Abstract
In human T-lymphocytes, the voltage-gated Kv1.3 channel and the Ca(2+)-activated IKCa1 channel play an important role in Ca2+ signaling, activation, adhesion and migration and have, therefore, long been regarded as attractive targets for immunotherapy. Here, we review the pharmacology of the two channels, their expression pattern in naïve and memory T-cells and their functional roles during T-cell activation, and explain the rationale for the use of Kv1.3 blockers for the therapy of T-cell mediated autoimmune diseases.
MeSH terms
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Humans
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Intermediate-Conductance Calcium-Activated Potassium Channels
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Kv1.3 Potassium Channel
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Lymphocyte Activation / immunology
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Multiple Sclerosis / drug therapy*
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Multiple Sclerosis / immunology
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Phenotype
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Potassium Channel Blockers / pharmacology*
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Potassium Channel Blockers / therapeutic use
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Potassium Channels / metabolism*
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Potassium Channels, Voltage-Gated*
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T-Lymphocytes / drug effects
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T-Lymphocytes / immunology
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T-Lymphocytes / metabolism
Substances
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Intermediate-Conductance Calcium-Activated Potassium Channels
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KCNA3 protein, human
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KCNN4 protein, human
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Kv1.3 Potassium Channel
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Potassium Channel Blockers
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Potassium Channels
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Potassium Channels, Voltage-Gated