Department of Clinical Immunology & Rheumatology, Christian Medical College, Vellore, Tamil Nadu, 632004, India.
Department of Pathology, Christian Medical College, Vellore, India.
Clin Rheumatol. 2024 Mar;43(3):1103-1110. doi: 10.1007/s10067-023-06861-9. Epub 2024 Feb 3.
Fibrosis is a typical pathological characteristic in IgG4-RD patients and often irreversible. There exists a lack of suitable markers for detection of earlier onset of fibrosis in various organs in IgG4-RD patients. Hence, this study aims at analysing ambispectively the myofibroblasts and the pro-fibrotic cytokines, IFN gamma and IL-33 involved in IgG4-RD associated fibrosis in South Asian patients.
Archived biopsy samples of definite/probable/possible cases of IgG4-RD, classified according to diagnostic criteria, taken from patients who attended the OPD and IPD of our tertiary care centre during January 2015-January 2020 were chosen for this study. The paraffin sections were examined qualitatively for fibrosis and the excessive collagen deposition by Hematoxylin & Eosin and Masson's Trichrome staining. Also, the presence of alpha-Smooth muscle actin (α-SMA) expressing myofibroblasts and the involvement of pro-fibrotic cytokines (IFN-gamma, IL-33) were assessed by Immunohistochemistry and scored semi-quantitatively (+mild, ++moderate, +++ severe). Serum IL-33 levels were analysed by indirect Elisa (R & D Systems).
Myofibroblasts were present in 10/12 biopsy samples, in moderate levels in 4 (33%) and very high levels (+++) in 3 (25%) of the patients. IFN-gamma was expressed at low levels in 6 (50%) and absent in 6 (50%). All patients showed IL-33 expression with very high levels in tissue (6, 50%), as well as in serum samples.
The findings of this study reinforce the role of myofibroblasts and profibrotic cytokines like IL-33 in fibrosis of Ig4-RD patients, pointing to their potential as earlier predictive markers of onset and extent of fibrosis.
纤维化是 IgG4-RD 患者的典型病理特征,且通常不可逆转。目前缺乏用于检测 IgG4-RD 患者各器官纤维化早期发病的合适标志物。因此,本研究旨在分析南亚患者 IgG4-RD 相关纤维化中涉及的肌成纤维细胞和促纤维化细胞因子 IFNγ和 IL-33。
选择 2015 年 1 月至 2020 年 1 月期间在我们的三级护理中心门诊和住院部就诊的 IgG4-RD 明确/可能/疑似病例的存档活检样本,根据诊断标准进行分类。通过苏木精和伊红及 Masson 三色染色对纤维化和过度胶原沉积进行定性检查。同时,通过免疫组织化学评估表达α-平滑肌肌动蛋白(α-SMA)的肌成纤维细胞的存在和促纤维化细胞因子(IFN-γ,IL-33)的参与,并进行半定量评分(+轻度,++中度,+++重度)。通过间接 ELISA(R&D Systems)分析血清 IL-33 水平。
在 12 个活检样本中,有 10 个样本存在肌成纤维细胞,其中 4 个(33%)中度存在,3 个(25%)高度存在。IFN-γ在 6 个(50%)样本中低表达,在 6 个(50%)样本中缺失。所有患者的组织(6,50%)和血清样本中均有 IL-33 高表达。
本研究结果进一步证实了肌成纤维细胞和促纤维化细胞因子如 IL-33 在 IgG4-RD 患者纤维化中的作用,提示它们可能成为纤维化发病和程度的早期预测标志物。