TY - JOUR
T1 - Review
T2 - Innate Lymphoid Cells: Sparking Inflammatory Rheumatic Disease?
AU - Wenink, Mark H
AU - Leijten, Emmerik F A
AU - Cupedo, Tom
AU - Radstake, Timothy R D J
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2017/5
Y1 - 2017/5
N2 - Immunology research is in a constant state of flux with new cell types being described on a regular basis. While most rheumatologists are familiar with the role that “T cell cytokines” such as tumor necrosis factor (TNF), interferon-g (IFNg), and interleukin-17A (IL- 17A) play in the pathogenesis of rheumatic diseases, what many may not know is that an array of innate counterparts to the conventional T cells have recently been discovered that are capable of rapidly producing these same effector cytokines. These innate counterparts include g/d T cells, invariant natural killer (iNK) cells, mucosa-associated invariant T (MAIT) cells, and innate lymphoid cells (ILCs). An insightful overview of g/d T cells, iNK cells, and MAIT cells in rheumatic disease has recently been published (1); therefore, the current review focuses on ILCs. Strikingly, some of the ILCs have only recently been discovered, in part due to their relative scarcity in peripheral blood, and their presence in numerous organs of the human body has subsequently been described. In this review, we provide the newest insights into the potential role of ILCs in the field of rheumatology and provide recommendations for future ILC research that will help to promote our understanding of rheumatic diseases even further.
AB - Immunology research is in a constant state of flux with new cell types being described on a regular basis. While most rheumatologists are familiar with the role that “T cell cytokines” such as tumor necrosis factor (TNF), interferon-g (IFNg), and interleukin-17A (IL- 17A) play in the pathogenesis of rheumatic diseases, what many may not know is that an array of innate counterparts to the conventional T cells have recently been discovered that are capable of rapidly producing these same effector cytokines. These innate counterparts include g/d T cells, invariant natural killer (iNK) cells, mucosa-associated invariant T (MAIT) cells, and innate lymphoid cells (ILCs). An insightful overview of g/d T cells, iNK cells, and MAIT cells in rheumatic disease has recently been published (1); therefore, the current review focuses on ILCs. Strikingly, some of the ILCs have only recently been discovered, in part due to their relative scarcity in peripheral blood, and their presence in numerous organs of the human body has subsequently been described. In this review, we provide the newest insights into the potential role of ILCs in the field of rheumatology and provide recommendations for future ILC research that will help to promote our understanding of rheumatic diseases even further.
U2 - 10.1002/art.40068
DO - 10.1002/art.40068
M3 - Article
C2 - 28217945
SN - 2326-5191
VL - 69
SP - 885
EP - 897
JO - Arthritis & Rheumatology
JF - Arthritis & Rheumatology
IS - 5
ER -