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白细胞介素-37 参与传染性单核细胞增多症的免疫发病机制。

Interleukin-37 is involved in the immunopathogenesis of infectious mononucleosis.

机构信息

Institute of Immunology and Molecular Medicine, Jining Medical University, Jining, China.

Center for Laboratory Diagnosis, Yantai Yuhuangding Hospital Affiliated to Qingdao University, Yantai, China.

出版信息

Ital J Pediatr. 2023 Jul 28;49(1):93. doi: 10.1186/s13052-023-01498-5.

DOI:10.1186/s13052-023-01498-5
PMID:37507743
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10386628/
Abstract

BACKGROUND

Multiple immunopathological responses to viruses are observed in infectious mononucleosis (IM), a manifestation of primary infection with Epstein-Barr virus (EBV). Protective effects of the negative immunoregulatory molecule interleukin-37 (IL-37) have been observed in various bacterial and viral infections. However, the function of IL-37 in IM remains unknown.

METHODS

Flow cytometry and enzyme-linked immunosorbent assay (ELISA) were used to determine the expression of IL-37 in the peripheral blood of patients diagnosed with IM, and the variation of lymphocyte subsets. Furthermore, the associations between IL-37 expression and the percentage of lymphocyte subgroups were analyzed.

RESULTS

Patients with IM had severe immune dysfunction. The control group had a lower expression of IL-37 than the patients with IM. There were significant associations between IL-37 expression and both the proportion of CD3T cells and the ratio of CD3CD4 to CD3CD8T cells. Patients with higher levels of IL-37 expression had lower levels of the liver inflammation indicators, alanine aminotransferase (ALT) and aspartate aminotransferase (AST).

CONCLUSIONS

IL-37 may affect the immune pathogenesis of patients with IM infected with EBV, and may have immunotherapeutic benefit for EBV-associated illnesses.

摘要

背景

传染性单核细胞增多症(IM)是 EBV 原发感染的一种表现,患者体内存在针对多种病毒的免疫病理反应。负性免疫调节分子白细胞介素-37(IL-37)在多种细菌和病毒感染中具有保护作用,但 IL-37 在 IM 中的作用尚不清楚。

方法

采用流式细胞术和酶联免疫吸附试验(ELISA)检测诊断为 IM 的患者外周血中 IL-37 的表达及淋巴细胞亚群的变化,并分析 IL-37 表达与淋巴细胞亚群百分比之间的相关性。

结果

IM 患者存在严重的免疫功能障碍,IL-37 的表达水平低于对照组。IL-37 表达与 CD3T 细胞比例和 CD3CD4/CD3CD8T 细胞比值均呈显著正相关。IL-37 表达水平较高的患者,其肝炎症指标丙氨酸氨基转移酶(ALT)和天门冬氨酸氨基转移酶(AST)水平较低。

结论

IL-37 可能影响 EBV 感染所致 IM 患者的免疫发病机制,对 EBV 相关疾病可能具有免疫治疗作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffca/10386628/2f9fc5721181/13052_2023_1498_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffca/10386628/1093e93e6e9d/13052_2023_1498_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffca/10386628/279aa7ffb9c7/13052_2023_1498_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffca/10386628/dac703c972a5/13052_2023_1498_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffca/10386628/9799fb311e49/13052_2023_1498_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffca/10386628/12ec43b26adf/13052_2023_1498_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffca/10386628/2f9fc5721181/13052_2023_1498_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffca/10386628/1093e93e6e9d/13052_2023_1498_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffca/10386628/279aa7ffb9c7/13052_2023_1498_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffca/10386628/dac703c972a5/13052_2023_1498_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffca/10386628/9799fb311e49/13052_2023_1498_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffca/10386628/12ec43b26adf/13052_2023_1498_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffca/10386628/2f9fc5721181/13052_2023_1498_Fig6_HTML.jpg

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Novel Therapeutics for Epstein⁻Barr Virus.新型治疗 Epstein⁻Barr 病毒的方法。
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IL-37 isoform D downregulates pro-inflammatory cytokines expression in a Smad3-dependent manner.IL-37 同种型 D 通过 Smad3 依赖性途径下调促炎细胞因子的表达。
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