Peptide-based immunotherapy:: a novel strategy for allergic disease

被引:23
作者
Ali, F. Runa [1 ]
Larche, Mark [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Fac Med, Dept Allergy & Clin Immunol, Resp Immunol Grp, London SW7 2AZ, England
关键词
allergy; asthma; cytokines; immunotherapy; peptides; T-cells; tolerance;
D O I
10.1586/14760584.4.6.881
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The T-cell component of the antigen-specific immune response is the target of various novel interventions to modify chronic immunologic disorders, such as allergic diseases. Recent clinical trials have evaluated the safety and efficacy of therapeutic vaccines consisting of short, synthetic, allergen-derived peptides, corresponding to T-cell epitopes from the eliciting antigen. The main advantage of such an approach is the reduction in systemic, immunoglobulin E-mediated adverse events compared with existing whole allergen immunotherapy, often referred to as 'allergy shots'. T-cell peptide epitopes, although capable of inducing immunologic tolerance, are short linear structures that have reduced ability to cross-link mast cell- and basophil-bound immunoglobulin E. The precise mechanism of tolerance induction remains incompletely defined. However, recent data indicate that peptide therapy induces/expands a population of antigen-specific regulatory T-cells. A novel form of treatment combining efficacy with a substantially decreased occurrence of adverse events is likely to have a major impact on the management and prevalence of allergic diseases. Furthermore, the principles of epitope-specific therapy hold promise for the development of therapeutic vaccines for the treatment of autoimmune diseases.
引用
收藏
页码:881 / 889
页数:9
相关论文
共 69 条
[1]   Immunotherapy in asthma: an updated systematic review [J].
Abramson, M ;
Puy, R ;
Weiner, J .
ALLERGY, 1999, 54 (10) :1022-1041
[2]   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
[3]   Fel d 1-derived T cell peptide therapy induces recruitment of CD4+CD25+;: CD4+ interferon-γ+ T helper type 1 cells to sites of allergen-induced late-phase skin reactions in cat-allergic subjects [J].
Alexander, C ;
Ying, S ;
Kay, AB ;
Larché, M .
CLINICAL AND EXPERIMENTAL ALLERGY, 2005, 35 (01) :52-58
[4]   Late asthmatic reactions induced by inhalation of allergen-derived T cell peptides [J].
Ali, FR ;
Oldfield, WLG ;
Higashi, N ;
Larché, M ;
Kay, AB .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2004, 169 (01) :20-26
[5]   In vivo instruction of suppressor commitment in naive T cells [J].
Apostolou, I ;
von Boehmer, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 199 (10) :1401-1408
[6]   Inducing tolerance by intranasal administration of long peptides in naive and primed CBA/J mice [J].
Astori, M ;
von Garnier, C ;
Kettner, A ;
Dufour, N ;
Corradin, G ;
Spertini, F .
JOURNAL OF IMMUNOLOGY, 2000, 165 (06) :3497-3505
[7]   ANTIGEN PRESENTATION BY KERATINOCYTES INDUCES TOLERANCE IN HUMAN T-CELLS [J].
BAL, V ;
MCINDOE, A ;
DENTON, G ;
HUDSON, D ;
LOMBARDI, G ;
LAMB, J ;
LECHLER, R .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1990, 20 (09) :1893-1897
[8]   Modulation of the allergic immune response in BALB/c mice by subcutaneous injection of high doses of the dominant T cell epitope from the major birch pollen allergen Bet v 1 [J].
Bauer, L ;
Bohle, B ;
JahnSchmid, B ;
Wiedermann, U ;
Daser, A ;
Renz, H ;
Kraft, D ;
Ebner, C .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 1997, 107 (03) :536-541
[9]   Bystander suppression of murine collagen-induced arthritis by long-term nasal administration of a self type II collagen peptide [J].
Bayrak, S ;
Mitchison, NA .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 1998, 113 (01) :92-95
[10]   Treatment of NOD diabetes with a novel peptide of the hsp60 molecule induces th2-type antibodies [J].
Bockova, J ;
Elias, D ;
Cohen, IR .
JOURNAL OF AUTOIMMUNITY, 1997, 10 (04) :323-329