Immunohistochemical Demonstration of Blood Group Antigen Expression in Intestinal Endothelium Links Blood Type and Necrotizing Enterocolitis

Charissa L Manuat, S. Yong, P. Dechristopher, C. Kwong, L. Glynn, O. Habeeb, Tricia L. Thomson, J. Muraskas
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引用次数: 6

Abstract

Objectives: To determine the presence of A and B blood group antigens on vascular endothelial cells of intestinal tissue and compare tissue resected for necrotizing enterocolitis (NEC) with tissues resected for non-NEC pathologies (spontaneous intestinal perforation (SIP), intussusception, Hirschsprung disease, intestinal atresia, etc.) in an effort to implicate blood group antigen expression on bowel endothelium as a mechanism of bowel injury in NEC via a humoral immune-mediated inflammatory response. Methods :Intestinal tissue from 21 patients with NEC and 23 non-NEC patients (5 of which were SIP) was stained with monoclonal antibodies against blood group antigens A and B. Vascular endothelial lined spaces were examined for expression of these blood group antigens and graded as 0 (no staining) to 3 (marked staining). Results: Control group birth gestational age (GA) ranged from 26 to 40 weeks (Mdn=36.4-37.0). Both NEC and SIP groups had birth GA ranging from 24 to 37 weeks (Mdn=29.3 and Mdn=27.6, respectively). Overall, A and B blood group antigens were appropriately expressed on the endothelium of all intestinal tissue regardless of the presence of NEC. The A antigen appeared to stain more intensely than the B antigen in most tissue, except for the NEC sample from an AB blood type patient in which A and B antigens stained equally intense (grade 3). Multivariate regression analysis confirms the significantly inverse relationship between gestational age and NEC, but a significant relationship could not be established between blood group or IHC scoring of the blood group antigen expression and NEC. 1.4 Conclusions: Blood group antigens, A more than B or AB together, may increase the risk of a neonate to develop NEC in the presence of passively or actively transferred isoagglutinins.
肠道内皮中血型抗原表达与坏死性小肠结肠炎关系的免疫组化研究
目的:测定肠组织血管内皮细胞上A和B血型抗原的存在,并将坏死性小肠结肠炎(NEC)切除的组织与非NEC病理(自发性肠穿孔(SIP)、肠套叠、巨结肠病、肠闭锁等)切除的组织进行比较,试图通过体液免疫介导的炎症反应,将肠内皮上的血型抗原表达作为NEC肠损伤的机制。方法:对21例NEC患者和23例非NEC患者(其中5例为SIP)的肠道组织进行抗血型抗原A和b的单克隆抗体染色,检测血管内皮细胞间隙中这两种血型抗原的表达,并按0(无染色)至3(有染色)分级。结果:对照组出生胎龄(GA) 26 ~ 40周(Mdn=36.4 ~ 37.0)。NEC组和SIP组新生儿GA均为24 ~ 37周(Mdn分别为29.3和27.6)。总体而言,无论是否存在NEC, A和B血型抗原都在所有肠组织的内皮上适当表达。在大多数组织中,A抗原比B抗原染色更强烈,除了AB血型患者的NEC样本中A抗原和B抗原染色同样强烈(3级)。多因素回归分析证实了胎龄与NEC之间存在显著的负相关关系,但血型或IHC评分的血型抗原表达与NEC之间没有显著的关系。1.4结论:在被动或主动转移的异凝集素存在的情况下,A多于B或AB的血型抗原可能增加新生儿发生NEC的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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