Autoantibodies to human stress proteins

Submitted by Naturenomics Team on Tue, 29/11/2016 - 08:59
Abstract

Unselected sera from patients with various rheumatic, inflammatory bowel, and autoimmune skin diseases (n=268) were examined against human cell lysate by immunoblotting procedures, to determine the prevalence of autoantibodies to stress proteins (heat-shock proteins) hsp60 (homolog of Escherichia coli groEL and Mycobacterial 65K antigens), hsp73, and hsp90.  Using standard, sensitive and specific assay conditions, IgG and IgM autoantibodies to these stress proteins were not demonstrable, or were detected infrequently, in sera from control subjects (n=36) and from patients with rheumatoid arthritis, Sjogren's syndrome, ankylosing spondylitis, Reiter's syndrome, systemic lupis erythematosus, and systemic sclerosis.  Autoantibodies to hsp60 were relatively more common (>= 20% of sera) in patients with mixed connective tissue disease, polymyositis/dermatomyositis, psoriatic arthritis, inflammatory bowel disease, epidermolysis bullosa acquista, and bullous pemphigoid.  Anti-hsp73 autoantibodies were detected in 20% or more of the sera from patients were Lyme disease and ulcerative colitis.  Taken together, these data extend the spectrum of autoimmune and inflammatory diseases in which humoral anti-stress protein reactivity develops.  However, the paucity of humoral autoreactivity to stress proteins in patients with systemic lupis erythematosus and rheumatoid arthritis argues against a direct role of anti-stress protein autoantibodies in the pathogenesis of these disorders.

Author

Jarjour, W.N., Jeffries, B.D., Davis, J.S., Welch, W.J., Mimura, T., Winfield, J.B., 1991. 

References

 Arthritis and Rheumatism 34, 1133-1138

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