Heterogeneity and clinical relevance of group 2 innate lymphoid cells subsets in nasal polyps
BACKGROUND: Chronic rhinosinusitis with nasal polyps is characterized by type 2 (T2) inflammation with elevated IL-5 and IL-13. Although group 2 innate lymphoid cells (ILC2s) drive T2 inflammation, their subset diversity and clinical relevance in nasal polyps (NPs) remain unclear. OBJECTIVE: We investigated cellular sources of T2 cytokines, subset heterogeneity of ILC2s, and the relationship between ILC2 subsets and clinical severity in chronic rhinosinusitis with NPs. METHODS: T cells were isolated from NP tissue and analyzed for cytokine production. ILC2s from 6 NP and 4 peripheral blood samples underwent single-cell RNA sequencing. Differential gene expression, subset heterogeneity, and pseudotime trajectory analyses were performed. Flow cytometry validated ILC2 subsets and associations with clinical parameters. RESULTS: 2 cells. NP-derived ILC2s showed downregulation of early developmental and trafficking genes (CD48, S1PR1) and upregulation of T2-associated cytokines (IL5, IL13), chemokines (XCL1, CXCL8), remodeling factors (AREG, TNFSF14), and METRNL. Four ILC2 subsets reflecting activation states were identified: migratory (tissue-homing with less activation), transitional (intermediate activation), inflammatory (high activation and T2 cytokines), and exhausted-like (expression of inhibitory receptors [eg, TIGIT]). The combined number of T2 cytokine-enriched subsets (transitional, inflammatory, and exhausted-like ILC2s) correlated with Lund-Mackay computed tomography scores. Inflammatory and exhausted-like ILC2s were associated with clinical symptom severity. CONCLUSION: ILC2s are one of the important effector populations driving local T2 inflammation in NPs and include 4 subsets with specific clinical associations. Subset-level ILC2 profiling may clarify chronic rhinosinusitis with NP pathophysiology and inform clinical stratification.
Authors
- Junqin Bai (ORCID: https://orcid.org/0000-0001-6012-2809)
- Mitsuhiro Okano (ORCID: https://orcid.org/0000-0002-4275-5781)
- Leslie C. Grammer (ORCID: https://orcid.org/0000-0001-6860-2014)
- Kevin C. Welch (ORCID: https://orcid.org/0000-0003-4863-7206)
- Robert C. Kern (ORCID: https://orcid.org/0000-0002-8995-9175)
- David B. Conley (ORCID: https://orcid.org/0000-0002-2611-6795)
- Aiko I. Klingler
- Naruhito Iwasaki (ORCID: https://orcid.org/0000-0001-5086-223X)
- Aiko Oka (ORCID: https://orcid.org/0000-0002-3648-2879)
- Julie A. Poposki
- Stephanie S. Smith (ORCID: https://orcid.org/0000-0002-0605-3993)
- W. David Stevens
- Micah Johnson (ORCID: https://orcid.org/0000-0001-6625-2719)
- Masanori Kidoguchi (ORCID: https://orcid.org/0000-0002-2599-4780)
- B. J. Y. Tan
- Noriko Ogasawara (ORCID: https://orcid.org/0000-0002-6014-3607)
- Lydia Suh
- Amr Radwan
- Anju T. Peters
- Atsushi Kato
- Aditi Agrwal
- Robert P. Schleimer
- Shigeharu Fujieda
Institutions
- University of Fukui (JP)
- Northwestern University (US)
- Regeneron (United States) (US)
- International University of Health and Welfare (JP)
Publication Details
- Journal
- Journal of Allergy and Clinical Immunology
- Published
- 2026-04-01
- DOI
- https://doi.org/10.1016/j.jaci.2026.03.021
- Primary Topic
- IL-33, ST2, and ILC Pathways
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Sanofi
- Uehara Memorial Foundation
- Japan Agency for Medical Research and Development
- Regeneron Pharmaceuticals
- Mochida Memorial Foundation for Medical and Pharmaceutical Research
- Japan Society for the Promotion of Science
- National Institute of Allergy and Infectious Diseases