Abstract
Human B lymphocyte ontogeny and differentiation has been traditionally studied by the sequential expression of a series of B cell markers including heavy chain isotypes of immunoglobulin [1, 2], HLA-D-related Ia-like antigens [3–5], receptors for complement components [6, 7] and for the Fc portion of immunoglobulin [8, 9], and receptors for murine and monkey erythrocytes [10, 11]. Although these markers have provided insight into the stages of normal B cell differentiation, their utility has been limited because they are also expressed on cells of other lineages. The development of monoclonal antibodies which identify unique B cell-associated antigens has already begun to provide a series of new reagents to more precisely study the sequence of normal human B cell differentiation.
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Nadler, L.M., Anderson, K.C., Bates, M., Park, E., Slaughenhoupt, B., Schlossman, S.F. (1984). Human B Cell-Associated Antigens: Expression on Normal and Malignant B Lymphocytes. In: Bernard, A., Boumsell, L., Dausset, J., Milstein, C., Schlossman, S.F. (eds) Leucocyte Typing. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-68857-7_25
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DOI: https://doi.org/10.1007/978-3-642-68857-7_25
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