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Research Article Free access | 10.1172/JCI115801
Department of Dermatology, University of Texas Southwestern Medical Center, Dallas 75235.
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Department of Dermatology, University of Texas Southwestern Medical Center, Dallas 75235.
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Department of Dermatology, University of Texas Southwestern Medical Center, Dallas 75235.
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Department of Dermatology, University of Texas Southwestern Medical Center, Dallas 75235.
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Department of Dermatology, University of Texas Southwestern Medical Center, Dallas 75235.
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Department of Dermatology, University of Texas Southwestern Medical Center, Dallas 75235.
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Department of Dermatology, University of Texas Southwestern Medical Center, Dallas 75235.
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Published June 1, 1992 - More info
We have cloned and sequenced a 46-kD Ro/SS-A autoantigen gene that is the human homologue of the calcium-binding protein, calreticulin. The sequence of this 46-kD Ro/SS-A protein (calreticulin) has significant homology to lambda Ral-1, a recombinant cDNA clone corresponding to a major antigen of the nematode, Onchocerca volvulus, the infectious agent of onchocerciasis. We therefore sought to determine whether antibodies produced by onchocerciasis patients might crossreact with the human 46-kD Ro/SS-A autoantigen (calreticulin). 20 of 22 sera from Liberian onchocerciasis patients who had no known evidence of autoimmune disease were found to contain antibodies that reacted with the 46-kD Ro/SS-A (calreticulin) by immunoblot analysis. Characteristic of sera reactive with Ro/SS-A antigens, some onchocerciasis sera also immunoprecipitated the Ro/SS-A-associated hY RNAs. In addition, a monoclonal antibody raised against O. volvulus organisms reacted to purified human WiL-2 cell 46 kD Ro/SS-A antigen (calreticulin) by ELISA. These results strongly suggest that onchocerciasis patients produce antibodies that crossreact with the 46-kD human Ro/SS-A autoantigen (calreticulin) and raise the possibility that infectious organisms such as O. volvulus might play a triggering or exacerbating role in the human Ro/SS-A autoimmune response.
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