Key result
Selective blockade of potassium channels KCa3.1 and Kv1.3 holds promise for modulating inflammatory T and B cells in autoimmune and inflammatory diseases.
Potassium channels KCa3.1 and Kv1.3 are emerging as promising therapeutic targets for immunosuppression in autoimmune and inflammatory diseases.
Recent advances in the biology of potassium channels have raised their profile as therapeutic targets for immunosuppression. Selective blockade of the intermediate-conductance calcium-activated potassium channel KCa3.1, and in particular, the voltage-gated potassium channel, Kv1.3 holds great promise in the modulation of different subsets of inflammatory T cells and B cells involved in the pathogenesis of autoimmune and inflammatory diseases. Relatively few selective blockers of these channels have been discovered to date, but this situation is likely to change as these channels become increasingly prominent as tractable and selective therapeutic targets, and especially if they are clinically validated as immunosuppressive targets.
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Jonathan B. Baell (2005) conducted a review in Autoimmune and inflammatory diseases. Potassium channel blockers (KCa3.1 and Kv1.3) was evaluated. Selective blockade of potassium channels KCa3.1 and Kv1.3 holds promise for modulating inflammatory T and B cells in autoimmune and inflammatory diseases.
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