A unique intestinal epithelial cell that expresses canonical lymphoid genes

Enterocytes and intestinal secretory cells harbor innate immunity. However, certain transcriptional programs –even beyond rearranged T- and B-cell receptor genes– are considered the exclusive purview of adaptive immune cells, including abundant and diverse intestinal intra-epithelial lymphocytes (IELs). Here, we identify and characterize columnar intestinal secretory cells that co-express classic epithelial and lymphoid genes, including Ptprc , Cd3e , Cd8a , and Gzma/b but not T- or B-cell receptors. These previously unrecognized epithelium-derived lymphoid-like cells (EDLCs) differ from any known resident cell type, including IELs or tuft cells. Rare in healthy mouse and human intestines, their numbers increase upon IL-25 stimulation or IL-10 receptor deficiency in vivo and upon IL-13 stimulation in vitro . EDLC chromatin is uniquely accessible at thousands of cis -elements, including lymphoid and epithelial loci. These findings reveal a transcriptionally and epigenetically distinct intestinal epithelial derivative that expresses prominent lymphoid character.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-10-26
DOI
https://doi.org/10.64898/2026.10.21.760658
Primary Topic
IL-33, ST2, and ILC Pathways
Type
preprint

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preprint

A unique intestinal epithelial cell that expresses canonical lymphoid genes

Krithika Badarinath, Ruiyang He, Semir Beyaz, James R. Goldenring et al.
bioRxiv (Cold Spring Harbor Laboratory)
IL-33, ST2, and ILC Pathways
preprint

A unique intestinal epithelial cell that expresses canonical lymphoid genes

Krithika Badarinath, Ruiyang He, Semir Beyaz, James R. Goldenring, Bin Bao, Scott B. Snapper, Ramesh A. Shivdasani, Su‐Hyung Lee, Guodong Tie, Swarnabh Bhattacharya, Onur Eskiocak, Pratik N.P. Singh, Kun Huang
preprint en

Abstract

Enterocytes and intestinal secretory cells harbor innate immunity. However, certain transcriptional programs –even beyond rearranged T- and B-cell receptor genes– are considered the exclusive purview of adaptive immune cells, including abundant and diverse intestinal intra-epithelial lymphocytes (IELs). Here, we identify and characterize columnar intestinal secretory cells that co-express classic epithelial and lymphoid genes, including Ptprc , Cd3e , Cd8a , and Gzma/b but not T- or B-cell receptors. These previously unrecognized epithelium-derived lymphoid-like cells (EDLCs) differ from any known resident cell type, including IELs or tuft cells. Rare in healthy mouse and human intestines, their numbers increase upon IL-25 stimulation or IL-10 receptor deficiency in vivo and upon IL-13 stimulation in vitro . EDLC chromatin is uniquely accessible at thousands of cis -elements, including lymphoid and epithelial loci. These findings reveal a transcriptionally and epigenetically distinct intestinal epithelial derivative that expresses prominent lymphoid character.

bioRxiv (Cold Spring Harbor Laboratory)
Boston Children's Hospital (US), Cold Spring Harbor Laboratory (US), Dana-Farber Cancer Institute (US), Vanderbilt University Medical Center (US)
U.S. Department of Veterans Affairs, National Institutes of Health
IL-33, ST2, and ILC Pathways
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