Kawasaki's disease (KD) is the most common acute vasculitis of childhood and can lead to significant morbidity secondary to the development of coronary arteritis and aneurysms. The present proposal seeks to determine the potential role of superantigen in the etiology of KD. Our preliminary analysis of 19 patients meeting clinical criteria for KD, as well as studies from other centers, suggests that a superantigen might play a role in some, but not all, patients. Further studies in a larger patient group is necessary before a conclusion can be reached; the studies outlined in this proposal will add the analysis of an anticipated additional 20 KD patients admitted to the Children's Hospital in Cincinnati during the next year. Flow cytometry will be used to analyze peripheral blood lymphocytes (PBL) at presentation and at convalescence (6 weeks), for expansion of specific Vbeta families of T cell receptors (TCR), as well as for expression of the activation markers IL-2 receptor and HLA-DR, and the memory marker CD45RO. mRNA from PBL will also be analyzed by polymerase chain reaction (PCR) for those Vbeta families which cannot be studied by flow cytometry (due to the unavailability of specific monoclonal antibodies). Additional studies will determine the cell populations involved in coronary arteritis in an animal model of vasculitis with some similarities to KD induced by the administration of Lactobacillus casei (L. casei) cell wall extract. These studies will determine whether L. casei contains superantigens which are responsible for this disease, the cell population(s) responsible for vasculitis, whether TCR expression in the vasculitic lesions differs from that in the periphery, and whether T cells in the vasculitic lesions are clonal or polyclonal in nature. These studies should lead to a clarification of the potential role of superantigen in the etiology of KD resulting in a better understanding of the pathophysiology of this important childhood illness.

Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Cincinnati Children's Hospital Medical Center
Department
Type
DUNS #
071284913
City
Cincinnati
State
OH
Country
United States
Zip Code
45229
Thornton, Sherry; Sowders, Dawn; Aronow, Bruce et al. (2002) DNA microarray analysis reveals novel gene expression profiles in collagen-induced arthritis. Clin Immunol 105:155-68
Scola, Michael P; Thompson, Susan D; Brunner, Hermine I et al. (2002) Interferon-gamma:interleukin 4 ratios and associated type 1 cytokine expression in juvenile rheumatoid arthritis synovial tissue. J Rheumatol 29:369-78
Thornton, S; Kuhn, K A; Finkelman, F D et al. (2001) NK cells secrete high levels of IFN-gamma in response to in vivo administration of IL-2. Eur J Immunol 31:3355-60
Griffin, T A; Slack, J P; McCluskey, T S et al. (2000) Identification of proteassemblin, a mammalian homologue of the yeast protein, Ump1p, that is required for normal proteasome assembly. Mol Cell Biol Res Commun 3:212-7
Thornton, S; Boivin, G P; Kim, K N et al. (2000) Heterogeneous effects of IL-2 on collagen-induced arthritis. J Immunol 165:1557-63
Lovell, D J; Giannini, E H; Reiff, A et al. (2000) Etanercept in children with polyarticular juvenile rheumatoid arthritis. Pediatric Rheumatology Collaborative Study Group. N Engl J Med 342:763-9
Hashkes, P J; Balistreri, W F; Bove, K E et al. (1999) The relationship of hepatotoxic risk factors and liver histology in methotrexate therapy for juvenile rheumatoid arthritis. J Pediatr 134:47-52
Lovell, D J; Lindsley, C B; Rennebohm, R M et al. (1999) Development of validated disease activity and damage indices for the juvenile idiopathic inflammatory myopathies. II. The Childhood Myositis Assessment Scale (CMAS): a quantitative tool for the evaluation of muscle function. The Juvenile Dermatomyositis D Arthritis Rheum 42:2213-9
Murray, K J; Grom, A A; Thompson, S D et al. (1998) Contrasting cytokine profiles in the synovium of different forms of juvenile rheumatoid arthritis and juvenile spondyloarthropathy: prominence of interleukin 4 in restricted disease. J Rheumatol 25:1388-98
Sleight, B J; Prasad, V S; DeLaat, C et al. (1998) Correction of autoimmune lymphoproliferative syndrome by bone marrow transplantation. Bone Marrow Transplant 22:375-80

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