I found a wonderful write up on Coya's niche- Tregs. I pulled off a tricky move to get this enjoy!
Tregs
Tregs are a specific subset of CD4-positive T cells discovered in 1995 by Prof. Shimon Sakaguchi, who is on Coya's scientific advisory board. They have a heavily regulatory function in maintaining homeostasis, a state of balance needed for the body to function correctly, in the immune system. Their deletion and dysfunction triggers severe inflammation and development of autoimmune diseases. Tregs have strong immunomodulatory properties in different diseases, for example by inhibiting T cell-mediated immune responses against self-antigens, as a protection against autoimmunity.
They are also found in the brain, where they regulate immune response directly or through bystander suppression / signaling to brain-resident immune cells such as microglia and astrocytes. The implication of CNS immune dysfunction in a wide array of neurodegenerative diseases is recognized for two reasons: their main function is to nurture and sculpt the brain, but they have been seen to create an inflammatory loop in neurodegenerative diseases which no longer seems to allow them to perform their normal function, leading to neurodegeneration.

Treg function in the CNS(Source: Immunology Letters, Brain-resident regulatory T cells and their role in health and disease, A. Liston, J. Dooley, L. Yshii)
Total and resting Tregs are significantly decreased and dysfunctional in neurodegenerative diseases such as Alzheimer's and ALS. Coya showed that Treg dysfunction seems to drive neurodegeneration across neurodegenerative diseases. Tregs are reduced in numbers and function in neurodegenerative diseases. More reduction seems associated with more rapid disease progression.

Treg dysfunction in ALS(Corporate Presentation)
Inflammation and immune function can be regulated by Tregs. For utmost efficacy, someconsiderthat both Treg function should be activated and suppressing T-effector function lowered. Teffs counterbalance Tregs.
Coya 301 modulates Tregs and suppresses Teffs. Coya 302 is a further version adding in a macrophage/microglia suppressor.
- In ALS, patients who normally progressed 13.2 points over a year's time on a 48-point scale became practically progression free over 48 weeks with Coya 302 treatment.
-
Coya 302's results stand out
The average life expectancy of ALS patients is 2 to 5 years, with 50% dying within 2.5 years after symptoms onset, which shows just how devastating this disease is.
Post-treatment with Coya 302, patients' normal ALS progression seemed to return, suggesting treatment efficacy.
Coya 302 essentially gave patients who were on a 2-5 year trajectory to death an extra year of no decline. The results also suggest that efficacy could have been continued if treatment would have continued.
This article was written by

E. Roudasev<--- PROPS. WELL DONE!
>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>> & that was the tiny bit of news that I caught whiff of yesterday... the trial
continues to show survival & it looks like you MUST stay on the drug forever.... BUT HAVE WE FINALLY FOUND AN ALS TRTEATMENT THAT WORKS!
AND WHAT HAPPENS WHEN WE START APPLYING THIS TO OTHER AUTO IMMUNE DISEASES....---->
ULTIMATE TARGET $24>
Tregs
Tregs are a specific subset of CD4-positive T cells discovered in 1995 by Prof. Shimon Sakaguchi, who is on Coya's scientific advisory board. They have a heavily regulatory function in maintaining homeostasis, a state of balance needed for the body to function correctly, in the immune system. Their deletion and dysfunction triggers severe inflammation and development of autoimmune diseases. Tregs have strong immunomodulatory properties in different diseases, for example by inhibiting T cell-mediated immune responses against self-antigens, as a protection against autoimmunity.
They are also found in the brain, where they regulate immune response directly or through bystander suppression / signaling to brain-resident immune cells such as microglia and astrocytes. The implication of CNS immune dysfunction in a wide array of neurodegenerative diseases is recognized for two reasons: their main function is to nurture and sculpt the brain, but they have been seen to create an inflammatory loop in neurodegenerative diseases which no longer seems to allow them to perform their normal function, leading to neurodegeneration.

Treg function in the CNS(Source: Immunology Letters, Brain-resident regulatory T cells and their role in health and disease, A. Liston, J. Dooley, L. Yshii)
Total and resting Tregs are significantly decreased and dysfunctional in neurodegenerative diseases such as Alzheimer's and ALS. Coya showed that Treg dysfunction seems to drive neurodegeneration across neurodegenerative diseases. Tregs are reduced in numbers and function in neurodegenerative diseases. More reduction seems associated with more rapid disease progression.

Treg dysfunction in ALS(Corporate Presentation)
Inflammation and immune function can be regulated by Tregs. For utmost efficacy, someconsiderthat both Treg function should be activated and suppressing T-effector function lowered. Teffs counterbalance Tregs.
Coya 301 modulates Tregs and suppresses Teffs. Coya 302 is a further version adding in a macrophage/microglia suppressor.
- In ALS, patients who normally progressed 13.2 points over a year's time on a 48-point scale became practically progression free over 48 weeks with Coya 302 treatment.
-
Coya 302's results stand out
The average life expectancy of ALS patients is 2 to 5 years, with 50% dying within 2.5 years after symptoms onset, which shows just how devastating this disease is.
Post-treatment with Coya 302, patients' normal ALS progression seemed to return, suggesting treatment efficacy.
Coya 302 essentially gave patients who were on a 2-5 year trajectory to death an extra year of no decline. The results also suggest that efficacy could have been continued if treatment would have continued.
This article was written by

E. Roudasev<--- PROPS. WELL DONE!
>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>> & that was the tiny bit of news that I caught whiff of yesterday... the trial
continues to show survival & it looks like you MUST stay on the drug forever.... BUT HAVE WE FINALLY FOUND AN ALS TRTEATMENT THAT WORKS!
AND WHAT HAPPENS WHEN WE START APPLYING THIS TO OTHER AUTO IMMUNE DISEASES....---->
ULTIMATE TARGET $24>
8:02 AM