Innate Lymphoid Cells: Role in Immune Regulation and Cancer

被引:16
作者
Chung, Douglas C. [1 ,2 ]
Jacquelot, Nicolas [2 ]
Ghaedi, Maryam [2 ]
Warner, Kathrin [2 ]
Ohashi, Pamela S. [1 ,2 ]
机构
[1] Univ Toronto, Dept Immunol, Toronto, ON M5S 1A8, Canada
[2] Univ Hlth Network, Princess Margaret Canc Ctr, Toronto, ON M5G 2M9, Canada
关键词
immune regulation; cancer; innate lymphoid cells; natural killer cells; tumour microenvironment; ILCregs; T cells; Treg; adaptive immunity; immune suppression; ovarian carcinoma; NATURAL-KILLER-CELLS; EPITHELIAL OVARIAN-CANCER; CD4(+) T-CELLS; TUMOR-ASSOCIATED MACROPHAGES; HUMAN DENDRITIC CELLS; NK CELLS; POOR-PROGNOSIS; IN-VIVO; IMMUNOGLOBULIN-SYNTHESIS; DEPENDENT MECHANISM;
D O I
10.3390/cancers14092071
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Innate lymphoid cells (ILCs) are an emerging family of effector cells known to play a major role in innate defenses against pathogens, lymphoid organogenesis, tissue repair, and homeostasis. They are positioned strategically within tissues to provide the first line of defence and shape the ensuing adaptive immune cell response. Recent evidence suggests that ILCs contribute to immune regulation in different diseases, including cancer, and can have significant impact on disease outcome. In this review, we highlight the immunosuppressive roles of ILCs in cancer that inhibit effective immune surveillance and anti-tumour response. Immune regulation is composed of a complex network of cellular and molecular pathways that regulate the immune system and prevent tissue damage. It is increasingly clear that innate lymphoid cells (ILCs) are also armed with immunosuppressive capacities similar to well-known immune regulatory cells (i.e., regulatory T cells). In cancer, immunoregulatory ILCs have been shown to inhibit anti-tumour immune response through various mechanisms including: (a) direct suppression of anti-tumour T cells or NK cells, (b) inhibiting T-cell priming, and (c) promoting other immunoregulatory cells. To provide a framework of understanding the role of immunosuppressive ILCs in the context of cancer, we first outline a brief history and challenges related to defining immunosuppressive ILCs. Furthermore, we focus on the mechanisms of ILCs in suppressing anti-tumour immunity and consequentially promoting tumour progression.
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页数:22
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共 217 条
[111]   Multi-tissue single-cell analysis deconstructs the complex programs of mouse natural killer and type 1 innate lymphoid cells in tissues and circulation [J].
McFarland, Adelle P. ;
Yalin, Adam ;
Wang, Shuang-Yin ;
Cortez, Victor S. ;
Landsberger, Tomer ;
Sudan, Raki ;
Peng, Vincent ;
Miller, Hannah L. ;
Ricci, Biancamaria ;
David, Eyal ;
Faccio, Roberta ;
Amit, Ido ;
Colonna, Marco .
IMMUNITY, 2021, 54 (06) :1320-+
[112]   Low-dose IL-2 induces CD56bright NK regulation of T cells via NKp44 and NKp46 [J].
McQuaid, S. L. ;
Loughran, S. T. ;
Power, P. A. ;
Maguire, P. ;
Szczygiel, A. ;
Johnson, P. A. .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2020, 200 (03) :228-241
[113]  
Mehrotra PT, 1998, J IMMUNOL, V160, P2637
[114]   Cutting edge:: Human CD4+CD25+ T cells restrain the maturation and antigen-presenting function of dendritic cells [J].
Misra, N ;
Bayry, J ;
Lacroix-Desmazes, S ;
Kazatchkine, MD ;
Kaveri, SV .
JOURNAL OF IMMUNOLOGY, 2004, 172 (08) :4676-4680
[115]  
Molinero LL, 2002, J LEUKOCYTE BIOL, V71, P791
[116]   ILC2s amplify PD-1 blockade by activating tissue-specific cancer immunity [J].
Moral, John Alec ;
Leung, Joanne ;
Rojas, Luis A. ;
Ruan, Jennifer ;
Zhao, Julia ;
Sethna, Zachary ;
Ramnarain, Anita ;
Gasmi, Billel ;
Gururajan, Murali ;
Redmond, David ;
Askan, Gokce ;
Bhanot, Umesh ;
Elyada, Ela ;
Park, Youngkyu ;
Tuveson, David A. ;
Gonen, Mithat ;
Leach, Steven D. ;
Wolchok, Jedd D. ;
DeMatteo, Ronald P. ;
Merghoub, Taha ;
Balachandran, Vinod P. .
NATURE, 2020, 579 (7797) :130-+
[117]   Dendritic Cell Editing by Activated Natural Killer Cells Results in a More Protective Cancer-Specific Immune Response [J].
Morandi, Barbara ;
Mortara, Lorenzo ;
Chiossone, Laura ;
Accolla, Roberto S. ;
Mingari, Maria Cristina ;
Moretta, Lorenzo ;
Moretta, Alessandro ;
Ferlazzo, Guido .
PLOS ONE, 2012, 7 (06)
[118]   CD56brightCD16- NK Cells Produce Adenosine through a CD38-Mediated Pathway and Act as Regulatory Cells Inhibiting Autologous CD4+ T Cell Proliferation [J].
Morandi, Fabio ;
Horenstein, Alberto L. ;
Chillemi, Antonella ;
Quarona, Valeria ;
Chiesa, Sabrina ;
Imperatori, Andrea ;
Zanellato, Silvia ;
Mortara, Lorenzo ;
Gattorno, Marco ;
Pistoia, Vito ;
Malavasi, Fabio .
JOURNAL OF IMMUNOLOGY, 2015, 195 (03) :965-972
[119]   Soluble HLA-G dampens CD94/NKG2A expression and function and differentially modulates chemotaxis and cytokine and chemokine secretion in CD56bright and CD56dim NK cells [J].
Morandi, Fabio ;
Ferretti, Elisa ;
Castriconi, Roberta ;
Dondero, Alessandra ;
Petretto, Andrea ;
Bottino, Cristina ;
Pistoia, Vito .
BLOOD, 2011, 118 (22) :5840-5850
[120]  
MORIO T, 1989, CLIN EXP IMMUNOL, V78, P159