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高密度IgG4+浆细胞浸润与纤维狭窄型克罗恩病中的纤维增生相关。

High-Density IgG4+ Plasma Cells Infiltration Is Associated With Fibroplasia in Fibrostenotic Crohn's Disease.

作者信息

Escobar David, Bushara Omar, Sun Leyu, Liao Jie, Yang Guang-Yu

机构信息

Department of Pathology, Northwestern University, Feinberg School of Medicine, Chicago, IL, USA.

出版信息

Int J Surg Pathol. 2023 Sep;31(6):1085-1092. doi: 10.1177/10668969231152242. Epub 2023 Mar 3.

Abstract

Transmural fibrosis and stricture formation are key pathogenic processes for Crohn's disease that underlies clinical refractoriness, resulting in severe morbidity. The mechanisms for fibroplasia in Crohn's are not fully elucidated. In this study, we identified a cohort of refractory Crohn's disease with surgically resected bowel specimens including cases with bowel stricture and age-/sex-matched refractory disease without bowel stricture. Via immunohistochemistry, density and distribution of IgG4+ plasma cells in resected cases were analyzed. The histologic severity of fibrosis and association with gross evidence of stricture formation and IgG4+ plasma cells were comprehensively analyzed. Our results showed that density of IgG4+ plasma cells/high-power field (IgG4+ PCs/HPF) was significantly associated with increasing histologic fibrosis score (15 IgG4+ PCs/HPF in specimens with fibrosis score 0 vs 31 IgG4+ PC/HPF in fibrosis score 2 and 3,  = .039). Patients with gross evidence of stricture had significantly higher fibrosis scores compared to those without gross evidence of stricture ( = .044). There was a trend that mean IgG4+ plasma cell count was higher in Crohn's disease with gross stricture formation ( = .26), although it did not reach statistical significance (likely due to multiple pathogenesis events involved in bowel stricture formation besides IgG4+ plasma cells; such as transmural fibrosis, muscular hypertrophy, transmural ulcer/scar formation, and muscular-neural dysfunction). Our findings indicate IgG4+ plasma cells are associated with increasing histologic fibrosis in Crohn's. Further research is needed to establish a role for IgG4+ plasma cells in fibroplasia with an eye toward potential medical therapies targeting IgG4+ plasma cells to prevent transmural fibrosis.

摘要

透壁纤维化和狭窄形成是克罗恩病的关键致病过程,是临床难治性的基础,会导致严重的发病率。克罗恩病中纤维增生的机制尚未完全阐明。在本研究中,我们鉴定了一组经手术切除肠标本的难治性克罗恩病患者,包括有肠狭窄的病例以及年龄和性别匹配的无肠狭窄的难治性疾病病例。通过免疫组织化学分析切除病例中IgG4 +浆细胞的密度和分布。全面分析了纤维化的组织学严重程度以及与狭窄形成的大体证据和IgG4 +浆细胞的关联。我们的结果表明,IgG4 +浆细胞/高倍视野(IgG4 + PCs/HPF)的密度与组织学纤维化评分增加显著相关(纤维化评分为0的标本中为15个IgG4 + PCs/HPF,而纤维化评分为2和3的标本中为31个IgG4 + PC/HPF,P = 0.039)。有狭窄大体证据的患者与无狭窄大体证据的患者相比,纤维化评分显著更高(P = 0.044)。虽然未达到统计学意义(可能是由于除IgG4 +浆细胞外,肠狭窄形成还涉及多种致病事件;如透壁纤维化、肌肉肥大、透壁溃疡/瘢痕形成以及肌肉神经功能障碍),但在有明显狭窄形成的克罗恩病中,平均IgG4 +浆细胞计数有升高趋势(P = 0.26)。我们的研究结果表明,IgG4 +浆细胞与克罗恩病中组织学纤维化增加有关。需要进一步研究以确定IgG4 +浆细胞在纤维增生中的作用,着眼于针对IgG4 +浆细胞的潜在药物治疗以预防透壁纤维化。

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