# IL-17A-producing NKp44(−) group 3 innate lymphoid cells accumulate in Familial Adenomatous Polyposis duodenal tissue

**Authors:** Kim M. Kaiser, Jan Raabe, Michael ToVinh, Gudrun Hack, Sarah Ahmad, Niko Müller, Julia Cassella, Sofia I. Walravens, Paula Alfaro, Lauren Arias Garcia, Dominik J. Kaczmarek, Tim Marwitz, Felix Goeser, Hans Dieter Nischalke, Philipp Lutz, Nils Sommer, Tim Vilz, Marieta Toma, Susanne Steiner, Oliver Hommerding, Johannes Oldenburg, Michael Hölzel, Sebastian Kadzik, Alexander Maas, Jonas Eckrich, Philipp Zumfelde, Farhad Shakeri, Svetozar Nesic, Andreas Buness, Emilia De Caro, Matthias Becker, Marc D. Beyer, Thomas Ulas, Anna C. Aschenbrenner, Lisa M. Steinheuer, Kevin Thurley, Sandy Kroh, Ralf Uecker, Anja E. Hauser, Florian N. Gohr, Florian I. Schmidt, Danni Wang, Kathrin Held, Olga Baranov, Christof Geldmacher, Christian P. Strassburg, Robert Hüneburg, Benjamin Krämer, Jacob Nattermann

PMC · DOI: 10.1038/s41467-025-58907-y · 2025-04-25

## TL;DR

This study shows that a specific type of immune cell accumulates in the duodenum of people with FAP and may contribute to tumor development.

## Contribution

The study identifies IL-17A-producing NKp44(−) group 3 innate lymphoid cells as a novel contributor to FAP-related tumorigenesis.

## Key findings

- IL-17A(+)NKp44(−)ILC3 cells are increased in FAP duodenal tissue and localized near the epithelium.
- IL-17A stimulation increases ROS production and DNA damage in FAP organoids, promoting tumorigenesis.
- Elevated IL1B, IL23A, and DLL4 transcripts correlate with IL-17A(+)NKp44(−)ILC3 accumulation in FAP.

## Abstract

Familial adenomatous polyposis (FAP) is an inherited gastrointestinal syndrome associated with duodenal adenoma formation. Even among carriers of the same genetic variant, duodenal phenotypes vary, indicating that additional factors, such as the local immune system, play a role. We observe an increase in duodenal IL-17A(+)NKp44(−) innate lymphoid type 3 cell (ILC3) in FAP, localized near the epithelium and enriched in adenomas and carcinomas. Elevated IL1B, IL23A, and DLL4 transcript levels correlate with IL-17A(+)NKp44(−)ILC3 accumulation, and in vitro studies with duodenal organoids confirmed this relationship. Bulk RNA sequencing reveals upregulated Reactive oxygen species (ROS)-inducing enzymes DUOX2 and DUOXA2 in FAP adenomas. IL-17A-stimulated FAP organoids show increased DUOX2/DUOXA2 expression, Duox2 protein, and ROS production, leading to DNA damage, suggesting a mechanism by which these immune cells promote tumorigenesis. These findings suggest IL-17A(+)NKp44(–)ILC3s may contribute to a local environment that makes the epithelium more submissive for oncogenic transformation in FAP.

Familial adenomatous polyposis (FAP) is an inherited gastrointestinal syndrome associated with duodenal adenoma formation. Here the authors show that IL17A-producing NKp44- group 3 innate lymphoid cells accumulate in FAP duodenal tissue and are associated with duodenal adenoma formation in patients with FAP.

## Linked entities

- **Genes:** IL1B (interleukin 1 beta) [NCBI Gene 3553], IL23A (interleukin 23 subunit alpha) [NCBI Gene 51561], DLL4 (delta like canonical Notch ligand 4) [NCBI Gene 54567], DUOX2 (dual oxidase 2) [NCBI Gene 50506], DUOXA2 (dual oxidase maturation factor 2) [NCBI Gene 405753]
- **Proteins:** IL17A (interleukin 17A), DUOX2 (dual oxidase 2)
- **Diseases:** Familial Adenomatous Polyposis (MONDO:0021055)

## Full-text entities

- **Genes:** DLL4 (delta like canonical Notch ligand 4) [NCBI Gene 54567] {aka AOS6, delta4, hdelta2}, DUOX2 (dual oxidase 2) [NCBI Gene 50506] {aka LNOX2, NOXEF2, P138-TOX, TDH6, THOX2}, NCR2 (natural cytotoxicity triggering receptor 2) [NCBI Gene 9436] {aka CD336, LY95, NK-p44, NKP44, dJ149M18.1}, DUOXA2 (dual oxidase maturation factor 2) [NCBI Gene 405753] {aka SIMNIPHOM, TDH5}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, IL23A (interleukin 23 subunit alpha) [NCBI Gene 51561] {aka IL-23, IL-23A, IL23P19, P19, SGRF}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}
- **Diseases:** inherited gastrointestinal syndrome (MESH:D009386), duodenal adenoma (MESH:D004382), FAP (MESH:D011125), tumorigenesis (MESH:D063646), adenomas and carcinomas (MESH:D000230)

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12032359/full.md

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Source: https://tomesphere.com/paper/PMC12032359