Update on the current status of peptide immunotherapy

被引:74
作者
Larche, Mark [1 ]
机构
[1] McMaster Univ, Fac Hlth Sci, Dept Med, Div Clin Immunol & Allergy,HSC, Hamilton, ON L8N 3Z5, Canada
关键词
epitope; immunologic tolerance; T cell; regulatory T cell; peptide; allergen; immunotherapy; IL-10;
D O I
10.1016/j.jaci.2007.02.015
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
The use of synthetic peptide fragments of allergen molecules holds promise for the delivery of effective immunotherapy without IgE-mediated adverse events. Early studies were associated with frequent induction of allergic symptoms after treatment, mostly related to activation of allergen-specific effector T cells with high doses of peptides. More recently, low doses of peptides have been shown to modify clinical and laboratory surrogates without inducing adverse events. Studies are ongoing to define the optimal dose, dose interval, and route of administration. Current results indicate that treatment with peptides modulates the immune response by reducing T(H)2 responses to allergen and increasing IL-10 production and the activity of allergen-specific regulatory T cells. Further studies are required in larger numbers of subjects and with peptides derived from a variety of allergens.
引用
收藏
页码:906 / 909
页数:4
相关论文
共 15 条
[1]   The effect of Fel d 1-derived T-cell peptides on upper and lower airway outcome measurements in cat-allergic subjects [J].
Alexander, C ;
Tarzi, M ;
Larché, M ;
Kay, AB .
ALLERGY, 2005, 60 (10) :1269-1274
[2]   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
[3]   Allergen-specific T-cell tolerance induction with allergen-derived long synthetic peptides: Results of a phase I trial [J].
Fellrath, JM ;
Kettner, A ;
Dufour, N ;
Frigerio, C ;
Schneeberger, D ;
Leimgruber, A ;
Corradin, G ;
Spertini, F .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2003, 111 (04) :854-861
[4]   Immunoglobulin E-independent major histocompatibility complex-restricted T cell peptide epitope-induced late asthmatic reactions [J].
Haselden, BM ;
Kay, AB ;
Larché, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (12) :1885-1894
[5]   Peptide therapy for allergic diseases:: basic mechanisms and new clinical approaches [J].
Larché, M .
PHARMACOLOGY & THERAPEUTICS, 2005, 108 (03) :353-361
[6]   The safety and efficacy of ALLERVAX CAT in cat allergic patients [J].
Maguire, P ;
Nicodemus, C ;
Robinson, D ;
Aaronson, D ;
Umetsu, DT .
CLINICAL IMMUNOLOGY, 1999, 93 (03) :222-231
[7]   Successful immunotherapy with T-cell epitope peptides of bee venom phospholipase A2 induces specific T-cell anergy in patients allergic to bee venom [J].
Müller, U ;
Akdis, CA ;
Fricker, M ;
Akdis, M ;
Blesken, T ;
Bettens, F ;
Blaser, K .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1998, 101 (06) :747-754
[8]   Treatment of cat allergy with T-cell reactive peptides [J].
Norman, PS ;
Ohman, JL ;
Long, AA ;
Creticos, PS ;
Gefter, MA ;
Shaked, Z ;
Wood, RA ;
Eggleston, PA ;
Hafner, KB ;
Rao, P ;
Lichtenstein, LM ;
Jones, NH ;
Nicodemus, CF .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 154 (06) :1623-1628
[9]   Effect of T-cell peptides derived from Fel d 1 on allergic reactions and cytokine production in patients sensitive to cats:: a randomised controlled trial [J].
Oldfield, WLG ;
Larché, M ;
Kay, AB .
LANCET, 2002, 360 (9326) :47-53
[10]   Allergen-derived T cell peptide-induced late asthmatic reactions precede the induction of antigen-specific hyporesponsiveness in atopic allergic asthmatic subjects [J].
Oldfield, WLG ;
Kay, AB ;
Larché, M .
JOURNAL OF IMMUNOLOGY, 2001, 167 (03) :1734-1739