S1P receptor modulators are described as drugs that target the S1P-S1P receptor axis in neurological, autoimmune, and inflammatory disorders. In MS, their main pharmacologic effect is induction of lymphopenia through loss of responsiveness to S1P gradients that guide lymphocyte egress.
First-pass extracted concept
S1P receptor modulators
Aliases
sphingosine 1-phosphate receptor modulators
Extracted Explainers
What the tool is doing
What problem it solves
What it does not solve
Evidence Snippets
The relevance of S1P-S1P receptor axis in the pathophysiology of immune and nervous systems has encouraged the development of S1P receptor modulators for the treatment of neurological, autoimmune and/or inflammatory disorders. Currently, four S1P receptor modulators are approved drugs for multiple sclerosis (MS).
Supporting Sources
Linked Claims
S1P receptor modulators may cross the blood-brain barrier and directly target CNS resident cells expressing S1P receptors.
Further, these drugs may cross the blood-brain barrier and directly target CNS resident cells expressing S1P receptors.
The main pharmacologic effect of S1P receptor modulators in MS is induction of lymphopenia by causing loss of responsiveness to S1P gradients that guide lymphocyte egress from lymphoid organs into the bloodstream.
As main pharmacologic effect, these treatments induce lymphopenia due to the loss of responsiveness to S1P gradients guiding lymphocyte egress from lymphoid organs into the bloodstream.
S1P modulators have immunological effects beyond inhibition of lymphocyte trafficking.
Recent data point to immunological effects of the S1P modulators beyond the inhibition of lymphocyte trafficking.
Four S1P receptor modulators are approved drugs for multiple sclerosis.
Currently, four S1P receptor modulators are approved drugs for multiple sclerosis (MS)
Mechanistic insights from S1P receptor modulators in MS may help direct therapeutic approaches targeting S1P receptors in other disease areas.
These insights can direct the application of therapeutic approaches targeting S1P receptors in other disease areas.