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活化诱导胞苷脱氨酶在伴有 IgG4 阳性细胞的眼附属器边缘区淋巴瘤中的上调表达。

Upregulated Expression of Activation-Induced Cytidine Deaminase in Ocular Adnexal Marginal Zone Lymphoma with IgG4-Positive Cells.

机构信息

Division of Pathophysiology, Okayama University Graduate School of Health Sciences, Okayama 700-8558, Japan.

Department of General Medicine, Okayama University Hospital, Okayama 700-8558, Japan.

出版信息

Int J Mol Sci. 2021 Apr 15;22(8):4083. doi: 10.3390/ijms22084083.

Abstract

Immunoglobulin G4-related disease (IgG4-RD) is a systemic disorder characterized by tissue fibrosis and intense lymphoplasmacytic infiltration, causing progressive organ dysfunction. Activation-induced cytidine deaminase (AID), a deaminase normally expressed in activated B-cells in germinal centers, edits ribonucleotides to induce somatic hypermutation and class switching of immunoglobulin. While AID expression is strictly controlled under physiological conditions, chronic inflammation has been noted to induce its upregulation to propel oncogenesis. We examined AID expression in IgG4-related ophthalmic disease (IgG4-ROD; = 16), marginal zone lymphoma with IgG4-positive cells (IgG4+ MZL; = 11), and marginal zone lymphoma without IgG4-positive cells (IgG4- MZL; = 12) of ocular adnexa using immunohistochemical staining. Immunohistochemistry revealed significantly higher AID-intensity index in IgG4-ROD and IgG4+ MZL than IgG4- MZL ( < 0.001 and = 0.001, respectively). The present results suggest that IgG4-RD has several specific causes of AID up-regulation in addition to inflammation, and AID may be a driver of oncogenesis in IgG4-ROD to IgG4+ MZL.

摘要

免疫球蛋白 G4 相关疾病(IgG4-RD)是一种以组织纤维化和大量淋巴浆细胞浸润为特征的系统性疾病,导致进行性器官功能障碍。激活诱导胞嘧啶脱氨酶(AID)是一种在生发中心活化 B 细胞中正常表达的脱氨酶,它编辑核苷酸以诱导免疫球蛋白的体细胞超突变和类别转换。虽然在生理条件下 AID 的表达受到严格控制,但慢性炎症已被证明可诱导其上调以促进肿瘤发生。我们使用免疫组织化学染色检查了 16 例 IgG4 相关眼病(IgG4-ROD)、11 例伴有 IgG4 阳性细胞的边缘区淋巴瘤(IgG4+ MZL)和 12 例无 IgG4 阳性细胞的边缘区淋巴瘤(IgG4- MZL)中的 AID 表达。免疫组化显示,IgG4-ROD 和 IgG4+ MZL 中的 AID 强度指数明显高于 IgG4- MZL(<0.001 和=0.001)。这些结果表明,除了炎症之外,IgG4-RD 还有几个导致 AID 上调的特定原因,并且 AID 可能是 IgG4-ROD 向 IgG4+ MZL 肿瘤发生的驱动因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1dd/8071226/5431afded264/ijms-22-04083-g001.jpg

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