Summary
Reactive arthritis is a joint inflammation developing soon after or during an infection elsewhere in the body. A strong association between the development of reactive arthritis and tissue antigen HLA-B27 has been known for a long time. However, it is still unclear by what mechanism(s) this antigen determines the appearance of joint complications. There is considerable evidence that causative micro-organisms or their structures are not efficiently eliminated but persist for long periods of time in patients with reactive arthritis. This suggests that the interaction between micro-organism and host is somehow disturbed in HLA-B27-positive persons developing this complication. The possibility that living micro-organisms persist somewhere in unknown locations in the bodies of patients with reactive arthritis has provided a rationale for antibiotic therapies. In addition, it seems to be clear now that development of reactive arthritis depends on the dissemination of microbial antigens into joints. There they stimulate a local response that could damage joint tissue.
Adequate therapy of reactive arthritis depends on the individual clinical course. In many patients the disease is only of short duration and with a self-limiting character. Symptomatic anti-inflammatory therapy with nonsteroidal anti-inflammatory drugs is often the appropriate treatment. In patients with chronic arthritis, glucocorticoids or even immunosuppressive agents may be administered. Long term therapy with antibiotics seems to be of benefit in patients with uroarthritides caused by, for example, Chlamydia trachomatis. The potential therapeutic impact on enteroarthritides has been up to now less predictable.
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Kellner, H., Granfors, K. Reactive Arthritis. Clin Immunother 4, 338–345 (1995). https://doi.org/10.1007/BF03259297
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DOI: https://doi.org/10.1007/BF03259297