Immunotherapy of asthma using CpG oligodeoxynucleotides

被引:18
作者
Kline, Joel N. [1 ]
机构
[1] Univ Iowa, Roy J & Lucille A Carver Coll Med, Grad Program Immunol, Dept Med, Iowa City, IA 52242 USA
关键词
asthma; hygiene hypothesis; immunotherapy; CpG oligodeoxynucleotides; T-regulatory cells;
D O I
10.1007/s12026-007-0083-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Asthma and other atopic disorders have increased in prevalence and severity over the past three decades. Reduced risk of atopic disease associated with early life exposure to infections and microbes has raised the possibility that pathogen-associated molecular patterns (PAMPs) may confer protection against allergic disorders, a concept that has been named the "Hygiene Hypothesis". This relationship is most likely mediated through the induction of specific patterns of anti-atopic immune responses that follow engagement of innate immune mechanisms. Bacterial DNA is one such immunostimulatory microbe-associated ligand, whose properties can be mimicked by oligodeoxynucleotides (ODN) containing unmethylated cytosine-guanine dinucleotides in specific base sequences (CpG motifs), motifs characteristic of prokaryotic DNA that have been suppressed in eukaryotic DNA. Based initially on observations that CpG ODN induced Th1-type patterns of immune responses, we proposed that CpG ODN might represent a novel therapeutic strategy for the prevention and treatment of atopic disorders. Current understanding suggests multiple mechanisms of action of CpG ODN, but our initial hypothesis has been supported by extensive studies demonstrating, in animal models, efficacy in both incipient and established atopic asthma. These preclinical studies are now being translated into clinical trials exploring this new approach to immunotherapy for atopic disease.
引用
收藏
页码:279 / 286
页数:8
相关论文
共 23 条
[1]   Environmental exposure to endotoxin and its relation to asthma in school-age children [J].
Braun-Fahrländer, C ;
Riedler, J ;
Herz, U ;
Eder, W ;
Waser, M ;
Grize, L ;
Maisch, S ;
Carr, D ;
Gerlach, F ;
Bufe, A ;
Lauener, RP ;
Schierl, R ;
Renz, H ;
Nowak, D ;
von Mutius, E .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (12) :869-877
[2]   Bacterial DNA-induced NK cell IFN-gamma production is dependent on macrophage secretion of IL-12 [J].
Chace, JH ;
Hooker, NA ;
Mildenstein, KL ;
Krieg, AM ;
Cowdery, JS .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1997, 84 (02) :185-193
[3]   CpG oligodeoxynucleotides act as adjuvants that switch on T helper 1 (Th1) immunity [J].
Chu, RS ;
Targoni, OS ;
Krieg, AM ;
Lehmann, PV ;
Harding, CV .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (10) :1623-1631
[4]  
Cowdery J, 1996, J IMMUNOL, V156, P4570
[5]   Mucosal immunotherapy with CpG oligodeoxynucleotides reverses a murine model of chronic asthma induced by repeated antigen exposure [J].
Jain, VV ;
Businga, TR ;
Kitagaki, K ;
George, CL ;
O'Shaughnessy, PT ;
Kline, JN .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2003, 285 (05) :L1137-L1146
[6]   CpG-oligodeoxynucleotides inhibit airway remodeling in a murine model of chronic asthma [J].
Jain, VV ;
Kitagaki, K ;
Businga, T ;
Hussain, I ;
George, C ;
O'Shaughnessy, P ;
Kline, JN .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2002, 110 (06) :867-872
[7]   Oral administration of CpG-ODNs suppresses antigen-induced asthma in mice [J].
Kitagaki, K ;
Businga, TR ;
Kline, JN .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2006, 143 (02) :249-259
[8]   Immunomodulatory effects of CpG oligodeoxynucleotides on established Th2 responses [J].
Kitagaki, K ;
Jain, VV ;
Businga, TR ;
Hussain, I ;
Kline, JN .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2002, 9 (06) :1260-1269
[9]   CpG oligodeoxynucleotides do not require TH1 cytokines to prevent eosinophilic airway inflammation in a murine model of asthma [J].
Kline, JN ;
Krieg, AM ;
Waldschmidt, TJ ;
Ballas, ZK ;
Jain, V ;
Businga, TR .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1999, 104 (06) :1258-1264
[10]  
Kline JN, 1998, J IMMUNOL, V160, P2555