The Challenge With Today’s Autoimmune Treatments
Most therapies for autoimmune diseases focus on easing symptoms or lowering inflammation. While helpful, they often don’t address the underlying immune dysfunction, require continuous use, and primarily target IgG antibodies, even though many diseases also involve IgA and IgM.
As a result, patients may experience incomplete or short-lived improvement.
The Biology Driving Autoimmune Disease
In conditions like generalized myasthenia gravis and primary Sjögren’s disease, overactive B cells produce harmful antibodies that attack healthy tissues. Two signaling proteins, BAFF and APRIL, fuel this overactivity by helping B cells grow, survive, and produce these autoantibodies.
When BAFF and APRIL are elevated, the immune system can become stuck in a cycle of ongoing B-cell activation and antibody production.
How Telitacicept Creates a Different Outcome
Telitacicept blocks both BAFF and APRIL, helping rebalance B-cell activity at its source. By reducing the survival signals that drive harmful antibody production, it has the potential to:
- Lower disease-causing IgG, IgA, and IgM antibodies
- Modulate disease-relevant antibody pathways
- Avoid broad immune suppression by modulating, not depleting, B cells
This approach is being investigated to better understand how targeting upstream pathways may influence disease biology.