Abstract
Monoclonal antibodies (MoAb) directed to differentiation antigens on human leucocytes have proved to be extremely valuable tools for the dissection of the immune system. It has become clear that the expression of unique surface determinants on certain immunoregulatory cells apparently correlates with function in the regulatory network of cell interactions. In our attempt to raise MoAb against differentiation antigens on mature T lymphocytes, mice were immunized with homogeneous leukemic cell populations obtained from patients suffering from chronic lymphocytic leukemia (CLL) of T type. This strategy was based on the idea that the leukemic cells of a T-CLL might be the clonally expanded, well-differentiated malignant counterpart of a normal T cell phenotype representing a distinct functional subset.
Part of this work was supported by the Deutsche Forschungsgemeinschaft, Bonn, Sonderforschungsbereich 37 and by the Curt-Bohnewand-Fonds, University of Munich
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© 1984 Springer-Verlag Berlin Heidelberg
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Rieber, P. et al. (1984). Characterization of Functional Human T Cell Subsets by Monoclonal Antibodies. 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_18
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DOI: https://doi.org/10.1007/978-3-642-68857-7_18
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