Mickelson J K, Ali M N, Kleiman N S, Lakkis N M, Chow T W, Hughes B J, Smith C W
Department of Medicine, Baylor College of Medicine, Veterans Administration Medical Center, Houston, Texas 77030, USA.
J Am Coll Cardiol. 1999 Jan;33(1):97-106. doi: 10.1016/s0735-1097(98)00532-4.
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.
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.
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 bound platelet fluorescence.
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.
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.
本研究旨在监测嵌合型7E3 Fab(ReoPro)在冠状动脉成形术期间对白细胞和血小板激活及相互作用的影响。
单核细胞和中性粒细胞上CD11b表达增加会促进它们与内皮细胞、细胞外基质和平滑肌细胞的黏附。凝血酶激活的血小板通过P-选择素与单核细胞和中性粒细胞黏附。这些细胞间相互作用可能会影响冠状动脉成形术的结果。
在冠状动脉成形术期间,采集静脉血用于流式细胞术检测白细胞CD11b;血小板CD41a、CD61a和CD62P;黏附血小板的白细胞百分比以及结合血小板的荧光强度。
在对照患者中,冠状动脉成形术后白细胞CD11b表达增加(中性粒细胞平均荧光强度[MFI,平均值±标准误]从171±25增至255±31,n = 25,p < 0.0001;单核细胞从200±40增至248±36 MFI,n = 17,p < 0.05),而在选择接受嵌合型7E3 Fab的患者中则降低(中性粒细胞从146±30降至82±22 MFI,n = 25,p < 0.0001;单核细胞从256±53降至160±38 MFI,n = 17,p < 0.05)。全血与嵌合型7E3 Fab体外孵育后,中性粒细胞CD11b降低(n = 5,p = 0.01),但fMLP诱导的CD11b增加未被阻止。分离的中性粒细胞与嵌合型7E3 Fab体外孵育后,CD11b表达未改变,且在fMLP刺激下增加。使用流式细胞术技术未检测到直接标记的嵌合型7E3 Fab与全血或分离细胞中的中性粒细胞结合。体外与嵌合型7E3 Fab孵育未阻止分离的中性粒细胞与蛋白包被玻璃的黏附。对照患者冠状动脉成形术后血小板激活增加(CD62P从8.9±0.8增至12.3±1.2 MFI,n = 25,p < 0.05;CD41a从382±25增至454±26 MFI,n = 25,p < 0.05,CD61a从436±52增至529±58 MFI,n = 11,p < 0.05);在选择接受嵌合型7E3 Fab的患者中未增加(CD62P从13.2±1.0降至9.0±0.9 MFI,n = 25,p < 0.05;CD61a从398±32增至410±38 MFI,n = 7,p = 无显著性差异)。黏附血小板的白细胞在对照组患者中趋于增加,而在选择接受嵌合型7E3 Fab的患者术后则减少;个体差异和与手术相关的变异性很明显。
尽管采用了标准的阿司匹林和肝素治疗,冠状动脉成形术后仍会发生白细胞和血小板激活以及血小板与白细胞的黏附。虽然嵌合型7E3 Fab不直接与白细胞结合,但它会影响全血中CD11b的表达。嵌合型7E3 Fab对血小板和白细胞激活及相互作用的调节可能有助于改善冠状动脉成形术后的结果。