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Ann Thorac Surg 1992;53:611-616
© 1992 The Society of Thoracic Surgeons


Articles

Effect of cardiopulmonary bypass on circulating lymphocyte function

Dao M. Nguyen, MD1, David S. Mulder, MD, Hani Shennib, MD*,2

Montreal Lung Transplant Program and The Montreal General Hospital, Montreal, Quebec, Canada

Received for publication September 6, 1991. * Address reprint requests to Dr Shennib, The Montreal General Hospital, 1650 Cedar Ave, Room 9827 L.H., Montreal, Que, Canada H3G 1A4.

Extracorporeal cardiopulmonary bypass (CPB) has been associated with a wide variety of immunalogical derangements, including a transient postoperative impairment of lymphocyte function. We examined changes in phenotypic and nonspecific cytotoxicity of peripheral blood mononuclear cells after extracorporeal CPB. The peripheral blood samples obtained from 10 patients were subjected to natural killer and cytotoxic T lymphocyte activity assay before and at intervals after CPB. Phenotypic] analysis of peripheral blood lymphocytes was performed in 5 patients before and immediately after CPB. We observed a significant increase in peripheral blood CD8+ cells (cytotoxic/suppressor T lymphocytes) (16.1% ± 2.5% versus 22.5% ± 2.1%; p < .005) and a decrease in CD4+ cells (helper/inducer T lymphocytes) (46.1% ± 3.5% versus 36.1% ± 3.5%;p < 0.02) immediately after extracorporeal circulation. The CD8/CD4 ratio in peripheral blood was significantly increased immediately after bypass (0.53 versus 0.80; p < 9.001). No significant changes in percentages of other leukocyte subsets in peripheral blood were noted. The activity of cytotoxic T lymphocytes and natural killer cells in peripheral blood was impaired on postoperative days 1 and 3 but was restored to preoperative values by removal of mononuclear phagocytes from these cells. The decrease in natural killer cell and cytotoxic T lymphocyte activity in peripheral blood may signify a temporary impairment of the effector arm of the cell-mediated immunity in the post-operative period. The observed changes in peripheral blood phenotype and function may be involved in early organ injury and infectious complications after CPB.




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