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Editorial
. 2018 Mar 30;122(7):911-912.
doi: 10.1161/CIRCRESAHA.118.312860.

Complementing T Regulatory Cells to Combat Hypertension

Affiliations
Editorial

Complementing T Regulatory Cells to Combat Hypertension

Keisa W Mathis. Circ Res. .
No abstract available

Keywords: Editorials; blood pressure; complement activation; forkhead transcription factors; hypertension; inflammation.

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Figures

Figure 1
Figure 1. Therapeutic applicability of enhancing T regulatory cells
There is strong evidence that blockade of complement activation product signaling through the C3a receptor (C3aR) and C5aR enhances the anti-inflammatory function of T regulatory cells (Tregs). Other mechanisms have also been effective in augmenting Tregs. For example, activation of a particular neuroimmune axis (termed the cholinergic anti-inflammatory pathway) via vagus nerve stimulation increases Tregs. In addition, in vivo stimulation of Tregs using an anti-CD28 superagonistic monoclonal antibody, and ex vivo/in vitro stimulation via anti-CD28/CD3 monoclonal antibody-coated beads both are known to modulate Tregs. Because the reduction of Tregs is usually pathogenic and because adoptive transfer of Tregs has been shown to be therapeutic, it is important to effectively optimize methods to enhance Tregs to potentially combat chronic inflammatory disorders with oxidative stress including renal diseases, vascular diseases, and importantly, hypertension.

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References

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