Abstract
Genetic associations with autoimmune disease are enriched in immune response regulators. The immune system in individuals at genetic risk of autoimmunity must balance pressures on the innate and adaptive immune system, most notably infection control, with those of maintaining self-tolerance or controlling autoimmune inflammation. In spite of multiple tolerance mechanisms, inflammation becomes chronic in autoimmune disease, and complete resolution is difficult. This article proposes a perspective on the pathogenesis of autoimmunity—focusing on rheumatoid arthritis and type 1 diabetes—integrating clinical advances and animal models with the role that colonizing micro-organisms play in the balance between tolerance and autoimmunity.
ACKNOWLEDGMENTS
Ranjeny Thomas is supported by Arthritis Queensland and by grants from JDRF, NHMRC, and the Princess Alexandra Hospital Foundation. I thank Saparna Pai, Brendan O’Sullivan, Merja Ruutu, Andrew Cotterill, and Mark Harris for helpful discussions.
Declaration of Interest: The author reports no conflicts of interest. The author alone is responsible for the content and writing of the paper.