Avian models with spontaneous autoimmune diseases

被引:37
作者
Wick, Georg [1 ]
Andersson, Leif
Hala, Karel
Gershwin, M. Eric
Selmi, Carlo
Erf, Gisela F.
Lamont, Susan J.
Sgonc, Roswitha
机构
[1] Innsbruck Med Univ, Div Expt Pathophysiol & Immunol, Bioctr, A-6020 Innsbruck, Austria
[2] Uppsala Univ, Uppsala Biomed Ctr, Dept Med Biochem & Microbiol, SE-75124 Uppsala, Sweden
[3] Swedish Univ Agr Sci, Dept Anim Breeding & Genet, SE-75124 Uppsala, Sweden
[4] Univ S Bohemia, Fac Agr, Ceske Budejovice, Czech Republic
[5] Univ Calif Davis, Dept Internal Med, Div Rheumatol Allergy & Clin Immunol, Genome & Biomed Sci Facil, Davis, CA USA
[6] Univ Arkansas, Ctr Excellence Poultry Sci, Fayetteville, AR 72701 USA
[7] Iowa State Univ, Dept Anim Sci, Ames, IA USA
来源
ADVANCES IN IMMUNOLOGY, VOL 92 | 2006年 / 92卷
基金
奥地利科学基金会;
关键词
D O I
10.1016/S0065-2776(06)92002-1
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
Autoimmune diseases in human patients only become clinically manifest when the disease process has developed to a stage where functional compensation by the afflicted organ or system is not possible anymore. In order to understand the initial etiologic and pathogenic events that are generally not yet accessible in humans, appropriate animal models are required. In this respect, spontaneously developing models-albeit rare-reflect the situation in humans much more closely than experimentally induced models, including knockout and transgenic mice. The present chapter describes three spontaneous chicken models for human autoimmune diseases, the Obese strain (OS) with a Hashimoto-like autoimmune thyroiditis, the University of California at Davis lines 200 and 206 (UCD-200 and -206) with a scleroderma-like disease, and the amelanotic Smyth line with a vitiligo-like syndrome (SLV). Special emphasis is given to the new opportunities to unravel the genetic basis of these diseases in view of the recently completed sequencing of the chicken genome.
引用
收藏
页码:71 / 117
页数:47
相关论文
共 172 条
[1]
A large database of chicken bursal ESTs as a resource for the analysis of vertebrate gene function [J].
Abdrakhmanov, I ;
Lodygin, D ;
Geroth, P ;
Arakawa, H ;
Law, A ;
Plachy, J ;
Korn, B ;
Buerstedde, JM .
GENOME RESEARCH, 2000, 10 (12) :2062-2069
[2]
GENETIC-CONTROL OF AVIAN SCLERODERMA [J].
ABPLANALP, H ;
GERSHWIN, ME ;
JOHNSTON, E ;
REID, J .
IMMUNOGENETICS, 1990, 31 (5-6) :291-295
[3]
Study on the antioxidant status of vitiligo patients of different age groups in Baroda [J].
Agrawal, D ;
Shajil, EM ;
Marfatia, YS ;
Begum, R .
PIGMENT CELL RESEARCH, 2004, 17 (03) :289-294
[4]
NONTHYROID AUTOANTIBODIES IN OBESE STRAIN (OS) CHICKENS [J].
AICHINGER, G ;
KOFLER, H ;
DIAZMERIDA, O ;
WICK, G .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1984, 32 (01) :57-69
[5]
Domestic-animal genomics: deciphering the genetics of complex traits [J].
Andersson, L ;
Georges, M .
NATURE REVIEWS GENETICS, 2004, 5 (03) :202-212
[6]
Altered procollagen mRNA expression during the progression of avian scleroderma [J].
Ausserlechner, MJ ;
Sgonc, R ;
Dietrich, H ;
Wick, G .
MOLECULAR MEDICINE, 1997, 3 (10) :654-662
[7]
AUSTIN LM, 1995, AM J PATHOL, V146, P1529
[8]
RELATION BETWEEN MAJOR HISTOCOMPATIBILITY (B) LOCUS AND AUTOIMMUNE THYROIDITIS IN OBESE CHICKENS [J].
BACON, LD ;
KITE, JH ;
ROSE, NR .
SCIENCE, 1974, 186 (4160) :274-275
[9]
SEROTYPE SPECIFICITY OF B-HAPLOTYPE INFLUENCE ON THE RELATIVE EFFICACY OF MAREKS-DISEASE VACCINES [J].
BACON, LD ;
WITTER, RL .
AVIAN DISEASES, 1994, 38 (01) :65-71
[10]
Immune-neuro-endocrine interactions: Facts and hypotheses [J].
Besedovsky, HO ;
DelRey, A .
ENDOCRINE REVIEWS, 1996, 17 (01) :64-102