A targeted treatment option for psoriasis
Treatment options for psoriasis — one of the most common chronic inflammatory skin diseases — have previously focused on inhibiting pro-inflammatory immune cells. Now a new study led by the Medical University of Vienna has shown that it is possible to restore the function of certain anti-inflammatory immune cells in a targeted manner, paving the way for the development of a therapy that not only works more precisely but is also associated with fewer side effects.
The research team focused its investigations on the role of regulatory T cells (Treg cells) in chronic inflammatory skin diseases such as psoriasis. Treg cells are important components of the body’s immune system that specialise in preventing excessive immune responses and thus inflammation.
It is already known that Treg cells lose their regulatory function in chronic skin inflammation, causing the immune response to become uncontrolled and the disease to progress. The researchers have now decoded the exact mechanism behind this for the first time, with their results published in the journal Immunity.
“We were able to show that the loss of the anti-inflammatory function of regulatory T cells is caused by a malfunction of the cellular metabolism,” said study leader Georg Stary.
As the researchers’ analysis revealed, the enzyme SSAT plays a key role in the loss of function of Treg cells. SSAT is involved in the regulation of certain molecules (polyamines) that are important for the balance between anti-inflammatory and pro-inflammatory immune cells. If SSAT is produced in increased amounts in Treg cells, they lose their regulatory function and begin to produce pro-inflammatory messenger substances themselves. This fuels the excessive immune response typical of psoriasis.
With the key role of SSAT in the inflammatory process, the researchers have discovered a new starting point for therapy. In a mouse model with psoriasis-like skin inflammation, it was shown that inhibiting SSAT can restore the regulatory function of Treg cells and break the cycle of inflammation. Thus, the development of specific drugs that specifically inhibit SSAT could represent a promising alternative to existing treatment approaches, which are often associated with immunosuppression and increased susceptibility to infection.
“Since other chronic inflammatory diseases of the skin or other organs are also characterised by impaired immune regulation, our approach could be important beyond psoriasis,” Stary concluded.
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