Interleukin-10 Autoantibodies and HLA-DRB1*01:03 in Inflammatory Bowel Disease

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Authors: Nima Gharahdaghi, Pai‐Jui Yeh, Lourdes Ceron‐Gutierrez, H Griffin, Hannah Gordon, Chamara Jayamanne, Alice Fracchia, Amanda Y. Chong, Alissa Walsh, Oliver Brain, Katherine Baker, Hannah Kockelbergh
+38 more Yang Luo, Martha Guevara Becerra, Katherine Vadakethala, Madeleine Coy, Ladan Kabiri, Martin Barnardo, Susanna Dunachie, Barbara Kronsteiner, Anna Adams, Darren Fowler, Qian Zhang, Laura Fachal, Carl A. Anderson, R Desoki, Marie Vibeke Vestergaard, Lone Larsen, Nicola J Wyatt, Robert Lees, Robert J. Mulligan, Chaonan Dong, Mohmmed Tauseef Sharip, S Faustini, Adrian Shields, Julia Pakpoor, Bushra Naz, Alex Richter, Jack Satsangi, Christopher A. Lamb, M Parkes, Fiona Powrie, Alexander J. Mentzer, Aleksejs Sazonovs, Tine Jess, P Klenerman, Simon Travis, Sophie Hambleton, Rainer Döffinger, Holm H. Uhlig
Cited by: 10
References: 35

Abstract

BACKGROUND: Neutralizing autoantibodies against interleukin-10 can result in a phenocopy of monogenic defects of interleukin-10 signaling in children and may be associated with inflammatory bowel disease (IBD). The allele HLA-DRB1*01:03 is the strongest genetic risk factor for ulcerative colitis. METHODS: We used a cellular interleukin-10 reporter assay and a confirmatory competitive enzyme-linked immunosorbent assay to assess neutralizing interleukin-10 autoantibodies in serum samples obtained from patients with IBD in the Oxford and U.K. IBD BioResource cohorts and from persons without IBD (controls). An in vitro cytokine-release bioassay was performed in a subgroup of patients to assess interleukin-10, interleukin-23, interleukin-1β, tumor necrosis factor, and interleukin-6. We performed HLA association analysis using imputation and high-resolution sequencing. RESULTS: ). CONCLUSIONS: Neutralizing interleukin-10 autoantibodies were present in a subgroup of patients with IBD and were strongly associated with HLA-DRB1*01:03. (Funded by the National Institute for Health and Care Research and others.).

Fields of Study & Subjects

Inflammatory Bowel Disease Liver Diseases and Immunity Microscopic Colitis

Publication details

Journal / source
New England Journal of Medicine
Publisher
Massachusetts Medical Society
Volume
394
Issue
22
Pages
2212–2222
Publication date
10 June 2026
Language
EN