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Research Article Free access | 10.1172/JCI118195

Blockade of C5a and C5b-9 generation inhibits leukocyte and platelet activation during extracorporeal circulation.

C S Rinder, H M Rinder, B R Smith, J C Fitch, M J Smith, J B Tracey, L A Matis, S P Squinto, and S A Rollins

Department of Laboratory Medicine, Yale University School of Medicine, New Haven, Connecticut 06510, USA.

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Department of Laboratory Medicine, Yale University School of Medicine, New Haven, Connecticut 06510, USA.

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Department of Laboratory Medicine, Yale University School of Medicine, New Haven, Connecticut 06510, USA.

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Department of Laboratory Medicine, Yale University School of Medicine, New Haven, Connecticut 06510, USA.

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Department of Laboratory Medicine, Yale University School of Medicine, New Haven, Connecticut 06510, USA.

Find articles by Smith, M. in: PubMed | Google Scholar

Department of Laboratory Medicine, Yale University School of Medicine, New Haven, Connecticut 06510, USA.

Find articles by Tracey, J. in: PubMed | Google Scholar

Department of Laboratory Medicine, Yale University School of Medicine, New Haven, Connecticut 06510, USA.

Find articles by Matis, L. in: PubMed | Google Scholar

Department of Laboratory Medicine, Yale University School of Medicine, New Haven, Connecticut 06510, USA.

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Department of Laboratory Medicine, Yale University School of Medicine, New Haven, Connecticut 06510, USA.

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Published September 1, 1995 - More info

Published in Volume 96, Issue 3 on September 1, 1995
J Clin Invest. 1995;96(3):1564–1572. https://doi.org/10.1172/JCI118195.
© 1995 The American Society for Clinical Investigation
Published September 1, 1995 - Version history
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Abstract

Complement activation contributes to the systemic inflammatory response induced by cardiopulmonary bypass. At the cellular level, cardiopulmonary bypass activates leukocytes and platelets; however the contribution of early (3a) versus late (C5a, soluble C5b-9) complement components to this activation is unclear. We used a model of simulated extracorporeal circulation that activates complement (C3a, C5a, and C5b-9 formation), platelets (increased percentages of P-selectin-positive platelets and leukocyte-platelet conjugates), and neutrophils (upregulated CD11b expression). to specifically target complement activation in this model, we added a blocking mAb directed at the human C5 complement component and assessed its effect on complement and cellular activation. Compared with a control mAB, the anti-human C5 mAb profoundly inhibited C5a and soluble C5b-9 generation and serum complement hemolytic activity but had no effect on C3a generation. Additionally, the anti-human C5 mAb significantly inhibited neutrophil CD11b upregulation and abolished the increase in P-selectin-positive platelets and leukocyte-platelet conjugate formation compared to experiments performed with the control mAb. This suggests that the terminal components C5a and C5b-9, but not C3a, directly contribute to platelet and neutrophil activation during extracorporeal circulation. Furthermore, these data identify the C5 component as a site for therapeutic intervention in cardiopulmonary bypass.

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