Effects of IL-22 on cardiovascular diseases

被引:17
作者
Che, Yang [1 ,2 ]
Su, Zhaoliang [2 ,3 ]
Xia, Lin [1 ,2 ]
机构
[1] Jiangsu Univ, Dept Lab Med, Affiliated Hosp, 438 Jiefang Rd, Zhenjiang 212001, Jiangsu, Peoples R China
[2] Jiangsu Univ, Int Genome Ctr, Zhenjiang 212013, Jiangsu, Peoples R China
[3] Jiangsu Univ, Dept Immunol, Zhenjiang 212013, Jiangsu, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
IL-22; Cardiovascular diseases; Th22; cells; receptor; II CYTOKINE RECEPTOR; INTERLEUKIN; 22; IL-10; FAMILY; T-CELL; BLOOD-PRESSURE; HEART-FAILURE; MYOCARDITIS; EXPRESSION; DIFFERENTIATION; CLONING;
D O I
10.1016/j.intimp.2020.106277
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interleukin-22 (IL-22), which belongs to the IL-10 family, is an alpha helix cytokine specifically produced by many lymphocytes, such as Th1, Th17, Th22, ILCs, CD4 + and CD8 + T cells. In recent years, more and more studies have demonstrated that IL-22 has an interesting relationship with various cardiovascular diseases, including myocarditis, myocardial infarction, atherosclerosis, and other cardiovascular diseases, and IL-22 signal may play a dual role in cardiovascular diseases. Here, we summarize the recent progress on the source, function, regulation of IL-22 and the effects of IL-22 signal in cardiovascular diseases. The study of IL-22 will suggest more specific strategies to maneuver these functions for the effective treatment of cardiovascular diseases and future clinical treatment.
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页数:7
相关论文
共 96 条
[1]   Surface phenotype and antigenic specificity of human interleukin 17-producing T helper memory cells [J].
Acosta-Rodriguez, Eva V. ;
Rivino, Laura ;
Geginat, Jens ;
Jarrossay, David ;
Gattorno, Marco ;
Lanzavecchia, Antonio ;
Sallusto, Federica ;
Napolitani, Giorgio .
NATURE IMMUNOLOGY, 2007, 8 (06) :639-646
[2]   Atorvastatin, losartan and captopril may upregulate IL-22 in hypertension and coronary artery disease; the role of gene polymorphism [J].
Akbari, Hamed ;
Asadikaram, Gholamreza ;
Jafari, Ahmad ;
Nazari-Robati, Mahdieh ;
Ebrahimi, Ghasem ;
Ebrahimi, Nazanin ;
Masoumi, Mohammad .
LIFE SCIENCES, 2018, 207 :525-531
[3]  
[Anonymous], CIRCULATION
[4]   Urinary interleukin 22 binding protein as a marker of lupus nephritis in Egyptian children with juvenile systemic lupus erythematosus [J].
Badr, Ahmed Mohamed Mahmoud ;
Farag, Yomna ;
Abdelshafy, Maie ;
Riad, Nermine Magdi .
CLINICAL RHEUMATOLOGY, 2018, 37 (02) :451-458
[5]   Th22 Cells Are an Important Source of IL-22 for Host Protection against Enteropathogenic Bacteria [J].
Basu, Rajatava ;
O'Quinn, Darrell B. ;
Silberger, Daniel J. ;
Schoeb, Trenton R. ;
Fouser, Lynette ;
Ouyang, Wenjun ;
Hatton, Robin D. ;
Weaver, Casey T. .
IMMUNITY, 2012, 37 (06) :1061-1075
[6]   Vascular Smooth Muscle Cells in Atherosclerosis [J].
Bennett, Martin R. ;
Sinha, Sanjay ;
Owens, Gary K. .
CIRCULATION RESEARCH, 2016, 118 (04) :692-702
[7]   IL-22 inhibits epidermal differentiation and induces proinflammatory gene expression and migration of human keratinocytes [J].
Boniface, K ;
Bernard, FX ;
Garcia, M ;
Gurney, AL ;
Lecron, JC ;
Morel, F .
JOURNAL OF IMMUNOLOGY, 2005, 174 (06) :3695-3702
[8]   Presenting Systolic Blood Pressure and Outcomes in Patients With Acute Aortic Dissection [J].
Bossone, Eduardo ;
Gorla, Riccardo ;
LaBounty, Troy M. ;
Suzuki, Toru ;
Gilon, Dan ;
Strauss, Craig ;
Ballotta, Andrea ;
Patel, Himanshu J. ;
Evangelista, Arturo ;
Ehrlich, Marek P. ;
Hutchison, Stuart ;
Kline-Rogers, Eva ;
Montgomery, Daniel G. ;
Nienaber, Christoph A. ;
Isselbacher, Eric M. ;
Eagle, Kim A. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2018, 71 (13) :1432-1440
[9]   IL-22 is increased in active Crohn's disease and promotes proinflammatory gene expression and intestinal epithelial cell migration [J].
Brand, S ;
Beigel, F ;
Olszak, T ;
Zitzmann, K ;
Eichhorst, ST ;
Otte, JM ;
Diepolder, H ;
Marquardt, A ;
Jagla, W ;
Popp, A ;
Leclair, S ;
Herrmann, K ;
Seiderer, J ;
Ochsenkühn, T ;
Göke, B ;
Auernhammer, CJ ;
Dambacher, J .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2006, 290 (04) :G827-G838
[10]   23, 22 Calling the Microbiota to Control Atherosclerosis [J].
Carreras, Alba ;
Backhed, Fredrik .
IMMUNITY, 2018, 49 (05) :788-790