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Cutting Edge: IL-21 Is a Switch Factor for the Production of IgG1 and IgG3 by Human B Cells
Author(s) -
Jérôme Pène,
JeanFrançois Gauchat,
Sandrine Lécart,
Élodie Drouet,
Paul Guglielmi,
Véra Boulay,
Adriana Delwail,
Don Foster,
JeanClaude Lecron,
Hans Yssel
Publication year - 2004
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.172.9.5154
Subject(s) - cd19 , cd40 , cytidine deaminase , immunoglobulin class switching , microbiology and biotechnology , biology , stimulation , antibody , b cell , cytokine , immunology , cytotoxic t cell , in vitro , endocrinology , biochemistry
IL-21 is a cytokine that regulates the activation of T and NK cells and promotes the proliferation of B cells activated via CD40. In this study, we show that rIL-21 strongly induces the production of all IgG isotypes by purified CD19(+) human spleen or peripheral blood B cells stimulated with anti-CD40 mAb. Moreover, it was found to specifically induce the production of IgG(1) and IgG(3) by CD40-activated CD19(+)CD27(-) naive human B cells. Although stimulation of CD19(+) B cells via CD40 alone induced gamma 1 and gamma 3 germline transcripts, as well as the expression of activation-induced cytidine deaminase, only stimulation with both anti-CD40 mAb and rIL-21 resulted in the production of S gamma/S mu switch circular DNA. These results show that IL-21, in addition to promoting growth and differentiation of committed B cells, is a specific switch factor for the production of IgG(1) and IgG(3).

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