Increased toll-like receptor 4 in the myocardium of patients requiring left ventricular assist devices

J Heart Lung Transplant. 2004 Feb;23(2):228-35. doi: 10.1016/S1053-2498(03)00106-2.

Abstract

Background: Cytokine activation in the myocardium of deteriorating patients with heart failure who undergo left ventricular assist-device (LVAD) implantation has been documented, but the underlying mechanisms remain poorly understood. We hypothesized the innate immune system is activated with expression of Toll-like receptor 4 (TLR4), leading to cytokine activation in these patients.

Methods: We used quantitative real-time reverse-transcriptase polymerase chain reaction to measure TLR4, interleukin-1 (IL-1) receptor, IL-1 beta, IL-6, and tumor necrosis factor alpha (TNF-alpha) mRNA expression in myocardial samples from 36 patients. We compared 18 patients who underwent LVAD implantation with 18 patients with less severe heart failure who underwent elective heart transplantation.

Results: Toll-like receptor 4 expression was 1.69-fold greater (p < 0.05) and IL-1 receptor expression was 3.64-fold greater (p < 0.0001) in the deteriorating patients who required LVADs. Myocardial TNF-alpha (1.71-fold, p < 0.05), IL-6 (2.57-fold, p < 0.005), and IL-1 beta (9.78-fold, p < 0.001) also were increased in the LVAD candidates. Toll-like receptor 4 expression correlated strongly with IL-1 receptor expression (r= 0.75, p < 0.0001) and with IL-1 beta expression in individual patients (r = 0.7, p < 0.0001). Interleukin-1 receptor expression also correlated with IL-1 beta expression (r = 0.78, p < 0.0001) within patients. We found no correlation between TLR4 and either TNF-alpha or IL-6 expression.

Conclusions: Patients who required LVAD support showed evidence of innate immune system activation, indicated by an increase in the key effector molecule TLR4 associated with a specific pattern of cytokine expression in the myocardium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cytokines / metabolism*
  • Female
  • Heart Failure / immunology*
  • Heart Failure / therapy
  • Heart-Assist Devices*
  • Humans
  • Interleukin-1 / immunology
  • Interleukin-6 / immunology
  • Male
  • Membrane Glycoproteins / immunology*
  • Myocardium / immunology*
  • RNA, Messenger / genetics
  • Receptors, Cell Surface / immunology*
  • Receptors, Interleukin-1 / immunology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Toll-Like Receptor 4
  • Toll-Like Receptors
  • Tumor Necrosis Factor-alpha / immunology

Substances

  • Cytokines
  • Interleukin-1
  • Interleukin-6
  • Membrane Glycoproteins
  • RNA, Messenger
  • Receptors, Cell Surface
  • Receptors, Interleukin-1
  • TLR4 protein, human
  • Toll-Like Receptor 4
  • Toll-Like Receptors
  • Tumor Necrosis Factor-alpha