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Strong Clonal Relatedness between Serum and Gut IgA despite Different Plasma Cell Origins
Author(s) -
Rasmus Iversen,
Omri Snir,
Maria Stensland,
José Eduardo Kroll,
Øyvind Steinsbø,
Ilma R. Korponay–Szabó,
Knut E.A. Lundin,
Gustavo A. de Souza,
Ludvig M. Sollid
Publication year - 2017
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2017.08.036
Subject(s) - antibody , immunoglobulin a , biology , lamina propria , antigen , immunology , j chain , secretory component , secretion , immunoglobulin g , epithelium , genetics , endocrinology
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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