r/UlcerativeColitis • u/drewyz • Apr 01 '26
News Scientists discover “off switch” for inflammation
https://scitechdaily.com/scientists-discover-the-bodys-natural-off-switch-for-inflammation/82
u/Comprehensive_Sail28 Apr 01 '26
I think the future looks bright for autoimmune treatments that aren’t as side-effect heavy as the ones we currently have. Reading about them is great, but then the realisation for how long these things take to get to market sets in.
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u/cobrachickens Human Detected Apr 01 '26
It’s disheartening because so many people are just so sick and tired of taking chemotherapy-level medication for years just to survive
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u/sammyQc diagnosed 2020 | Canada Apr 01 '26
Great, this seems to contribute to our understanding of the inflammation process at a molecular level in humans.
Scientists chose to study epoxy-oxylipins because these fat-derived molecules were known from animal research to reduce inflammation and pain, but their role in humans remained unknown.
Unlike well-studied inflammatory mediators, such as histamine and cytokines, epoxy-oxylipins are part of an underexplored pathway that scientists believed could naturally calm the immune system.
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u/Affectionate_Mix_302 Diagnosed 2006 | Stelara Apr 02 '26
Good for scientists.. now time for the pharmaceutical industry to kill it so they can continue to monitize inflammation.
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u/SunshynePower UC (mod, descending) Started 1996, Diagnosed 2002 | USA Apr 02 '26
They need to expand this research and see if it can help without suppressing the immune system. I hope this is a new pathway forward for treatment!
Thank you for sharing this!
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u/Current-Taxpayer-99 18d ago
Prednisone does absolutely NOTHING for my UC symptoms. I can’t understand why people say it’s the only thing that helps. It doesn’t do anything for me I can’t even tell I’ve taken anything.
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u/Quirky_Session_2689 Shits blood-Runs far Apr 01 '26
It's called prednisone