Thylén P, Lundahl J, Fernvik E, Hed J, Svenson S B, Jacobson S H
Department of Medicine, Karolinska Hospital, Stockholm, Sweden.
Am J Nephrol. 1992;12(6):393-400. doi: 10.1159/000168488.
We studied the upregulation of the intracellular glycoprotein Mac-1 (CD11b/CD18, CR3) on monocytes and granulocytes during 36 bicarbonate hemodialyses in 12 patients who were randomly treated with Cuprophan (Cu), Hemophan (He) or Polysulfone (PS; low-flux) membranes. The degree of mobilization of this adhesion protein was related to changes in granulocyte and monocyte count, generation of C3a and production of interleukin-1 beta in plasma. Mac-1 expression on granulocytes was significantly higher after 5 and 15 min of Cu hemodialysis as compared to He or PS dialyses (p < 0.001) and correlated to changes in granulocyte count at 15 min (r = 0.62 and r = 0.76, p < 0.001). No differences in early Mac-1 mobilization on circulating monocytes was observed despite a decrease in cell count. Mac-1 expression on monocytes and granulocytes in the venous blood line at 180 min of treatment was significantly higher during Cu dialysis as compared to He and PS dialyses (p < 0.02 and p < 0.001, respectively). Early generation of C3a was higher in patients on Cu dialysis than in He or PS dialysis (p < 0.001) and correlated both to granulocytopenia (r = 0.45, p < 0.01) and to the subsequent increase in Mac-1 expression on granulocytes (r = 0.63, p < 0.001). An early increase in Mac-1 expression on monocytes was accompanied by an increase in plasma interleukin-1 beta later during dialysis (p < 0.05). Studies of Mac-1 expression during hemodialysis increased the sensitivity of biocompatibility measurements and correlated better than complement generation to changes in granulocyte count as it mediates adhesion to endothelial cells.
我们研究了12例患者在36次碳酸氢盐血液透析过程中,单核细胞和粒细胞内糖蛋白Mac-1(CD11b/CD18,CR3)的上调情况。这些患者被随机采用铜仿膜(Cu)、血仿膜(He)或聚砜膜(PS;低通量)进行治疗。这种黏附蛋白的动员程度与粒细胞和单核细胞计数的变化、C3a的生成以及血浆中白细胞介素-1β的产生有关。与He或PS透析相比,Cu血液透析5分钟和15分钟后,粒细胞上Mac-1的表达显著更高(p<0.001),且与15分钟时粒细胞计数的变化相关(r=0.62和r=0.76,p<0.001)。尽管细胞计数有所下降,但未观察到循环单核细胞早期Mac-1动员的差异。与He和PS透析相比,治疗180分钟时静脉血路中单核细胞和粒细胞上Mac-1的表达在Cu透析期间显著更高(分别为p<0.02和p<0.001)。Cu透析患者中C3a的早期生成高于He或PS透析(p<0.001),且与粒细胞减少(r=0.45,p<0.01)以及随后粒细胞上Mac-1表达的增加相关(r=0.63,p<0.001)。单核细胞上Mac-1表达的早期增加伴随着透析后期血浆白细胞介素-1β的增加(p<0.05)。血液透析期间Mac-1表达的研究提高了生物相容性测量的敏感性,并且与补体生成相比,与粒细胞计数的变化相关性更好,因为它介导与内皮细胞的黏附。