Innate lymphoid cells in kidney diseases

被引:12
作者
Wang, Ruifeng [1 ]
Wang, Yiping [1 ]
Harris, David C. H. [1 ]
Cao, Qi [1 ]
机构
[1] Univ Sydney, Westmead Inst Med Res, Ctr Transplant & Renal Res, 176 Hawkesbury Rd, Sydney, NSW, Australia
基金
英国医学研究理事会;
关键词
innate immunity; innate lymphoid cells; kidney disease; therapy; IMMUNE-RESPONSES; IL-33; PROMOTES; VITAMIN-D; T-CELL; TYPE-2; INFLAMMATION; PLASTICITY; HOMEOSTASIS; IL-1-BETA; INFECTION;
D O I
10.1016/j.kint.2020.11.023
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
It is well known that innate immune cells, including dendritic cells, macrophages, and natural killer cells, contribute to pathogenesis and protection in various kidney diseases. The understanding of innate immunity has been advanced recently by the discovery of a new group of innate lymphoid cells (ILCs), including ILC1, ILC2, and ILC3. ILCs lack adaptive antigen receptors, yet can be triggered by various pathogens and rapidly provide an abundant source of immunomodulatory cytokines to exert immediate immune reactions and direct subsequent innate and adaptive immune responses. ILCs play critical roles in immunity, tissue homeostasis, and pathological inflammation. In this review, we highlight the biological function of ILC subpopulations in the normal kidney, and their important roles in acute and chronic kidney diseases, thus demonstrating the emerging importance of ILC-regulated immunity in this special organ and providing insights for future research directions and therapeutic interventions.
引用
收藏
页码:1077 / 1087
页数:11
相关论文
共 124 条
[91]   Group 1 innate lymphoid cells are involved in the progression of experimental anti-glomerular basement membrane glomerulonephritis and are regulated by peroxisome proliferator-activated receptor α [J].
Okabayashi, Yusuke ;
Nagasaka, Shinya ;
Kanzaki, Go ;
Tsuboi, Nobuo ;
Yokoo, Takashi ;
Shimizu, Akira .
KIDNEY INTERNATIONAL, 2019, 96 (04) :942-956
[92]   Systemically dispersed innate IL-13-expressing cells in type 2 immunity [J].
Price, April E. ;
Liang, Hong-Erh ;
Sullivan, Brandon M. ;
Reinhardt, R. Lee ;
Eisley, Chris J. ;
Erle, David J. ;
Locksley, Richard M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (25) :11489-11494
[93]   The T cell as a bridge between innate and adaptive immune systems: Implications for the kidney [J].
Rabb, H .
KIDNEY INTERNATIONAL, 2002, 61 (06) :1935-1946
[94]   IL-33-Dependent Group 2 Innate Lymphoid Cells Promote Cutaneous Wound Healing [J].
Rak, Gregory D. ;
Osborne, Lisa C. ;
Siracusa, Mark C. ;
Kim, Brian S. ;
Wang, Kelvin ;
Bayat, Ardeshir ;
Artis, David ;
Volk, Susan W. .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2016, 136 (02) :487-496
[95]   Resolution of inflammation by interleukin-9-producing type 2 innate lymphoid cells [J].
Rauber, Simon ;
Luber, Markus ;
Weber, Stefanie ;
Maul, Lisa ;
Soare, Alina ;
Wohlfahrt, Thomas ;
Lin, Neng-Yu ;
Dietel, Katharina ;
Bozec, Aline ;
Herrmann, Martin ;
Kaplan, Mark H. ;
Weigmann, Benno ;
Zaiss, Mario M. ;
Fearon, Ursula ;
Veale, Douglas J. ;
Canete, Juan D. ;
Distler, Oliver ;
Rivellese, Felice ;
Pitzalis, Costantino ;
Neurath, Markus F. ;
McKenzie, Andrew N. J. ;
Wirtz, Stefan ;
Schett, Georg ;
Distler, Joerg H. W. ;
Ramming, Andreas .
NATURE MEDICINE, 2017, 23 (08) :938-+
[96]   IL-33-Mediated Expansion of Type 2 Innate Lymphoid Cells Protects from Progressive Glomerulosclerosis [J].
Riedel, Jan-Hendrik ;
Becker, Martina ;
Kopp, Kerstin ;
Duester, Mathis ;
Brix, Silke R. ;
Meyer-Schwesinger, Catherine ;
Kluth, Luis A. ;
Gnirck, Ann-Christin ;
Attar, Madena ;
Krohn, Sonja ;
Fehse, Boris ;
Stahl, Rolf A. K. ;
Panzer, Ulf ;
Turner, Jan-Eric .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2017, 28 (07) :2068-2080
[97]   Type 2 innate lymphoid cell suppression by regulatory T cells attenuates airway hyperreactivity and requires inducible T-cell costimulator-inducible T-cell costimulator ligand interaction [J].
Rigas, Diamanda ;
Lewis, Gavin ;
Aron, Jennifer L. ;
Wang, Bowen ;
Banie, Homayon ;
Sankaranarayanan, Ishwarya ;
Galle-Treger, Lauriane ;
Maazi, Hadi ;
Lo, Richard ;
Freeman, Gordon J. ;
Sharpe, Arlene H. ;
Soroosh, Pejman ;
Akbari, Omid .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2017, 139 (05) :1468-+
[98]   Transcriptional programs define molecular characteristics of innate lymphoid cell classes and subsets [J].
Robinette, Michelle L. ;
Fuchs, Anja ;
Cortez, Victor S. ;
Lee, Jacob S. ;
Wang, Yaming ;
Durum, Scott K. ;
Gilfillan, Susan ;
Colonna, Marco .
NATURE IMMUNOLOGY, 2015, 16 (03) :306-U142
[99]   Cutaneous immunosurveillance and regulation of inflammation by group 2 innate lymphoid cells [J].
Roediger, Ben ;
Kyle, Ryan ;
Yip, Kwok Ho ;
Sumaria, Nital ;
Guy, Thomas V. ;
Kim, Brian S. ;
Mitchell, Andrew J. ;
Tay, Szun S. ;
Jain, Rohit ;
Forbes-Blom, Elizabeth ;
Chen, Xi ;
Tong, Philip L. ;
Bolton, Holly A. ;
Artis, David ;
Paul, William E. ;
Fazekas de St Groth, Barbara ;
Grimbaldeston, Michele A. ;
Le Gros, Graham ;
Weninger, Wolfgang .
NATURE IMMUNOLOGY, 2013, 14 (06) :564-+
[100]   Reduction of circulating innate lymphoid cell progenitors results in impaired cytokine production by innate lymphoid cells in patients with lupus nephritis [J].
Ryu, Seungwon ;
Lee, Eun Young ;
Kim, Dong Ki ;
Kim, Yon Su ;
Chung, Doo Hyun ;
Kim, Ji Hyung ;
Lee, Hajeong ;
Kim, Hye Young .
ARTHRITIS RESEARCH & THERAPY, 2020, 22 (01)