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Circulation. 2001;104:1413-1418
doi: 10.1161/hc3601.095578
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(Circulation. 2001;104:1413.)
© 2001 American Heart Association, Inc.


Basic Science Reports

Inhibition of Mannose-Binding Lectin Reduces Postischemic Myocardial Reperfusion Injury

James E. Jordan, PhD; Michael C. Montalto, PhD; Gregory L. Stahl, PhD

From the Center for Experimental Therapeutics and Reperfusion Injury, Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, Mass.

Correspondence to Dr Gregory L. Stahl, CET&RI, Department of Anesthesia, Brigham and Women’s Hospital, 75 Francis St, Boston, MA 02115. E-mail gstahl{at}zeus.bwh.harvard.edu

Background— Complement consists of a complex cascade of proteins involved in innate and adaptive immunity. The cascade can be activated through 3 distinct mechanisms, designated the classical, alternative, and lectin pathways. Although complement is widely accepted as participating in the pathophysiology of ischemia-reperfusion injury, the specific role of the lectin pathway has not been addressed.

Methods and Results— Monoclonal antibodies (mAbs; P7E4 and 14C3.74, IgG1{kappa} isotypes) were raised against rat mannose-binding lectin (rMBL). Both mAbs recognized rMBL-A by Western analysis or surface plasmon resonance. P7E4, but not 14C3.74, exhibited a concentration-dependent inhibition of the lectin pathway, with maximal effect at 10 µg/mL. In vivo, rats were subjected to 30 minutes of left coronary artery occlusion and 4 hours of reperfusion. Complement C3 deposition was greatly attenuated in hearts pretreated with P7E4 compared with 14C3.74-treated hearts. Pretreatment with P7E4 (1 mg/kg) significantly reduced myocardial creatine kinase loss (48%), infarct size (39%), and neutrophil infiltration (47%) compared with 14C3.74-treated animals. In addition, P7E4 pretreatment significantly attenuated the expression of proinflammatory genes (intercellular adhesion molecule-1, vascular cell adhesion molecule-1, and interleukin-6) after ischemia-reperfusion.

Conclusions— The lectin complement pathway is activated after myocardial ischemia-reperfusion and leads to tissue injury. Blockade of the lectin pathway with inhibitory mAbs protects the heart from ischemia-reperfusion by reducing neutrophil infiltration and attenuating proinflammatory gene expression.


Key Words: ischemia • infarction • antibodies • cell adhesion molecules • inflammation




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