4.8 Article

Strong Clonal Relatedness between Serum and Gut IgA despite Different Plasma Cell Origins

期刊

CELL REPORTS
卷 20, 期 10, 页码 2357-2367

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CELL PRESS
DOI: 10.1016/j.celrep.2017.08.036

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资金

  1. Research Council of Norway through its Centre of Excellence [179573/V40]
  2. South-Eastern Norway Regional Health Authority [2011050, 2014045, 2016113]
  3. European Commission [ERC-2010-Ad-268541, FP6-2005-FOOD-4B-36383]
  4. Stiftelsen KG Jebsen [SKGH-MED-017]
  5. Hungarian National Research Fund [OTKA K101788]

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Mucosal antigens induce generation of lamina propria plasma cells (PCs) that secrete dimeric immunoglobulin A (IgA) destined for transport across the epithelium. In addition, blood contains monomeric IgA. To study the relationship between mucosal and systemic antibody responses, we took advantage of celiac disease patient samples for isolation of gut PCs as well as serum IgA and IgG reactive with a gluten-derived peptide or the autoantigen transglutaminase 2. Proteomic analysis of serum IgA revealed antigen-specific V-gene preferences, which matched those found in gut PCs. Further, gut PC CDR-H3 sequences were abundant in serum IgA but also detectable in serum IgG. Our data indicate that the same B cell clones that give rise to gut PCs also contribute to the serum antibody pool. However, serum IgA antibodies had a molecular composition distinct from that of IgA antibodies secreted in the gut, suggesting that individual B cell clones give rise to different PC populations.

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