Settakorn Jongkolnee, Leong Anthony S Y
Division of Anatomical Pathology, Hunter Area Pathology Service, Newcastle, Australia.
Appl Immunohistochem Mol Morphol. 2004 Sep;12(3):198-204. doi: 10.1097/00129039-200409000-00003.
Subclinical or latent cases of gluten-sensitive enteropathy (GSE) are difficult to diagnose, and serology-positive, histology-negative (minimal morphologic change) and serology-negative, histology-positive patients have been identified. Both, particularly the histology-negative group, require the correct diagnosis for proper management, especially because the concept of minimal histologic change GSE has escaped attention in standard textbooks. We assessed the numbers and distribution of intraepithelial T cells and their subsets with CD3, CD8, and CD4 immunostaining and examined for crypt hyperplasia with mitotic and Ki-67 proliferative indices with the aim of refining the criteria for the diagnosis of minimal change GSE. Duodenal biopsies from 46 clinically suspected cases of GSE tested for antigliadin, antiendomysium, and antitissue transglutaminase antibodies were divided into four groups: serology-positive, histology-positive (S+H+, n = 20); serology-positive, histology-negative (S+H-, n = 22), representing the minimal morphologic change group; serology-negative, histology-positive (S-H+, n = 4); and serology-negative, histology-negative (S-H-, n = 28), controls with histologically normal duodenal biopsies obtained for unrelated reasons. The numbers of CD3+ and CD8+ intraepithelial T cells (IETCs) were significantly higher in histology-positive biopsies with (mean, 40.3/100 and 39.3/100 enterocytes, respectively) and without positive serology (mean, 33.3/100 and 35/100 enterocytes, respectively) compared with all other groups (S+H-, mean, 26.5/100 and 24.3/100 enterocytes, respectively; S-H-, mean, 23.3/100 and 17.9/100 enterocytes, respectively). Values for Ki-67 index in crypt enterocytes were also significantly different between histology-positive and histology-negative groups (P = 0.000). The distribution of CD3+ and CD8+ IETCs was mostly even along the surface enterocytes in histology-positive cases compared with the controls, which showed an uneven distribution. The 2 parameters that significantly discriminated between minimal morphologic change GSE (S+H-) and controls (S-H-) were Ki-67 index (P = 0.007) and the distribution pattern of CD8+ IETCs (P = 0.049). CD4 IETC counts were generally low, with no significant difference between all groups. The few S-H+ cases seen most likely represented false-negative serology, because the assessed parameters of this group and S+H+ cases were indistinguishable.
麸质敏感性肠病(GSE)的亚临床或潜伏病例难以诊断,已发现血清学阳性、组织学阴性(最小形态学改变)以及血清学阴性、组织学阳性的患者。这两类患者,尤其是组织学阴性组,需要正确诊断以进行恰当管理,特别是因为最小组织学改变GSE的概念在标准教科书中未得到关注。我们通过CD3、CD8和CD4免疫染色评估上皮内T细胞及其亚群的数量和分布,并通过有丝分裂和Ki-67增殖指数检查隐窝增生,目的是完善最小改变GSE的诊断标准。对46例临床疑似GSE病例的十二指肠活检组织进行抗麦醇溶蛋白、抗肌内膜和抗组织转谷氨酰胺酶抗体检测,并分为四组:血清学阳性、组织学阳性(S+H+,n = 20);血清学阳性、组织学阴性(S+H-,n = 22),代表最小形态学改变组;血清学阴性、组织学阳性(S-H+,n = 4);血清学阴性、组织学阴性(S-H-,n = 28),为因无关原因获取的组织学正常十二指肠活检组织作为对照。与所有其他组相比,组织学阳性活检组织(无论血清学是否阳性)中CD3+和CD8+上皮内T细胞(IETC)数量显著更高(有血清学阳性时,平均分别为40.3/100和39.3/100个肠上皮细胞;无血清学阳性时,平均分别为33.3/100和35/100个肠上皮细胞)(S+H-组,平均分别为26.5/100和24.3/100个肠上皮细胞;S-H-组,平均分别为23.3/100和17.9/100个肠上皮细胞)。隐窝肠上皮细胞中Ki-67指数在组织学阳性和组织学阴性组之间也有显著差异(P = 0.000)。与对照组相比,组织学阳性病例中CD3+和CD8+ IETC沿表面肠上皮细胞的分布大多均匀,而对照组显示分布不均匀。能显著区分最小形态学改变GSE(S+H-)和对照组(S-H-)的两个参数是Ki-67指数(P = 0.007)和CD8+ IETC的分布模式(P = 0.049)。CD4 IETC计数通常较低,所有组之间无显著差异。少数S-H+病例很可能代表血清学假阴性,因为该组和S+H+病例评估的参数无法区分。