Neutrophil expression of CD11b/CD18 and IL-8 secretion during normothermic cardiopulmonary bypass

J Cardiothorac Vasc Anesth. 1997 Aug;11(5):575-9. doi: 10.1016/s1053-0770(97)90007-0.

Abstract

Objective: To assess blood polymorphonuclear neutrophil (PMN) activation status during normothermic cardiopulmonary bypass (CPB), the expression of the PMN adhesion molecule CD11b/CD18 was measured. Basal state as well as ex vivo capacity of PMN to be stimulated by a bacterial peptide (FMLP) were investigated. Because interleukin-8 (IL-8) is known to induce CD11b/CD18 expression in vitro in PMN, IL-8 plasma levels were concomitantly measured.

Design: Prospective study.

Setting: University hospital.

Participants: Thirteen patients scheduled for cardiac surgery.

Interventions: Systemic arterial and pulmonary arterial blood samples were withdrawn at the same moment during the first 4 hours after the onset of CPB.

Measurements and main results: Twenty minutes after the onset of CPB, basal expression of PMN CD11b/CD18 was upregulated, whereas IL-8 plasma levels remained unchanged. The increase in PMN CD11b expression was maintained until the fourth hour after the onset of CPB. At this time, elevation of IL-8 plasma levels was maximal. No differences were found between pulmonary and systemic arterial IL-8 plasma levels, even after aortic unclamping. The capacity of PMN to be stimulated ex vivo by FMLP remained normal.

Conclusions: Normothermic CPB induced a fast increase in CD11b expression, which appeared to be similar to that observed during hypothermia. IL-8 was probably not related to the very early CD11b upregulation, but could be involved in pulmonary PMN sequestration during pulmonary reperfusion and contribute to the maintained expression of PMN CD11b. Although partially activated, PMNs maintain a normal capacity to respond to a further FMLP stimulation and thus to bacterial infection.

MeSH terms

  • Adult
  • Aged
  • CD18 Antigens / blood*
  • Cardiopulmonary Bypass*
  • Humans
  • Interleukin-8 / metabolism*
  • Macrophage-1 Antigen / blood*
  • Middle Aged
  • Neutrophils / metabolism*
  • Prospective Studies

Substances

  • CD18 Antigens
  • Interleukin-8
  • Macrophage-1 Antigen