Mucosal tolerance to KLH reduces BSA-induced arthritis in rats - An indication of bystander suppression

被引:9
作者
Freysdottir, Jona
Hardardottir, Ingibjorg
Gizurarson, Sveinbjorn
Vikingsson, Arnor
机构
[1] Landspitali Univ Hosp, Ctr Rheumatol Res, IS-101 Reykjavik, Iceland
[2] Lyfjathroun Hf Biopharmaceut, Reykjavik, Iceland
[3] Univ Iceland, Dept Biochem & Mol Biol, Fac Med, Reykjavik, Iceland
[4] Univ Iceland, Fac Pharm, Reykjavik, Iceland
[5] Landspitali Univ Hosp, Dept Rheumatol, IS-101 Reykjavik, Iceland
关键词
nasal tolerance; mucosal tolerance; BSA-induced arthritis; bystander suppression; passive cigarette smoke; anti-inflammatory drugs;
D O I
10.1007/s10875-007-9081-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Mucosal tolerance has been shown to reduce disease severity in animal models mimicking human autoimmune diseases. The objective of this study was to examine whether mucosal tolerance against keyhole limpet haemocyanin (KLH) could be used to reduce bovine serum albumin (BSA)-induced arthritis in rats and whether anti-inflammatory drugs or passive cigarette smoke affected tolerance induction. Arthritis was induced by immunizing rats with BSA and then injecting BSA into one knee and saline into the other knee for comparison. Prior to BSA immunization, the rats were treated intranasally with KLH or saline and KLH then injected in the knee joints at the time of BSA injection, or the rats were treated with or without anti-inflammatory drugs or subjected to cigarette smoke prior to and during intranasal treatment with BSA. The rats that received intranasal treatment with KLH had a significantly less inflammation in their left knee joint compared to rats that received intranasal saline treatment. Beclamethasone increased the tolerance effect of BSA, whereas passive cigarette smoke abrogated the mucosal tolerance. This data suggests that bystander suppression can be used to treat arthritis and other autoimmune diseases, even when the autoantigen is not known.
引用
收藏
页码:284 / 293
页数:10
相关论文
共 46 条
[1]
Barnett ML, 1998, ARTHRITIS RHEUM, V41, P290, DOI 10.1002/1529-0131(199802)41:2<290::AID-ART13>3.3.CO
[2]
2-I
[3]
Abrogation of oral tolerance by feeding encapsulated antigen [J].
Barone, KS ;
Reilly, MR ;
Flanagan, MP ;
Michael, JG .
CELLULAR IMMUNOLOGY, 2000, 199 (02) :65-72
[4]
The [173-196] fragment of ovalbumin suppresses ovalbumin-specific rat IgE responses [J].
Ben Nasser, I ;
Boyaka, PN ;
Ben Aissa, FF ;
Jeddi, M ;
Tome, D .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2003, 3 (12) :1569-1579
[5]
BRAUER R, 1994, EXP TOXICOL PATHOL, V46, P383
[6]
Oral insulin administration and residual β-cell function in recent-onset type 1 diabetes:: a multicentre randomised controlled trial [J].
Chaillous, L ;
Lefèvre, H ;
Thivolet, C ;
Boitard, C ;
Lahlou, N ;
Atlan-Gepner, C ;
Bouhanick, B ;
Mogenet, A ;
Nicolino, M ;
Carel, JC ;
Lecomte, P ;
Maréchaud, R ;
Bougnères, P ;
Charbonnel, B ;
Saï, P .
LANCET, 2000, 356 (9229) :545-549
[7]
REGULATORY T-CELL CLONES INDUCED BY ORAL TOLERANCE - SUPPRESSION OF AUTOIMMUNE ENCEPHALOMYELITIS [J].
CHEN, YH ;
KUCHROO, VK ;
INOBE, J ;
HAFLER, DA ;
WEINER, HL .
SCIENCE, 1994, 265 (5176) :1237-1240
[8]
Choy EHS, 2001, ARTHRITIS RHEUM-US, V44, P1993, DOI 10.1002/1529-0131(200109)44:9<1993::AID-ART347>3.0.CO
[9]
2-A
[10]
The β2-adrenergic agonist salbutamol potentiates oral induction of tolerance, suppressing adjuvant arthritis and antigen-specific immunity [J].
Cobelens, PM ;
Kavelaars, A ;
Vroon, A ;
Ringeling, M ;
van der Zee, R ;
van Eden, W ;
Heijnen, CJ .
JOURNAL OF IMMUNOLOGY, 2002, 169 (09) :5028-5035