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COMMENTARY |
CORRESPONDENCE D.T.: tarlinton{at}wehi.edu.au
ABSTRACT
Antibody diversity is first generated by rearrangement of immunoglobulin (Ig) genes during B cell development in the bone marrow, and later by antigen-driven diversification in germinal centers (GCs). New data in humans and mice now identify specific B cell populations that may have undergone antigen-independent hypermutation outside GCs.
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