Chimeric 7E3 Fab (ReoPro) decreases detectable CD11b on neutrophils from patients undergoing coronary angioplasty

Judith K. Mickelson, M. Nadir Ali, Neal S. Kleiman, Nasser M. Lakkis, Thomas W. Chow, Bonnie J. Hughes, C. Wayne Smith

Research output: Contribution to journalArticle

71 Scopus citations

Abstract

Objectives. The purpose of this study was to monitor the effects of chimeric 7E3 Fab (ReoPro) on leukocyte and platelet activation and interaction during coronary angioplasty. Background. Increased expression of CD11b on monocytes and neutrophils promotes their adhesion to endothelial cells, extracellular matrix and smooth muscle cells. Thrombin-activated platelets adhere via P-selectin to monocytes and neutrophils. These cell interactions may affect the outcome of coronary angioplasty. Methods. During coronary angioplasty, venous blood was obtained for flow cytometric detection of leukocyte CD11b; platelet CD41a, CD61a and CD62P; the percentage of leukocytes with adherent platelets and the intensity of hound platelet fluorescence. Results. Leukocyte CD11b expression increased after angioplasty in control patients (neutrophils 171 ± 25 to 255 ± 31 mean fluorescence intensity [MFI, mean ± SEM], n = 25, p < 0.0001; monocytes 200 ± 40 to 248 ± 36 MFI, n = 17, p < 0.05) and decreased in the patients selected to receive chimeric 7E3 Fab (neutrophils 146 ± 30 to 82 ± 22 MFI, n = 25, p < 0.0001; monocytes 256 ± 53 to 160 ± 38 MFI, n = 17, p < 0.05). Neutrophil CD11b decreased after in vitro incubation of whole blood with chimeric 7E3 Fab (n = 5, p = 0.01), but fMLP-induced increases in CD11b were not prevented. The CD11b expression was unchanged and increased with fMLP stimulation after in vitro incubation of isolated neutrophils with chimeric 7E3 Fab. Direct-labeled chimeric 7E3 Fab was not detected bound to neutrophils in whole blood or isolated cells using flow cytometric techniques. Adhesion of isolated neutrophils to protein-coated glass was not prevented by in vitro incubation with chimeric 7E3 Fab. Platelet activation increased after angioplasty in control patients (CD62P 8.9 ± 0.8 to 12.3 ± 1.2 MFI, n = 25, p < 0.05; CD41a 382 ± 25 to 454 ± 26 MFI, n = 25, p < 0.05, CD61a 436 ± 52 to 529 ± 58 MFI, n = 11, p < 0.05); it did not increase in the patients selected to receive chimeric 7E3 Fab (CD62P 13.2 ± 1.0 to 9.0 ± 0.9 MFI, n = 25, p < 0.05; CD61a 398 ± 32 to 410 ± 38 MFI, n = 7, p = NS). Leukocytes with adherent platelets tended to increase in the control group of patients and decrease after the procedure in patients selected to receive chimeric 7E3 Fab; individual and procedure-related variability were marked. Conclusions. Despite standard aspirin and heparin therapy, leukocyte and platelet activation with platelet adherence to leukocytes occurs after coronary angioplasty. Although chimeric 7E3 Fab does not bind to leukocytes directly, it influences CD11b expression in whole blood. Modulation of platelet and leukocyte activation and interaction by chimeric 7E3 Fab may contribute to an improved outcome after coronary angioplasty.

Original languageEnglish (US)
Pages (from-to)97-106
Number of pages10
JournalJournal of the American College of Cardiology
Volume33
Issue number1
DOIs
StatePublished - Jan 1999

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

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