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JACC Basic Transl Sci. 2017 Aug 28;2(4):418-430. doi: 10.1016/j.jacbts.2017.06.005. eCollection 2017 Aug.

The IL-1β Antibody Gevokizumab Limits Cardiac Remodeling and Coronary Dysfunction in Rats With Heart Failure.

JACC. Basic to translational science

Najah Harouki, Lionel Nicol, Isabelle Remy-Jouet, Jean-Paul Henry, Anais Dumesnil, Annie Lejeune, Sylvanie Renet, Francesca Golding, Zoubir Djerada, Didier Wecker, Virginie Bolduc, Muriel Bouly, Jerome Roussel, Vincent Richard, Paul Mulder

Affiliations

  1. INSERM U1096, Rouen, France.
  2. Normandy University, IRIB, Rouen, France.
  3. Unité de formation et de recherche de Médecine et Pharmacie, Rouen University, Rouen, France.
  4. Plateau d'Imagerie CardioThoracique de l'Université de Rouen, Rouen, France.
  5. Pharmacology Department, Centre Hospitalier Universitaire de Reims, Reims, France.
  6. Bruker Biospin MRI GMBH, Ettlingen, Germany.
  7. Institut de Recherches Internationales Servier, Suresnes, France.

PMID: 30062160 PMCID: PMC6034492 DOI: 10.1016/j.jacbts.2017.06.005

Abstract

This study reports preclinical data showing that the interleukin (IL)-1β modulation is a new promising target in the pathophysiological context of heart failure. Indeed, in nondiabetic Wistar and diabetic Goto-Kakizaki rats with chronic heart failure induced by myocardial infarction, administration of the IL-1β antibody gevokizumab improves 'surrogate' markers of survival (i.e., left ventricular remodeling, hemodynamics, and function as well as coronary function). However, whether IL-1β modulation per se or in combination with standard treatments of heart failure improves long-term outcome in human heart failure remains to be determined.

Keywords: GK, Goto-Kakisaki; I/R, ischemia/reperfusion; IL, interleukin; IL-1β; LV, left ventricle/ventricular; LVEDP, left ventricular end-diastolic pressure; LVEDPV, left ventricular end-diastolic pressure–volume relationship; LVESP, left ventricular end-systolic pressure; LVESPVR, left ventricular end-systolic pressure–volume relationship; ROS, reactive oxygen species; SOD, superoxide dismutase; cardiovascular function; heart failure; ischemia/reperfusion

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