Complement Activation in Patients With Congestive Heart Failure
- 25 September 2001
- journal article
- clinical trial
- Published by Wolters Kluwer Health in Circulation
- Vol. 104 (13) , 1494-1500
- https://doi.org/10.1161/hc3801.096353
Abstract
Background Increasing evidence implicates innate immunity in the pathogenesis of congestive heart failure (CHF). In the present study, we examined the possible role of complement, an important part of innate immunity, in CHF. Methods and Results Complement activation was analyzed in systemic and coronary circulation in 39 patients with CHF and 20 healthy control subjects. In a double-blind, placebo-controlled study, we have recently reported that high-dose intravenous immunoglobulin (IVIG) improves left ventricular ejection fraction (LVEF) in these patients. To examine if this improvement was related to IVIG-induced effects on complement, we also examined complement activation during induction (first week) and maintenance therapy (6 months) with IVIG or placebo. Our main findings were: (1) We found enhanced systemic complement activation involving classic, alternative, as well as terminal pathway in patients with CHF compared with healthy control subjects. (2) Particularly enhanced complement activation was found in coronary sinus, representing venous drainage from the heart. (3) The systemic complement activation was further enhanced during IVIG but not during placebo therapy, particularly during induction therapy. (4) Although IVIG improved LVEF in patients with CHF, the degree of IVIG-mediated complement activation was negatively correlated with this improvement of LVEF. Conclusions This study further supports the involvement of innate immunity in the pathogenesis of CHF. Our findings suggest that complement may be added to the list of possible therapeutic targets in CHF and that future studies with specific complement inhibitors may be of interest in this disorder.Keywords
This publication has 26 references indexed in Scilit:
- Cytokines as Emerging Targets in the Treatment of Heart FailureTrends in Cardiovascular Medicine, 2000
- Complement Activation after Oxidative StressThe American Journal of Pathology, 2000
- Toll4 (TLR4) expression in cardiac myocytes in normal and failing myocardiumJournal of Clinical Investigation, 1999
- Inflammatory Alterations in the Myocardial MicrocirculationJournal of Molecular and Cellular Cardiology, 1998
- High-Dose Intravenous Immunoglobulin Treatment Activates Complement In VivoScandinavian Journal of Immunology, 1998
- A Neoepitope‐Based Enzyme Immunoassay for Quantification of C1‐Inhibitor in Complex with C1r and C1sScandinavian Journal of Immunology, 1997
- Circulating Levels of Cytokines and Their Endogenous Modulators in Patients With Mild to Severe Congestive Heart Failure Due to Coronary Artery Disease or HypertensionJournal of the American College of Cardiology, 1996
- Inhibition of Complement‐Mediated Red Cell Lysis by Immunoglobulins is Dependent on the IG Isotype and its Cl Binding PropertiesScandinavian Journal of Immunology, 1995
- Soluble Human Complement Receptor Type 1: In Vivo Inhibitor of Complement Suppressing Post-Ischemic Myocardial Inflammation and NecrosisScience, 1990
- Quantification in Enzyme‐Linked Immunosorbent Assay of a C3 Neoepitope Expressed on Activated Human Complement Factor C3Scandinavian Journal of Immunology, 1988