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本文引用的文献

1
A cytokine network involving IL-36γ, IL-23, and IL-22 promotes antimicrobial defense and recovery from intestinal barrier damage.涉及白细胞介素-36γ、白细胞介素-23 和白细胞介素-22 的细胞因子网络可促进抗菌防御并从肠道屏障损伤中恢复。
Proc Natl Acad Sci U S A. 2018 May 29;115(22):E5076-E5085. doi: 10.1073/pnas.1718902115. Epub 2018 May 14.
2
Endothelial STAT3 Modulates Protective Mechanisms in a Mouse Ischemia-Reperfusion Model of Acute Kidney Injury.内皮细胞 STAT3 调节急性肾损伤缺血再灌注模型中的保护机制。
J Immunol Res. 2017;2017:4609502. doi: 10.1155/2017/4609502. Epub 2017 Oct 17.
3
Evidence for Involvement of IL-9 and IL-22 in Cows' Milk Allergy in Infants.婴儿牛奶过敏中白细胞介素-9 和白细胞介素-22 的作用证据。
Nutrients. 2017 Sep 21;9(10):1048. doi: 10.3390/nu9101048.
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JAK2/STAT3 Pathway Was Associated with the Protective Effects of IL-22 On Aortic Dissection with Acute Lung Injury.JAK2/STAT3 通路与白细胞介素 22 对急性肺损伤性主动脉夹层的保护作用有关。
Dis Markers. 2017;2017:1917804. doi: 10.1155/2017/1917804. Epub 2017 Jul 30.
5
IL-22 modulates inflammatory properties of human primary aortic smooth muscle cells.白细胞介素-22调节人原代主动脉平滑肌细胞的炎症特性。
Adv Clin Exp Med. 2017 May-Jun;26(3):461-466. doi: 10.17219/acem/62218.
6
Regulation of T17 Cells and Associated Cytokines in Wound Healing, Tissue Regeneration, and Carcinogenesis.伤口愈合、组织再生和癌症发生过程中T17细胞及相关细胞因子的调控
Int J Mol Sci. 2017 May 11;18(5):1033. doi: 10.3390/ijms18051033.
7
Serum levels of interleukin-22, cardiometabolic risk factors and incident type 2 diabetes: KORA F4/FF4 study.白细胞介素-22血清水平、心血管代谢危险因素与2型糖尿病发病:KORA F4/FF4研究
Cardiovasc Diabetol. 2017 Jan 31;16(1):17. doi: 10.1186/s12933-017-0498-6.
8
Lacrimal gland-derived IL-22 regulates IL-17-mediated ocular mucosal inflammation.泪腺源性白介素-22 调节白介素-17 介导的眼黏膜炎症。
Mucosal Immunol. 2017 Sep;10(5):1202-1210. doi: 10.1038/mi.2016.119. Epub 2017 Jan 4.
9
Interleukin-22 Might Act as a Double-Edged Sword in Type 2 Diabetes and Coronary Artery Disease.白细胞介素-22在2型糖尿病和冠状动脉疾病中可能扮演双刃剑的角色。
Mediators Inflamm. 2016;2016:8254797. doi: 10.1155/2016/8254797. Epub 2016 Oct 18.
10
IL-22 is rapidly induced by Pathogen Recognition Receptors Stimulation in Bone-Marrow-derived Dendritic Cells in the Absence of IL-23.在缺乏白细胞介素-23的情况下,病原体识别受体刺激可迅速诱导骨髓来源的树突状细胞产生白细胞介素-22。
Sci Rep. 2016 Sep 22;6:33900. doi: 10.1038/srep33900.

白细胞介素-22,一种治疗非自身免疫性疾病的有效靶点。

Interleukin-22, a potent target for treatment of non-autoimmune diseases.

作者信息

Zheng Yue, Li Tong

机构信息

a Cardiology , The Third Central Clinical College of Tianjin Medical University , Tianjin , China.

b Cardiology , Tianjin Key Laboratory of Artificial Cell.

出版信息

Hum Vaccin Immunother. 2018;14(12):2811-2819. doi: 10.1080/21645515.2018.1509649. Epub 2018 Oct 31.

DOI:10.1080/21645515.2018.1509649
PMID:30335564
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6343613/
Abstract

Interleukin -22 (IL-22) is a member of interleukin-10 (IL-10) family cytokines that is produced by different types of lymphocytes included in both innate and adaptive immune systems. These lymphocytes include activated T cells, most notably Th17 and Th22 cells, as well as NK cells, γδ T cells, etc. IL-22 mediate its effects via the IL-22-IL-22R complex and subsequent Janus Kinase-signal transduces and activators transcription (JAK-STAT) signaling pathway. According to recent evidence, IL-22 played a critical role in the pathogenesis of many non-autoimmune diseases. In this review, we mainly discussed the recent findings and advancements of the role of IL-22 in several non-autoimmune diseases, such as acute lung injury, atherosclerosis and some bacterial infections, suggesting that IL-22 may have therapeutic potential for treating non-autoimmune diseases.

摘要

白细胞介素-22(IL-22)是白细胞介素-10(IL-10)家族细胞因子的成员,由先天免疫系统和适应性免疫系统中的不同类型淋巴细胞产生。这些淋巴细胞包括活化的T细胞,最显著的是Th17和Th22细胞,以及自然杀伤细胞、γδT细胞等。IL-22通过IL-22-IL-22R复合物以及随后的Janus激酶-信号转导和转录激活因子(JAK-STAT)信号通路介导其作用。根据最近的证据,IL-22在许多非自身免疫性疾病的发病机制中起关键作用。在本综述中,我们主要讨论了IL-22在几种非自身免疫性疾病(如急性肺损伤、动脉粥样硬化和一些细菌感染)中的作用的最新发现和进展,表明IL-22可能具有治疗非自身免疫性疾病的潜力。