Cutting Edge: Transitional T3 B Cells Do Not Give Rise to Mature B Cells, Have Undergone Selection, and Are Reduced in Murine Lupus
Author(s) -
Brittany N. Teague,
Yujun Pan,
Philip A. Mudd,
Britt Nakken,
Qingzhao Zhang,
Péter Szodoray,
Xana Kim-Howard,
Patrick C. Wilson,
A. Darise Farris
Publication year - 2007
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.178.12.7511
Subject(s) - b cell , biology , systemic lupus erythematosus , microbiology and biotechnology , autoimmunity , immunology , b cell receptor , breakpoint cluster region , antibody , receptor , medicine , genetics , disease
As the immediate precursors to mature follicular B cells in splenic development, immature transitional cells are an essential component for understanding late B cell differentiation. It has been shown that T2 cells can give rise to mature B cells; however, whether T3 B cells represent a normal stage of B cell development, which has been widely assumed, has not been fully resolved. In this study, we demonstrate both in vitro and in vivo that T3 B cells do not give rise to mature B cells and are instead selected away from the T1-->T2-->mature B cell developmental pathway and are hyporesponsive to stimulation through the BCR. Significantly reduced numbers of T3 B cells in young lupus-prone mice further suggest that the specificity of this subset holds clues to understanding autoimmunity.
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