Dual targeting of tumoral cells and immune microenvironment by blocking the IL-33/IL1RL1 pathway

Leukemia stem cells (LSCs) are a small yet powerful subset of leukemic cells that possess the ability to self-renew and have a long-term tumorigenic capacity, playing a crucial role in both leukemia development and therapy resistance. These LSCs are influenced by external and internal factors within the bone marrow niche. By delving into the intricate interplay between LSCs and their immune environment, we can pave the way for innovative immunotherapies that target both the malignant stem cells and the suppressive immune microenvironment, addressing both the "seed" and the "soil" simultaneously. Through the analysis of public datasets and patient samples, we show that elevated IL1RL1 expression correlates with poor prognosis and therapy resistance in acute myeloid leukemia (AML). At the core of this process, stem cell leukemogenesis initiation and maintenance signals are driven by a stress-induced IL-33/IL1RL1 autocrine loop. This LSC-induced IL-33/IL1RL1 signaling fosters an immune regulatory microenvironment. Therefore, IL1RL1 emerges as a promising therapeutic target, with IL1RL1-specific T cell-engaging bispecific antibodies holding great potential as cutting-edge immunotherapeutics for AML.

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Publication Details

Journal
Nature Communications
Published
2025-07-14
DOI
https://doi.org/10.1038/s41467-025-61567-7
Citations
5
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
3.99

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article

Dual targeting of tumoral cells and immune microenvironment by blocking the IL-33/IL1RL1 pathway

Alan Long, Maegan L. Capitano, Joshua R. Faust, Anilkumar Gopalakrishnapillai et al.
5 citations
Nature Communications
Immune Cell Function and Interaction
3.99
article

Dual targeting of tumoral cells and immune microenvironment by blocking the IL-33/IL1RL1 pathway

Alan Long, Maegan L. Capitano, Joshua R. Faust, Anilkumar Gopalakrishnapillai, Santhosh Kumar Pasupuleti, Nai‐Kong V. Cheung, Reuben Kapur, Sophie Paczesny, Baskar Ramdas, Hua Jiang, John Wrangle, Hong-Fen Guo, Denggang Fu, Sonali P. Barwe, Ella Harris
article en
5 citations

Abstract

Leukemia stem cells (LSCs) are a small yet powerful subset of leukemic cells that possess the ability to self-renew and have a long-term tumorigenic capacity, playing a crucial role in both leukemia development and therapy resistance. These LSCs are influenced by external and internal factors within the bone marrow niche. By delving into the intricate interplay between LSCs and their immune environment, we can pave the way for innovative immunotherapies that target both the malignant stem cells and the suppressive immune microenvironment, addressing both the "seed" and the "soil" simultaneously. Through the analysis of public datasets and patient samples, we show that elevated IL1RL1 expression correlates with poor prognosis and therapy resistance in acute myeloid leukemia (AML). At the core of this process, stem cell leukemogenesis initiation and maintenance signals are driven by a stress-induced IL-33/IL1RL1 autocrine loop. This LSC-induced IL-33/IL1RL1 signaling fosters an immune regulatory microenvironment. Therefore, IL1RL1 emerges as a promising therapeutic target, with IL1RL1-specific T cell-engaging bispecific antibodies holding great potential as cutting-edge immunotherapeutics for AML.

Nature CommunicationsVol. 16(1)
Memorial Sloan Kettering Cancer Center (US), Medical University of South Carolina (US), Center for Cancer and Blood Disorders (US), Indiana University School of Medicine, Indiana University – Purdue University Indianapolis (US)
U.S. Department of Defense, Fred Hutchinson Cancer Research Center, University of South Carolina, Hollings Cancer Center, Medical University of South Carolina, School of Medicine, Indiana University, Medical Research Council, National Cancer Institute, Moonshot Research and Development Program, Cancer Moonshot
Openalex Percentile: Top 6%
Immune Cell Function and Interaction
3.99
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