Nerve and skin damage in leprosy is associated with increased intralesional heat shock protein

• Published in: Clinical and experimental immunology 1994-05, Vol.96 (2), p.208-213
• Main Authors: KHANOLKAR‐YOUNG, S., YOUNG, D. B., COLSTON, M. J., STANLEY, J. N. A., LOCKWOOD, D. N. J.
• Format: Article
• Language: English
• Subjects: Bacterial diseases; Biological and medical sciences; Biopsy; heat shock protein; Heat-Shock Proteins - isolation & purification; Human bacterial diseases; Humans; immunocytochemistry; Immunohistochemistry; Infectious diseases; Leprosy; Leprosy - pathology; Medical sciences; Mycobacterium leprae; peripheral nerve; Peripheral Nerves - chemistry; Peripheral Nerves - pathology; Skin - chemistry; Skin - pathology; Tissue Distribution; Tropical bacterial diseases
• ISSN: 0009-9104; 1365-2249
• DOI: 10.1111/j.1365-2249.1994.tb06543.x

SUMMARY Leprosy is frequently complicated by the development of reversal reactions in which peripheral nerve and skin lesions become inflamed and irreversible nerve damage may ensue. Increased expression of proteins belonging to the 70‐kD heat shock family (hsp70) occurs in cells of the central nervous system exposed to hyperthermia, physical damage or drug‐induced trauma. In the present study we have used immunocytochemical staining to monitor hsp70 levels in peripheral nerves infected by Mycobacterium leprae. Hsp70 was detected in skin and nerve lesions from all leprosy patients, but was particularly prominent in lesions from patients undergoing reversal reactions. Hsp70 immunocytochemistry can thus be used as a marker of neural injury in the peripheral as well as in the central nervous system. The cellular dynamics of nerve damage in leprosy are currently poorly understood, and we postulate that the immunopathology of leprosy may be partly due to an autoimmune response to heat shock proteins.