Human ectoenzyme-expressing ILC3: immunosuppressive innate cells that are depleted in graft-versus-host disease.

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is often associated with chemotherapy- and radiotherapy-induced host tissue damage, leading to graft-versus-host disease (GVHD). Innate lymphoid cells (ILC) have an essential role in tissue homeostasis and tissue repair via their production of interleukin (IL)-22, which acts on intestinal stem cells. The tissue healing capacities of ILC via IL-22 in the context of allo-HSCT and GVHD has previously been demonstrated in a mouse model for acute GVHD. We investigated potential other ways of ILC-mediated tissue protection against GVHD. Tissue injury leads to the release of danger-associated molecular patterns (DAMPs). DAMPs interact with purinergic receptors and ectoenzymes on immune cells and induce pleiotropic effects, including activation of proinflammatory antigen-presenting cells and immunosuppressive effects via the generation of adenosine. Here, we report a novel subset of human ILC3 that coexpress the ectoenzymes CD39 and CD73 (ecto+ ILC3). Ecto+ ILC3 express RORγt and were present in the oral-gastrointestinal tract and bone marrow. ILC3 ectoenzyme expression is modulated by the proinflammatory cytokine IL-1β. Extracellular adenosine triphosphate (eATP) stimulated ecto+ ILC3 to produce IL-22 and adenosine. Activated ecto+ ILC3 suppressed autologous T-cell proliferation in coculture experiments via the production of adenosine. In allo-HSCT recipients, intestinal GVHD was associated with reduced proportions of ecto+ ILC3 and decreased levels of adenosine and its metabolite inosine. Taken together, ecto+ ILC3 have immunosuppressive properties, but in patients with GVHD, ecto+ ILC3 are depleted. A lack of ecto+ ILC3 and subsequent reduced capacity to neutralize DAMPs may contribute to the development of GVHD.

[1]  G. Nilsson,et al.  Induction of human regulatory innate lymphoid cells from group 2 innate lymphoid cells by retinoic acid. , 2019, The Journal of allergy and clinical immunology.

[2]  J. Ritz,et al.  Functional analysis of clinical response to low-dose IL-2 in patients with refractory chronic graft-versus-host disease. , 2019, Blood advances.

[3]  R. Locksley,et al.  Innate Lymphoid Cells: 10 Years On , 2018, Cell.

[4]  J. Satsangi,et al.  Purine metabolism controls innate lymphoid cell function and protects against intestinal injury , 2018, Immunology and cell biology.

[5]  Yannick Simoni,et al.  Human Innate Lymphoid Cell Subsets Possess Tissue-Type Based Heterogeneity in Phenotype and Frequency. , 2018, Immunity.

[6]  Zhiheng Xu,et al.  Regulatory Innate Lymphoid Cells Control Innate Intestinal Inflammation , 2017, Cell.

[7]  J. Woosley,et al.  Type 2 innate lymphoid cells treat and prevent acute gastrointestinal graft-versus-host disease , 2017, The Journal of clinical investigation.

[8]  S. Robson,et al.  The ectonucleotidases CD39 and CD73: Novel checkpoint inhibitor targets , 2017, Immunological reviews.

[9]  N. McGovern,et al.  Human Innate Lymphoid Cell Subsets Possess Tissue‐Type Based Heterogeneity in Phenotype and Frequency , 2017, Immunity.

[10]  R. Negrin,et al.  Introduction to a review series on chronic GVHD: from pathogenic B-cell receptor signaling to novel therapeutic targets. , 2017, Blood.

[11]  F. Quintana,et al.  Regulation of the T Cell Response by CD39. , 2016, Trends in immunology.

[12]  M. Martelli,et al.  The NOTCH1/CD39 axis: a Treg trip-switch for GvHD , 2016, Leukemia.

[13]  M. Farrar,et al.  Group 3 innate lymphoid cells mediate intestinal selection of commensal bacteria–specific CD4+ T cells , 2015, Science.

[14]  G. Burnstock,et al.  Purinergic signalling and immune cells , 2014, Purinergic Signalling.

[15]  B. Blom,et al.  Activated innate lymphoid cells are associated with a reduced susceptibility to graft-versus-host disease. , 2014, Blood.

[16]  Liang Zhou,et al.  Group 3 innate lymphoid cells inhibit T-cell-mediated intestinal inflammation through aryl hydrocarbon receptor signaling and regulation of microflora. , 2013, Immunity.

[17]  E. Vizi,et al.  CD39 and CD73 in immunity and inflammation. , 2013, Trends in molecular medicine.

[18]  F. Bushman,et al.  Innate lymphoid cells regulate CD4+ T cell responses to intestinal commensal bacteria , 2013, Nature.

[19]  H. Tsukamoto,et al.  A delicate balance , 2013, Oncoimmunology.

[20]  R. Jenq,et al.  Interleukin-22 protects intestinal stem cells from immune-mediated tissue damage and regulates sensitivity to graft versus host disease. , 2012, Immunity.

[21]  F. Di Virgilio,et al.  Extracellular ATP Exerts Opposite Effects on Activated and Regulatory CD4+ T Cells via Purinergic P2 Receptor Activation , 2012, The Journal of Immunology.

[22]  M. Idzko,et al.  Deficiency of CD73/ecto-5'-nucleotidase in mice enhances acute graft-versus-host disease. , 2011, Blood.

[23]  S. Deaglio,et al.  Ectonucleotidases as regulators of purinergic signaling in thrombosis, inflammation, and immunity. , 2011, Advances in pharmacology.

[24]  M. Idzko,et al.  Graft-versus-host disease is enhanced by extracellular ATP activating P2X7R , 2010, Nature Medicine.

[25]  Courtney M. Lappas,et al.  Adenosine A2A receptor activation limits graft‐versus‐host disease after allogenic hematopoietic stem cell transplantation , 2010, Journal of leukocyte biology.

[26]  H. Friess,et al.  CD39 deletion exacerbates experimental murine colitis and human polymorphisms increase susceptibility to inflammatory bowel disease , 2009, Proceedings of the National Academy of Sciences.

[27]  A. la Sala,et al.  Hydrolysis of extracellular ATP and immune suppression: humans versus mice. , 2008, Blood.

[28]  Y. Wada,et al.  Rapid screening of high-risk patients for disorders of purine and pyrimidine metabolism using HPLC-electrospray tandem mass spectrometry of liquid urine or urine-soaked filter paper strips. , 2000, Clinical chemistry.

[29]  C. Szabó,et al.  Inosine Inhibits Inflammatory Cytokine Production by a Posttranscriptional Mechanism and Protects Against Endotoxin-Induced Shock1 , 2000, The Journal of Immunology.