Cross-reactivity of anti-galactocerebroside autoantibodies with a Trypanosoma brucei proteolipidic epitope
Article first published online: 24 DEC 2001
DOI: 10.1046/j.1365-2249.2000.01166.x
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How to Cite
Girard, M., Bisser, S., Buscher, P., Bouteille, B., Preud’Homme, J.-L. and Jauberteau, M.-O. (2000), Cross-reactivity of anti-galactocerebroside autoantibodies with a Trypanosoma brucei proteolipidic epitope. Clinical & Experimental Immunology, 119: 516–522. doi: 10.1046/j.1365-2249.2000.01166.x
Publication History
- Issue published online: 24 DEC 2001
- Article first published online: 24 DEC 2001
- (Accepted for publication 23 November 1999)
- Abstract
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Keywords:
- galactocerebrosides;
- autoantibodies;
- molecular mimicry;
- Trypanosoma brucei
Pathogenic mechanisms of the demyelinating encephalopathy featuring the nervous phase of human African trypanosomiasis (HAT) are largely unknown. They might include autoimmune disorders. A variety of autoantibodies is detected during the disease and we have previously evidenced anti-galactocerebroside (GalC) antibodies in the serum and cerebrospinal fluid (CSF) from patients in the nervous stage (stage II) of HAT. We now show that anti-GalC antibodies recognize an antigen located on the parasite membrane and common to different strains of trypanosomes. By using affinity chromatography with a rabbit anti-GalC antiserum, a 52-kD proteolipid was isolated from the membrane of Trypanosoma brucei (T. b.) brucei AnTat 1.9, AnTat 1.1E, and T. b. rhodesiense Etat 1.2/R and Etat 1.2/S. Antibodies directed against this antigen were found in the CSF from patients with nervous stage HAT. These CSF also contained anti-GalC antibodies and adsorption with the proteolipid decreased anti-GalC reactivity. Immunization of mice with this antigen induced the production of antibodies which cross-reacted with GalC but no protection from experimental infection with T. b. brucei. These data support the hypothesis that anti-GalC antibodies detected in the CSF from HAT patients might be induced by molecular mimicry with a parasite antigen.

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