Expression of CD97 and adhesion molecules on circulating leukocytes in patients undergoing coronary artery bypass

B Gasz1, L Lenard, L Benko

  • 1Department of Surgical Research and Techniques, University of Pecs, Pecs, Hungary. balazs.gasz@aok.pte.hu

Insights

Cardiopulmonary bypass (CPB) significantly activates leukocytes, indicated by CD97 expression, especially in lymphocytes. Off-pump surgery shows less leukocyte activation, highlighting CD97

Area of Science:

  • Immunology
  • Cardiovascular Surgery
  • Biomarker Research

Background:

  • Leukocyte activation contributes to adverse effects after cardiopulmonary bypass (CPB).
  • CD97 is a novel cell surface molecule indicating leukocyte and lymphocyte activation.
  • Adhesion molecules CD11 and CD18 are also markers of leukocyte activation.

Purpose of the Study:

  • To compare CD97 and adhesion molecule expression on leukocyte subsets in patients undergoing coronary surgery with or without CPB.
  • To assess the role of CD97 as a marker for CPB-related inflammatory responses.

Main Methods:

  • Study included 30 patients: 20 with CPB (Group A) and 10 with off-pump (OP) surgery (Group B).
  • Blood samples were collected pre-surgery, during surgery, and up to 7 days post-surgery.
  • Expression of CD97, CD11, and CD18 on granulocytes, monocytes, and lymphocytes was analyzed.

Main Results:

  • CPB surgery led to decreased CD97 expression on granulocytes and monocytes, followed by a significant increase peaking on postoperative days 2-3.
  • CD97-positive lymphocytes gradually increased post-CPB, remaining elevated for 7 days.
  • OP surgery showed only moderate changes in CD97 expression across leukocyte subsets.
  • Adhesion molecule expression mirrored CD97 expression patterns.

Conclusions:

  • Coronary bypass with CPB induces substantial leukocyte activation compared to OP surgery.
  • Lymphocytes are highly activated and involved in leukocyte sequestration post-CPB.
  • CD97 is a significant indicator of the inflammatory response associated with CPB.
Abstract

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