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Identification of Myelin Basic Proteins in Circulating Immune Complexes Associated with Lepromatous Leprosy
- Source :
- Clinical Immunology and Immunopathology (Now Called Clinical Immunology); April 1994, Vol. 71 Issue: 1 p38-43, 6p
- Publication Year :
- 1994
-
Abstract
- Circulating immune complexes (CIC) were first measured in lepromatous patients (LL) by the <SUP>125</SUP>I-C<SUB>1</SUB>q binding assay and the polyethylene glycol (PEG) precipitation test. High levels were found by both methods (95 and 90% of positives, respectively). LL-CIC were investigated for the presence of neural antigens. CIC were precipitated in 3.5% PEG, filtered through protein A-Sepharose affinity chromatography, eluted with glycine-HCI, pH 2.8, and washed with PBS; fractions after CIC dissociation were studied by SDS-PAGE and Western blotting. The LL-CIC PEG precipitates and the glycine-HCI eluates were positive in 76 and 71% respectively against anti-myelin basic proteins (MBP) monoclonal antibody, showing a single band at 15-25 kDa similar to the one obtained incubating MBP with anti-MBP. No reaction was detected with CIC-PBS fractions; strips were incubated with other anti-neural antibodies such as anti-glial fibrillary acidic proteins, anti-S-100, and anti-neuarofilaments, without any reactivity. Our results demonstrate that LL-CIC contain MBP as an antigen; its significance could be related to the pathogenesis of leprosy since the liberation of MBP after Mycobacterium leprae nerve damage may elicit anti-MBP autoantibodies to myelin breakdown, which reacts with peripheral nerve MBP inducing CIC formation. This mechanism may be important in demyelination and destruction of nerve in leprosy. Copyright 1994, 1999 Academic Press
Details
- Language :
- English
- ISSN :
- 00901229 and 10902341
- Volume :
- 71
- Issue :
- 1
- Database :
- Supplemental Index
- Journal :
- Clinical Immunology and Immunopathology (Now Called Clinical Immunology)
- Publication Type :
- Periodical
- Accession number :
- ejs727938
- Full Text :
- https://doi.org/10.1006/clin.1994.1049