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贫血伴恶性贫血和自身免疫性胃炎患者血清 IL-19 水平升高。

Elevated IL-19 Serum Levels in Patients With Pernicious Anemia and Autoimmune Gastritis.

机构信息

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.

Laboratory of Clinical Pathology, ULSS7 Pedemontana, Hospital Alto Vicentino, Santorso, Italy.

出版信息

Front Immunol. 2022 Apr 11;13:887256. doi: 10.3389/fimmu.2022.887256. eCollection 2022.

Abstract

Pernicious anemia (PA) is a megaloblastic anemia consisting of hematological, gastric and immunological alterations. The immunopathogenesis of PA is sustained by both autoantibodies (e.g. intrinsic factor (IFA) antibodies and anti parietal cell (PCA) antibodies and autoreactive T cells specific for IFA and the parietal cell proton pump ATPase. Iron deficient anemia (IDA) is a microcytic anemia and represents the most common cause of anemia worldwide. Our work aimed to investigate serum levels of several interleukins (IL) of the IL-20 cytokine subfamily in patients with PA, with IDA and in healthy subjects (HC). We compared serum levels of IL-19, IL-20, IL-26, IL-28A and IL-29 in 43 patients with PA and autoimmune gastritis, in 20 patients with IDA and no autoimmune gastritis, and in 47 HC. Furthermore, we analyzed the IL-19 cytokine production by gastric lamina propria mononuclear cells (LPMC) in eight patients with PA and four HC. We found that patients with PA have significantly higher serum levels of IL-19 (163.68 ± 75.96 pg/ml) than patients with IDA (35.49 ± 40.97 pg/ml; p<0.001) and healthy subjects (55.68 ± 36.75 pg/ml; p<0.001). Gastric LPMC from all PA patients were able to produce significantly higher levels of IL-19 (420.67 ± 68.14 pg/ml) than HC (53.69 ± 10.92 pg/ml) (<0.01). Altogether, our results indicate that IL-19 serum levels are significantly increased in patients with PA but not with IDA and that IL-19 is produced in the stomach of PA patients. These data open a new perspective on PA pathogenesis and suggest that IL-19 may represent a novel important tool for the management of patients with PA.

摘要

恶性贫血(PA)是一种巨幼细胞性贫血,包括血液学、胃和免疫学改变。PA 的免疫发病机制由自身抗体(例如内因子(IFA)抗体和壁细胞抗体(PCA)抗体以及针对 IFA 和壁细胞质子泵 ATP 酶的自身反应性 T 细胞维持。缺铁性贫血(IDA)是一种小细胞性贫血,是全世界最常见的贫血原因。我们的工作旨在研究 PA、IDA 和健康对照(HC)患者血清中几种白细胞介素(IL)-20 细胞因子亚家族的水平。我们比较了 43 例 PA 和自身免疫性胃炎、20 例 IDA 且无自身免疫性胃炎和 47 例 HC 患者的血清 IL-19、IL-20、IL-26、IL-28A 和 IL-29 水平。此外,我们分析了 8 例 PA 和 4 例 HC 患者胃固有层单核细胞(LPMC)的 IL-19 细胞因子产生。我们发现,PA 患者的血清 IL-19 水平明显高于 IDA 患者(163.68±75.96pg/ml 比 35.49±40.97pg/ml;p<0.001)和 HC(55.68±36.75pg/ml;p<0.001)。所有 PA 患者的胃 LPMC 产生的 IL-19 水平明显高于 HC(420.67±68.14pg/ml 比 53.69±10.92pg/ml;p<0.01)。总之,我们的结果表明,PA 患者的血清 IL-19 水平显著升高,但 IDA 患者则没有,并且 IL-19 在 PA 患者的胃中产生。这些数据为 PA 发病机制开辟了新的视角,并表明 IL-19 可能是 PA 患者管理的新的重要工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2d1/9036483/e2f48b5b7dbb/fimmu-13-887256-g001.jpg

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