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The single-cell transcriptional landscape of innate and adaptive lymphocytes in pediatric-onset colitis

Kokkinou, Efthymia (author)
Soini, Tea (author)
Karolinska Institutet
Pandey, Ram Vinay (author)
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van Acker, Aline (author)
Theorell, Jakob (author)
Karolinska Institutet
Czarnewski, Paulo, 1991- (author)
Stockholms universitet,Institutionen för biokemi och biofysik,Science for Life Laboratory (SciLifeLab)
Kvedaraite, Egle (author)
Karolinska Institutet
Vandamme, Niels (author)
Lourda, Magda (author)
Karolinska Institutet
Sorini, Chiara (author)
Karolinska Institutet
Weigel, Whitney (author)
Carrasco, Anna (author)
Karolinska Institutet
Tibbitt, Christopher Andrew (author)
Schlums, Heinrich (author)
Karolinska Institutet
Lindforss, Ulrik (author)
Karolinska Institutet
Nordenvall, Caroline (author)
Karolinska Institutet
Ljunggren, Malin (author)
Karolinska Institutet
Idestrom, Maja (author)
Svensson, Mattias (author)
Karolinska Institutet
Henter, Jan-Inge (author)
Karolinska Institutet
Villablanca, Eduardo J. (author)
Karolinska Institutet
Bryceson, Yenan T. (author)
Karolinska Institutet
Rolandsdotter, Helena (author)
Karolinska Institutet
Mjosberg, Jenny (author)
Karolinska Institutet
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 (creator_code:org_t)
2023
2023
English.
In: Cell reports medicine. - 2666-3791. ; 4:5
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Innate lymphoid cells (ILCs) are considered innate counterparts of adaptive T cells; however, their common and unique transcriptional signatures in pediatric inflammatory bowel disease (pIBD) are largely unknown. Here, we report a dysregulated colonic ILC composition in pIBD colitis that correlates with inflammatory ac-tivity, including accumulation of naive-like CD45RA+CD62L- ILCs. Weighted gene co-expression network analysis (WGCNA) reveals modules of genes that are shared or unique across innate and adaptive lympho-cytes. Shared modules include genes associated with activation/tissue residency, naivety/quiescence, and antigen presentation. Lastly, nearest-neighbor-based analysis facilitates the identification of most in-flamedand least inflamedlymphocytes in pIBD colon with unique transcriptional signatures. Our study reveals shared and unique transcriptional signatures of colonic ILCs and T cells in pIBD. We also provide insight into the transcriptional regulation of colonic inflammation, deepening our understanding of the poten-tial mechanisms involved in pIBD.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Immunologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Immunology in the medical area (hsv//eng)

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