Kaufman S S, Lyden E R, Marks W H, Lieberman J, Sudan D L, Fox I F, Shaw B W, Horslen S P, Langnas A N
Department of Pediatrics, University of Nebraska Medical Center, Omaha, USA.
Transplantation. 2001 Apr 27;71(8):1058-60. doi: 10.1097/00007890-200104270-00008.
The enterocyte-specific protein, intestinal fatty acid binding protein (I-FABP), is detectable in serum only after intestinal injury. Previous studies in animals suggest that I-FABP might be a useful marker of intestinal allograft rejection.
I-FABP was repetitively measured in nine intestinal transplant recipients and correlated with findings of surveillance endoscopy.
Average interval between I-FABP determination and biopsy was 3.4 days (SD=4.2 days). Average number of rejection episodes per patient totalled 1.6+/-1.2. General linear modeling demonstrated no tendency for increases in serum FABP to precede histologic graft rejection (P=0.263). Restriction of the analysis to I-FABP determinations 1 day before or on the day of biopsy failed to affect these results. Minor increases in I-FABP were often associated with histologically normal grafts, whereas rejection often occurred when I-FABP was not detectable.
Serum I-FABP levels do not predict clinical intestinal allograft rejection.
肠细胞特异性蛋白,即肠脂肪酸结合蛋白(I-FABP),仅在肠道损伤后才能在血清中检测到。先前在动物身上进行的研究表明,I-FABP可能是肠道同种异体移植排斥反应的有用标志物。
对9名肠道移植受者重复测量I-FABP,并将其与监测性内镜检查结果相关联。
I-FABP测定与活检之间的平均间隔为3.4天(标准差=4.2天)。每位患者的排斥反应发作平均次数总计为1.6±1.2次。一般线性模型显示血清FABP升高并无先于组织学移植排斥反应的趋势(P=0.263)。将分析限制在活检前1天或活检当天的I-FABP测定,并未影响这些结果。I-FABP的轻微升高通常与组织学上正常的移植物相关,而当I-FABP检测不到时,排斥反应往往会发生。
血清I-FABP水平无法预测临床肠道同种异体移植排斥反应。