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Research Article

Uric acid and HMGB1 are involved in the induction of autoantibodies elicited in mice infected with mouse hepatitis virus A59

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Pages 631-640 | Received 19 Nov 2010, Accepted 07 Apr 2011, Published online: 23 May 2011
 

Abstract

We have shown that mice infected with mouse hepatitis virus A59 develop autoantibodies (autoAb) to liver and kidney fumarylacetoacetate hydrolase (FAH). Because it has been proposed that the immune system is stimulated by alarm signals called damage-associated molecular patterns or alarmins, we investigated the participation of uric acid and high-mobility group box protein 1 (HMGB1) in the autoimmune response elicited by mouse hepatitis virus (MHV). Mice subjected to MHV infection had increased plasmatic uric acid concentration that significantly decreased after 20 days of daily treatment with allopurinol and, simultaneously, autoAb to FAH were undetected. Furthermore, this autoAb disappeared after 30 days of treatment with ethyl pyruvate, along with a substantial reduction in serum HMGB1 concentration. Both results indicated a remarkable relationship between the autoimmune process induced by the virus and uric acid and HMGB1 liberation. Unexpectedly, it was found that allopurinol and ethyl pyruvate inhibited the release of both uric acid and HMGB1. Because HMGB1 is activated through binding to interleukin 1β, and that this cytokine is produced by the NLRP3 inflammasome that could be stimulated by uric acid, we propose that both alarmins could be acting in concert with the induction of the autoAb to FAH in MHV-infected mice.

Acknowledgements

The authors are indebted to Dr Pierre L. Masson (de Duve Institute, Université catholique de Louvain, Brussels, Belgium) for helpful discussions and critical revision of the manuscript.

Declaration of Interest: This work was supported by grants from Consejo Nacional de Investigaciones Ciéntificas y Tècnicas (CONICET) [Grant number PIP 096] and Universidad de Buenos Aires, Argentina (UBA) [Grant B057]. The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

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