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DOI 10.1073/pnas.89.21.10070

Медицинская библиотека · Proceedings of the National Academy of Sciences of the United States of America · 1992

Human spumaretrovirus-related sequences in the DNA of leukocytes from patients with Graves disease.

Lagaye S, Vexiau P, Morozov V, Guénebaut-Claudet V, Tobaly-Tapiero J, Canivet M, Cathelineau G, Périès J, Emanoil-Ravier R

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Аннотация

Viruses, and more particularly retroviruses, have been postulated to play a role in the pathogenesis of autoimmune diseases. In a search for spumaretrovirus infection markers, we screened a group of 29 patients with Graves disease and a representative healthy population (23 subjects) as a control. Southern blot hybridization under stringent conditions, of patients' DNA extracted from peripheral blood lymphocytes, with a spumaretrovirus-specific genomic probe derived from the human spumaretrovirus (HSRV) prototype, gave a positive signal in 10 cases. Moreover, by PCR, HSRV-related sequences were detected in the DNA of 19 patients (66%). Positive DNA samples in Southern blots were also positive in PCR for all regions tested (gag, bel1, bel2, long terminal repeat). Amplified (gag and bel2) products were cloned and sequenced; they showed high homology with HSRV. On the other hand, all 23 control subjects were negative by both procedures. Sera from both populations were examined for the presence of antibodies reactive with antigens of the spumaretrovirus family. These sera were negative by several immunodetection techniques: ELISA, indirect immunofluorescence, serum neutralization, and Western blotting. These results strongly suggest the existence of an association between Graves disease and the presence of HSRV-related infection markers.

Для цитирования: Lagaye S, Vexiau P, Morozov V, Guénebaut-Claudet V, Tobaly-Tapiero J, Canivet M, Cathelineau G, Périès J, Emanoil-Ravier R. Human spumaretrovirus-related sequences in the DNA of leukocytes from patients with Graves disease.. Proceedings of the National Academy of Sciences of the United States of America. 1992. DOI: 10.1073/pnas.89.21.10070.

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