The seronegative spondyloarthropathies are a group of inflammatory diseases in which the spine, peripheral joints, skin, eyes, and other tissues of the body may be involved. There are many common clinical, radiological and pathological features. The observation of the strong association of HLA-B27 antigen (60-90% compared to 8% in the normal population) has further strengthened the commonality among these diseases. The development of Reiter's syndrome and reactive arthritis in B27 positive individuals occurs after gastrointestinal infection with one of several species of bacteria, including Yersinia, Salmonella, Shigella, Campylobacter, and Chlamydia. In addition, the work from several laboratories suggest that Klebsiella pneumoniae may play a role in the pathogenesis of ankylosing spondylitis in B27 positive individuals. The mechanisms by which intestinal microbes react with B27 to induce arthritic disease is not known, however, several theories have been postulated. For instance, there may be crossreactivity between HLA-B27 gene have already been developed in our laboratory for this purpose. With these mice, we would like to 1) induce arthritic disease by immunization with intestinal bacteria; and 2) determine which aspect of the interaction between HLA-B27 and bacterial infection is responsible for inducing reactive arthritis. In addition, background and major histocompatibility genes in mice can be easily manipulated so that we can determine whether another gene in linkage disequilibrium with HLA-B27 is necessary for the production of arthritic disease. Determination of the components responsible for the promotion of disease will open several doors to immune intervention and immunotherapy.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
1R01AR039875-01
Application #
3160113
Study Section
General Medicine A Subcommittee 2 (GMA)
Project Start
1989-03-01
Project End
1992-02-29
Budget Start
1989-03-01
Budget End
1990-02-28
Support Year
1
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Mayo Clinic, Rochester
Department
Type
DUNS #
City
Rochester
State
MN
Country
United States
Zip Code
55905
Khare, S D; Lee, S; Bull, M J et al. (2001) Spontaneous inflammatory disease in HLA-B27 transgenic mice does not require transporter of antigenic peptides. Clin Immunol 98:364-9
Lee, S; Khare, S D; Griffiths, M M et al. (2000) HLA-B27 transgenic mice are susceptible to collagen-induced arthritis: type II collagen as a potential target in human disease. Hum Immunol 61:140-7
Khare, S D; Lee, S; Bull, M J et al. (1999) Peptide binding alpha1alpha2 domain of HLA-B27 contributes to the disease pathogenesis in transgenic mice. Hum Immunol 60:116-26
Khare, S D; Luthra, H S; David, C S (1998) Animal models of human leukocyte antigen B27-linked arthritides. Rheum Dis Clin North Am 24:883-94, xi-xii
Khare, S D; Luthra, H S; David, C S (1998) Unraveling the mystery of HLA-B27 association with human spondyloarthropathies using transgenic and knock out mice. Semin Immunol 10:15-23
Khare, S D; Bull, M J; Hanson, J et al. (1998) Spontaneous inflammatory disease in HLA-B27 transgenic mice is independent of MHC class II molecules: a direct role for B27 heavy chains and not B27-derived peptides. J Immunol 160:101-6
Khare, S D; Luthra, H S; David, C S (1996) Role of HLA-B27 in spondyloarthropathies. Curr Top Microbiol Immunol 206:85-100
Khare, S D; Hansen, J; Luthra, H S et al. (1996) HLA-B27 heavy chains contribute to spontaneous inflammatory disease in B27/human beta2-microglobulin (beta2m) double transgenic mice with disrupted mouse beta2m. J Clin Invest 98:2746-55
Khare, S D; Luthra, H S; David, C S (1995) Spontaneous inflammatory arthritis in HLA-B27 transgenic mice lacking beta 2-microglobulin: a model of human spondyloarthropathies. J Exp Med 182:1153-8
Pedrinaci, S; Hanson, J; David, C (1994) Hierarchy in the assembly of HLA-B27 and HLA-Cw3 molecules in transgenic mice. Immunogenetics 39:130-7

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