The molecular mechanism that drives the disease-causing effects of the most common genetic risk factor for lupus, HLA-DRB1*03:01, has been revealed in
a new study.
Systemic lupus erythematosus is a common, incurable autoimmune disease that affects millions of individuals worldwide, with a particularly high prevalence among women. The genetic variant HLA-DRB1*03:01 is the greatest risk factor for the condition, which involves inflammation in many vital organs, and can lead to severe disability and death.
In the study, investigators found that a protein coded by that HLA variant triggers a cascade of molecular and cellular effects that can cause the inflammatory symptoms seen in lupus patients.