The Ca2 Channel Blocker Verapamil Inhibits the In Vitro Activation and Function of T Lymphocytes: A 2022 Reappraisal
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Ca2 channel blockers (CCBs) are commonly used to treat different cardiovascular conditions. These drugs disrupt the intracellular Ca2 signaling network, inhibiting numerous cellular functions in different cells, including T lymphocytes. We explored the effect of the CCB verapamil on normal human peripheral blood T cell activation, proliferation, and cytokine production. Cells were activated by ligating CD3 or CD3/CD28 in the presence or absence of verapamil, and the expression of activation-induced cell surface molecules (CD25, CD40L, CD69, PD-1, and OX40), cell proliferation, and cytokine release were assessed by flow cytometry. Verapamil exerted a dose-dependent inhibitory effect on the expression of all the activation-induced cell surface molecules tested. In addition, verapamil diminished T cell proliferation induced in response to CD3/CD28 stimulation. Likewise, the production of Th1/Th17 and Th2 cytokines was also reduced by verapamil. Our data substantiate a potent in vitro suppressive effect of verapamil on T lymphocytes, a fact that might be relevant in patients receiving CCBs. © 2022 by the authors.
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Ca2%2b channel blockers (CCBs) are commonly used to treat different cardiovascular conditions. These drugs disrupt the intracellular Ca2%2b signaling network, inhibiting numerous cellular functions in different cells, including T lymphocytes. We explored the effect of the CCB verapamil on normal human peripheral blood T cell activation, proliferation, and cytokine production. Cells were activated by ligating CD3 or CD3/CD28 in the presence or absence of verapamil, and the expression of activation-induced cell surface molecules (CD25, CD40L, CD69, PD-1, and OX40), cell proliferation, and cytokine release were assessed by flow cytometry. Verapamil exerted a dose-dependent inhibitory effect on the expression of all the activation-induced cell surface molecules tested. In addition, verapamil diminished T cell proliferation induced in response to CD3/CD28 stimulation. Likewise, the production of Th1/Th17 and Th2 cytokines was also reduced by verapamil. Our data substantiate a potent in vitro suppressive effect of verapamil on T lymphocytes, a fact that might be relevant in patients receiving CCBs. © 2022 by the authors.
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Ca2 channel blockers; cytokine production; immunosuppression; T cell activation; verapamil calcium channel; CD134 antigen; CD28 antigen; CD3 antigen; CD40 ligand; CD69 antigen; interleukin 2 receptor alpha; programmed death 1 receptor; verapamil; Article; cell surface; controlled study; cytokine production; cytokine release; dose response; flow cytometry; human; human cell; immunostimulation; immunosuppressive treatment; in vitro study; lymphocyte proliferation; peripheral blood mononuclear cell; protein expression; T lymphocyte activation; Th1 cell; Th17 cell; Th2 cell
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Ca2+ channel blockers; cytokine production; immunosuppression; T cell activation; verapamil calcium channel; CD134 antigen; CD28 antigen; CD3 antigen; CD40 ligand; CD69 antigen; interleukin 2 receptor alpha; programmed death 1 receptor; verapamil; Article; cell surface; controlled study; cytokine production; cytokine release; dose response; flow cytometry; human; human cell; immunostimulation; immunosuppressive treatment; in vitro study; lymphocyte proliferation; peripheral blood mononuclear cell; protein expression; T lymphocyte activation; Th1 cell; Th17 cell; Th2 cell
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