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Ida Lindeman

@idalindeman.bsky.social
131 followers 417 following 5 posts

Postdoc at the University of Oslo. Interested in autoimmunity, celiac disease, rheumatoid arthritis, plasma cells, BCRs, TCRs, IG and TR polymorphisms and single-cell technologies.

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Reposted by Ida Lindeman
Rasmus Iversen @rasmusi.bsky.social · 27/07/2026
Happy to see our paper on systemic and gut IgA out now in @cp-cellreports.bsky.social! www.cell.com/cell-reports...
cell.com
Distinct systemic and gut IgA responses to bacteria of the human upper gastrointestinal tract
The relationship between mucosal and systemic IgA is not well understood. Vaz et al. show that serum IgA targets bacteria of the upper gastrointestinal tract and that IgA-expressing plasma cells in bo...
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Ida Lindeman @idalindeman.bsky.social · 02/07/2026
Thanks to everyone involved in this study! @aenguso.bsky.social, @cdubsig.bsky.social, Eivind Ness-Jensen, Ludvig Sollid, @uio.no, Oslo University Hospital, NTNU
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Ida Lindeman @idalindeman.bsky.social · 02/07/2026
Our results offer a new angle on genetic risk and pathogenesis in celiac disease. Which other HLA-associated diseases could be affected by skewed naive TCR repertoires?
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Ida Lindeman @idalindeman.bsky.social · 02/07/2026
We observed a particularly strong effect of the HLA-DQ2.5-DR3 haplotype on TCR V gene usage, skewing the repertoire toward known gluten–HLA-DQ2.5–reactive TCRs. This links HLA polymorphisms to both antigen presentation and TCR repertoire selection.
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Ida Lindeman @idalindeman.bsky.social · 02/07/2026
We bulk sequenced naive CD4+ alpha beta TCR repertoires from 103 celiac patients and 103 controls, and additionally genotyped most of these. Gene usage quantitative trait loci analyses revealed a strong impact of both polymorphisms within the TCR loci (TRA/TRB) and the HLA region on TCR gene usage.
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Ida Lindeman @idalindeman.bsky.social · 02/07/2026
🔔Our new PNAS study shows that celiac disease-associated HLA-DQ2.5 doesn’t just present gluten—it preselects naive TCRs that can recognize gluten. HLA risk alleles help wire a disease-relevant T cell repertoire before antigen exposure. #autoimmunity #TCR #celiac #HLA 🧵 www.pnas.org/doi/10.1073/...
pnas.org
PNAS
Proceedings of the National Academy of Sciences (PNAS), a peer reviewed journal of the National Academy of Sciences (NAS) - an authoritative source of high-impact, original research that broadly spans...
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Reposted by Ida Lindeman
Rasmus Iversen @rasmusi.bsky.social · 07/07/2025
Very happy to share our latest preprint, where we address the relationship between systemic and gut IgA. See link below and details in 🧵. Huge thanks to everyone involved! www.biorxiv.org/content/10.1...
biorxiv.org
Distinct systemic and gut IgA responses to bacteria of the human upper gastrointestinal tract
The mucosa lining the gastrointestinal tract harbors the body's largest population of plasma cells, most of which produce dimeric IgA destined for release into the lumen. In addition, there is systemic production of monomeric IgA circulating in the blood. Little is known about the connection between systemic and mucosal IgA. To address this relationship and to explore antibody responses against the microbiota, we isolated bacteria from duodenal biopsies and assessed antibody reactivity. Systemic IgA showed reactivity to bacteria of the upper gastrointestinal tract with a preference for binding Neisseria species, while duodenal IgA showed broader reactivity. We found limited clonal overlap between gut and bone marrow plasma cells of individual donors, yet a few shared clones specific to bacterial antigens were identified. Despite showing clonal overlap, gut and bone marrow plasma cells have distinct IgA subclass distributions, and they likely depend on B-cell activation at discrete anatomical sites. ### Competing Interest Statement The authors have declared no competing interest. Kristian Gerhard Jebsen Foundation, https://ror.org/021g6tq38, SKGJ-MED-017 Southern and Eastern Norway Regional Health Authority, https://ror.org/02qx2s478, 2022071 University of Oslo, https://ror.org/01xtthb56, WL-IMMUNOLOGY, Scientia Fellows II
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