TY - JOUR
T1 - Leukemia-driven expansion of type 3 innate lymphoid cell facilitates a pro-tumoral microenvironment in acute myeloid leukemia
AU - Dinh, Thanh Thanh T.
AU - Lordo, Matthew R.
AU - Zhang, Amy Y.
AU - Goda, Chinmayee
AU - Shilo, Nikolas
AU - Altynova, Ekaterina
AU - Ruesch, Michael
AU - Kronen, Parker
AU - Broughton, Megan
AU - Jeremy, Erin
AU - Sellers, Victoria L.
AU - Zhang, Xiaoli
AU - Larkin, Karilyn T.
AU - Collins, Patrick L.
AU - Dorrance, Adrienne M.
AU - Freud, Aharon G.
AU - Oakes, Christopher C.
AU - Mundy- Bosse, Bethany L.
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2026/2
Y1 - 2026/2
N2 - Acute myeloid leukemia (AML) is an aggressive hematologic malignancy with poor overall survival. Understanding how dysregulated immunity contributes to the development and progression of AML is an active area of investigation. Prior work has demonstrated functional defects in natural killer (NK) cells; however, the role of non-NK innate lymphoid cells (ILCs) in AML is incompletely understood. Conventional ILC3s are non-cytotoxic and regulate mucosal immunity through cytokine secretion. In this study, we discovered an expansion of ILC3s in both a murine model of AML and in AML patients. The transcription factor, aryl hydrocarbon receptor (AHR) is required for ILC3 development and function, and AML blasts have been shown to secrete AHR ligands. Modeling studies demonstrated ILC3 expansion was mediated by AHR activation in ILC precursors. ILC3s developed in leukemic settings had increased cytokine production, and co-culture of ILC3s significantly increased AML colony formation, which was mediated by ILC3-derived TNFα and GM-CSF. Furthermore, co-transfer of ILC3s with AML led to more rapid disease progression in vivo and human ILC3 frequency was associated with adverse risk stratification in AML patients. These data support a model in which AML promotes ILC3 expansion and function via an AHR-dependent mechanism to aid AML growth and survival.
AB - Acute myeloid leukemia (AML) is an aggressive hematologic malignancy with poor overall survival. Understanding how dysregulated immunity contributes to the development and progression of AML is an active area of investigation. Prior work has demonstrated functional defects in natural killer (NK) cells; however, the role of non-NK innate lymphoid cells (ILCs) in AML is incompletely understood. Conventional ILC3s are non-cytotoxic and regulate mucosal immunity through cytokine secretion. In this study, we discovered an expansion of ILC3s in both a murine model of AML and in AML patients. The transcription factor, aryl hydrocarbon receptor (AHR) is required for ILC3 development and function, and AML blasts have been shown to secrete AHR ligands. Modeling studies demonstrated ILC3 expansion was mediated by AHR activation in ILC precursors. ILC3s developed in leukemic settings had increased cytokine production, and co-culture of ILC3s significantly increased AML colony formation, which was mediated by ILC3-derived TNFα and GM-CSF. Furthermore, co-transfer of ILC3s with AML led to more rapid disease progression in vivo and human ILC3 frequency was associated with adverse risk stratification in AML patients. These data support a model in which AML promotes ILC3 expansion and function via an AHR-dependent mechanism to aid AML growth and survival.
UR - https://www.scopus.com/pages/publications/105025470976
U2 - 10.1038/s41375-025-02829-7
DO - 10.1038/s41375-025-02829-7
M3 - Article
C2 - 41430399
AN - SCOPUS:105025470976
SN - 0887-6924
VL - 40
SP - 325
EP - 338
JO - Leukemia
JF - Leukemia
IS - 2
ER -