IL-21 effects on human IgE production in response to IL-4 or IL-13

Nancy Wood, Karen Bourque, Debra D. Donaldson, Mary Collins, Donata Vercelli, Samuel J. Goldman, Marion T. Kasaian

Research output: Contribution to journalArticlepeer-review

104 Scopus citations


In human atopic disease, IgE sensitizes the allergic response, while IgG4 is protective. Because IL-4 and IL-13 trigger switch recombination to both IgE and IgG4, additional agents must regulate the balance between these isotypes to influence susceptibility or tolerance to atopy. In this report, we define in vitro conditions leading to activation or inhibition of human IgE and IgG4 production by IL-21. IL-21 reduced IL-4-driven IgE synthesis by mitogen-stimulated human PBMC. IL-21 inhibition of human IgE production was not a direct effect on B cells, was not seen following B cell activation with IL-13, and was overcome by CD40 ligation. Neither IFN-γ, IL-10, IL-12, CD40L expression, nor apoptosis was responsible for the inhibitory effect. In contrast, IL-21-stimulated secretion of IgG4 from PBMC. Our findings indicate that IL-21 may influence the production of both human IgE and IgG4, and thus contribute to the regulation of atopic reactions.

Original languageEnglish (US)
Pages (from-to)133-145
Number of pages13
JournalCellular Immunology
Issue number1-2
StatePublished - Sep 2004


  • Allergy
  • B cells
  • Cytokines

ASJC Scopus subject areas

  • Immunology


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