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白细胞介素-35:控制糖尿病前期和慢性炎症性1型自身免疫性糖尿病的关键因子。

Interleukin-35: A key player managing pre-diabetes and chronic inflammatory type 1 autoimmune diabetes.

作者信息

Chakraborty Ratul, Mukherjee Ashis Kumar, Bala Asis

机构信息

Life Sciences Division, Institute of Advanced Study in Science and Technology, Guwahati 781035, Guwahati, Assam, India.

Pharmacology and Drug Discovery Research Laboratory, Division of Life Sciences, Institute of Advanced Study in Science and Technology, Guwahati 781035, Assam, India.

出版信息

World J Diabetes. 2024 Oct 15;15(10):2147-2151. doi: 10.4239/wjd.v15.i10.2147.

Abstract

Interleukin-35 (IL-35) is a novel protein comprising IL-12α and IL-27β chains. The IL12A and genes are responsible for its production. The study of IL-35 has experienced a substantial increase in interest in recent years, as demonstrated by many research papers. Recent clinical studies have shown that individuals who do not have a C-peptide have notably reduced amounts of IL-35 in their blood serum. This is accompanied by a drop in the percentage of IL-35 Treg cells, regulatory B cells, and CD8 FOXP3 cells that produce IL-35. This article em-phasizes the potential significance of IL-35 expression in governing the immune response and its involvement in chronic inflammatory autoimmune diabetes in pancreatic inflammation. It demonstrates IL-35's ability to regulate cytokine proportions, modulate B cells, and protect against autoimmune diabetes. However, further investigation is necessary to ascertain the precise mechanism of IL-35, and meticulous planning is essential for clinical studies.

摘要

白细胞介素-35(IL-35)是一种由IL-12α和IL-27β链组成的新型蛋白质。IL12A和相关基因负责其产生。近年来,对IL-35的研究兴趣大幅增加,许多研究论文都证明了这一点。最近的临床研究表明,没有C肽的个体血清中IL-35的含量显著降低。这伴随着产生IL-35的IL-35调节性T细胞、调节性B细胞和CD8 FOXP3细胞百分比的下降。本文强调了IL-35表达在控制免疫反应中的潜在意义及其在胰腺炎症中的慢性炎症性自身免疫性糖尿病中的作用。它证明了IL-35调节细胞因子比例、调节B细胞以及预防自身免疫性糖尿病的能力。然而,有必要进一步研究以确定IL-35的确切机制,并且精心规划对于临床研究至关重要。

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