IL13Rα2 expression identifies tissue‐resident IL‐22‐producing PLZF+ innate T cells in the human liver

Innate lymphocytes are selectively enriched in the liver where they have important roles in liver immunology. Murine studies have shown that type I NKT cells can promote liver inflammation, whereas type II NKT cells have an anti‐inflammatory role. In humans, type II NKT cells were found to accumulat...

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Bibliographic Details
Published in:European journal of immunology Vol. 48; no. 8; pp. 1329 - 1335
Main Authors: Paquin‐Proulx, Dominic, Greenspun, Benjamin C., Pasquet, Lise, Strunz, Benedikt, Aleman, Soo, Falconer, Karolin, Terabe, Masaki, Berzofsky, Jay A., Sandberg, Johan K., Melum, Espen, Nixon, Douglas F., Björkström, Niklas K.
Format: Journal Article
Language:English
Published: Germany Wiley Subscription Services, Inc 01.08.2018
Subjects:
Biomarkers - metabolism
Hepatocytes
Human liver
Humans
IL13Rα2
IL‐22
Immunologic Memory - immunology
Immunological memory
Inflammation
Innate T cells
Interleukin 1
Interleukin-13 Receptor alpha2 Subunit - metabolism
Interleukin-22
Interleukins - metabolism
Leukemia
Liver
Liver - cytology
Liver - immunology
Lymphocytes
Lymphocytes T
Memory cells
Natural killer cells
Natural Killer T-Cells - immunology
Phenotypes
PLZF
Promyelocytic Leukemia Zinc Finger Protein - metabolism
Sulfatide
T cell receptors
Zinc finger proteins
Innate T cells
IL13Rα2
IL-22
PLZF
Human liver
ISSN:0014-2980, 1521-4141, 1521-4141
Online Access:Get full text
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Summary:Innate lymphocytes are selectively enriched in the liver where they have important roles in liver immunology. Murine studies have shown that type I NKT cells can promote liver inflammation, whereas type II NKT cells have an anti‐inflammatory role. In humans, type II NKT cells were found to accumulate in the gut during inflammation and IL13Rα2 was proposed as a marker for these cells. In the human liver, less is known about type I and II NKT cells. Here, we studied the phenotype and function of human liver T cells expressing IL13Rα2. We found that IL13Rα2 was expressed by around 1% of liver‐resident memory T cells but not on circulating T cells. In support of their innate‐like T‐cell character, the IL13Rα2+ T cells had higher expression of promyelocytic leukaemia zinc finger (PLZF) compared to IL13Rα2− T cells and possessed the capacity to produce IL‐22. However, only a minority of human liver sulfatide‐reactive type II NKT cells expressed IL13Rα2. Collectively, these findings suggest that IL13Rα2 identifies tissue‐resident intrahepatic T cells with innate characteristics and the capacity to produce IL‐22. Innate lymphocytes are selectively enriched in the liver where they have important roles in liver immunology. We identified that human liver IL13Rα2+ T cells have tissue‐resident memory T cells with innate characteristics and the capacity to produce IL‐22, which may play a role in protection from fibrosis.
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ISSN:0014-2980
1521-4141
1521-4141
DOI:10.1002/eji.201747334