAL, 1999, 13 (06) :603-609
[7]   Epitope-specific T cell tolerance to phospholipase A(2) in bee venom immunotherapy and recovery by IL-2 and IL-15 in vitro [J].
Akdis, CA ;
Akdis, M ;
Blesken, T ;
Wymann, D ;
Alkan, SS ;
Muller, U ;
Blaser, K .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (07) :1676-1683
[8]   T helper (Th) 2 predominance in atopic diseases is due to preferential apoptosis of circulating memory/effector Th1 cells [J].
Akdis, M ;
Trautmann, A ;
Klunker, S ;
Daigle, I ;
Küçüksezer, UC ;
Deglmann, W ;
Disch, R ;
Blaser, K ;
Akdis, CA .
FASEB JOURNAL, 2003, 17 (09) :1026-1035
[9]  
Akdis M, 1999, J IMMUNOL, V163, P466
[10]   Immune responses in healthy and allergic individuals are characterized by a fine balance between allergen-specific T regulatory 1 and T helper 2 cells [J].
Akdis, M ;
Verhagen, J ;
Taylor, A ;
Karamloo, F ;
Karagiannidis, C ;
Crameri, R ;
Thunberg, S ;
Deniz, G ;
Valenta, R ;
Fiebig, H ;
Kegel, C ;
Disch, R ;
Schmidt-Weber, CB ;
Blaser, K ;
Akdis, CA .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 199 (11) :1567-1575