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Ultra long-lived plasma cells in the human small intestine produce microbiota-reactive IgA antibodies

Pati, N. B.; Chung, B. K.; Holm, K.; Saetre, F.; Reims, H. M.; Aasebo, A. T.; Gedde-Dahl, T.; Domanska, D.; Hov, J. R.; Baekkevold, E. S.; Jahnsen, F. L.

2025-03-17 immunology
10.1101/2025.03.17.643697 bioRxiv
Show abstract

A large fraction of the intestinal microbiota is highly coated with secretory IgA, and bacteria-specific IgA is believed to shape the composition of the microbiota. A hallmark of the adaptive immune system is immunological memory to specific antigens. However, whether there is strong and persistent memory of secretory antibodies to bacterial antigens has not been determined. Here we show that ultra long-lived CD19- CD45- (age>20 years) plasma cells (PCs) residing in the human small intestine produce IgA that binds to most taxa of a diverse anaerobic microbiota culture. Long-lived CD19-CD45+ (age>10 years) and short-lived CD19+CD45+ (age<2 years) PCs also produced IgA with broad bacterial reactivity. A clear correlation between high-binding and low-binding taxa was observed across the PC subsets. We also found that host PCs were depleted in acute intestinal graft versus host disease, a condition strongly associated with loss of microbiota diversity. Together, we show that bacterial antigens in the intestine induce an extremely stable, long-lasting humoral immune memory that may be important for the long-term stability and resilience of the intestinal microbiome.

Published in Beneficial Microbes · not in our set (fewer than 10 published preprints to learn from) · training set

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