Impairment of T-cell-dependent B-cell responses and B-l cell development in CD19-deficient mice

• DOI: 10.1038/376352a0
• Publication Date: 2003-08-12T01:37:00Z
• Authors: Robert C. Rickert; Klaus Rajewsky; Jiirgen Roes
• Keywords: 0301 basic medicine; B-Lymphocytes; Mice, Inbred BALB C; Base Sequence; Antigens, CD19; Molecular Sequence Data; B-Lymphocyte Subsets; Bone Marrow Cells; Cell Differentiation; Flow Cytometry; Hematopoietic Stem Cells; Lymphocyte Activation; Antigens, Differentiation, B-Lymphocyte; Mice; 03 medical and health sciences; Antigens, CD; Mutagenesis; Animals; Antigens; Peritoneal Cavity; Cells, Cultured; DNA Primers

CD19 is the hallmark differentiation antigen of the B lineage. Its early expression has implicated a role for CD19 during the antigen-independent phases of B-cell development, whereas in mature B cells CD19 can act synergistically with surface immunoglobulin to induce activation. We have generated CD19-deficient mice and found that development of conventional B cells is unperturbed. However, mature CD19-/- B cells show a profound deficiency in responding to protein antigens that require T-cell help. This is accompanied by a lack of germinal centre formation and affinity maturation of serum antibodies. Thus CD19 is crucial for both initial B-cell activation by T-cell-dependent antigens and the maturation and/or selection of the activated cells into the memory compartment. An impairment in ligand-driven selection may also be responsible for the observation of a striking reduction in the B-1 (formerly Ly-1) B-cell subset, thought to develop under the control of self-antigens and bacterial antigens (reviewed in ref. 2).