Journal Article

No prominent role for terminal complement activation in the early myocardial reperfusion phase following cardiac surgery

Kirsten A. Kortekaas, Pieter van der Pol, Jan H.N. Lindeman, Carla C. Baan, Cees van Kooten and Robert J.M. Klautz

in European Journal of Cardio-Thoracic Surgery

Published on behalf of European Association for Cardio-Thoracic Surgery

Volume 41, issue 5, pages e117-e125
Published in print May 2012 | ISSN: 1010-7940
Published online March 2012 | e-ISSN: 1873-734X | DOI: https://dx.doi.org/10.1093/ejcts/ezs088
No prominent role for terminal complement activation in the early myocardial reperfusion phase following cardiac surgery

More Like This

Show all results sharing these subjects:

  • Cardiovascular Medicine
  • Cardiothoracic Surgery

GO

Show Summary Details

Preview

OBJECTIVES

Complement activation is considered an important mediator of myocardial ischaemia/reperfusion (I/R) injury. Although complement inhibitors are highly effective in animals, clinical trials fail to show a substantial benefit in humans. This raises questions on the role of complement activation in human myocardial I/R injury.

METHODS

Soluble C5b-9, i.e. terminal complement complex, and C5a were assessed in patients with non-ischaemic (n = 10) and ischaemic heart failure (n = 10), and patients without heart failure (n = 10) undergoing cardiac surgery. To study the pathophysiology of human I/R injury, a model of arteriovenous measurements over the reperfused heart was applied at consecutive time points during the early reperfusion phase. Furthermore, C3d and C5b-9 depositions in pre-reperfusion myocardial and endomyocardial tissue were evaluated and compared to pre-transplantation tissue from myocardial allografts.

RESULTS

Simultaneous assessment of soluble C5b-9 and C5a in systemical and myocardial venous blood samples revealed the absence of net release from the reperfused heart in all three patient groups. Biopsies of patients with non-ischaemic heart failure showed the most abundant myocardial depositions of C3d and C5b-9: 4.8 times more C3d (P = 0.008) and 4.7 times more C5b-9 (P = 0.004) than donor tissue. Also C3d was abundantly present in endomyocardial tissue of both heart failure groups compared to donors (both P = 0.02).

CONCLUSIONS

No evidence was obtained that terminal complement activation is involved in the acute phase following myocardial reperfusion. Since complement deposition was already present before reperfusion, human complement inhibition might be more beneficial in the preoperative phase than during reperfusion.

Keywords: Immunology; Inflammation; Ischaemia; Reperfusion; Surgery

Journal Article.  4737 words.  Illustrated.

Subjects: Cardiovascular Medicine ; Cardiothoracic Surgery

Full text: subscription required

How to subscribe Recommend to my Librarian

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content. subscribe or login to access all content.