Katherine Deck

Federal Grant PI

Researcher

Last publication 2025 Last refreshed 2026-05-22

faculty

4 h-index 28 pubs 92 cited

Biography and Research Information

OverviewAI-generated summary

Katherine Deck's research focuses on the immunological mechanisms underlying hypertension, particularly the role of T-lymphocytes and specific molecular pathways in its development and progression. Her work investigates how immune cells, such as CD8+ T-cells, interact with other cellular components and signaling molecules to influence blood pressure regulation. Recent publications explore the contribution of interferon-gamma (IFNγ) and its associated pathways, like PD-L1, to the immune-mediated processes driving hypertension. Additionally, her research examines the function of P2X7 receptors in T-cell activation and their role in promoting salt-sensitive hypertension, a condition exacerbated by high dietary sodium intake.

Deck's investigations extend to the kidney and heart, examining how immune responses in these organs contribute to chronic high blood pressure. Her work has identified kidney-resident memory CD8+ T cells as drivers of sustained hypertension and salt sensitivity. She also studies the transition of macrophages to myofibroblasts, a process influenced by cytokines like IL-10, which promotes fibrosis in the failing heart. Her federally funded work, supported by the NIH/National Heart Lung and Blood Institute, specifically targets the role of kidney-resident memory CD8+ T cells in promoting hypertension and memorizing salt sensitivity. Deck collaborates with researchers at the University of Arkansas for Medical Sciences, including Christoph Mora, Shengyu Mu, Yunping Guo, and Tonya Rafferty.

Metrics

  • h-index: 4
  • Publications: 28
  • Citations: 92

Selected Publications

  • IL-10 Drives Macrophage to Myofibroblast Transition Promoting Chronic Fibrosis in the Failing Heart 9287 (2025)
  • Kidney resident-memory CD8+ T cells drive chronic high blood pressure 9288 (2025)
  • Energy Overload: ATP-P2X7-Mediated T Cell Activation in Obesity-Induced Type 2 Diabetes 9286 (2025)
  • Kidney Memory for Salt Sensitivity Resides in T Cells Driving Chronic Hypertension (2025)
  • Uncovering immune pathways for therapeutic targeting of hypertension (2025)
  • Immune Dysregulation Connecting Type 2 Diabetes and Cardiovascular Complications (2025)
  • Cytokine-induced Macrophage Transition Drives Cardiac Fibrosis and Diastolic Dysfunction (2025)
  • Establishment of resident memory T cells anchors hypertension in the kidney (2025)
  • T Cells Drive Kidney Memory for Hypertension (2024)
  • Abstract P200: Immune memory contributes to chronic hypertension recurrence (2024)
  • Abstract P335: An innate immune component in hypertension-induced cardiac dysfunction Christoph Mora, Katherine Deck, Yunmeng Liu, Lance Benson, Tonya Rafferty, & Shengyu Mu (2024)
  • P227 MACROPHAGE TO MYOFIBROBLAST TRANSITION IN THE DEVELOPMENT OF DIASTOLIC DYSFUNCTION (2024)
  • O14 KIDNEY RESIDENT MEMORY T CELLS MEDIATE THE CHRONIC PROGRESSION OF HYPERTENSION (2024)
  • Kidney resident memory CD8 T cells mediate recurrence of salt-sensitive hypertension (2024)
  • Macrophage to Myofibroblast Transition Promotes Hypertension-Induced Cardiac Diastolic Dysfunction (2024)

View all publications on OpenAlex →

Federal Grants 1 $39,509 total

NIH/National Heart Lung and Blood Institute Contact PI Sep 2024 - Sep 2026

Kidney-resident memory CD8+ T cells promote hypertension and memorize salt sensitivity.

National Heart Lung and Blood Institute $39,509 F31

Collaboration Network

29 Collaborators 3 Institutions 1 Country

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