Item Type: | Article |
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Title: | Cytolysis of leukemic B-cells by T-cells activated via 2 bispecific antibodies |
Creators Name: | Bohlen, H., Manzke, O., Patel, B., Moldenhauer, G., Doerken, B., von Fliedner, V., Diehl, V. and Tesch, H. |
Abstract: | Bispecific monoclonal antibodies can be used in the activation of effector cells to lyse autologous tumor cells. We analyzed the activation of human T-cells in vitro with bispecific monoclonal antibodies, which were generated by hybridoma-hybridoma fusion. Preactivated allogeneic and autologous T-cells could be triggered to lyse tumoral B-cells in the presence of CD3 x CD19 bispecific antibodies. In addition, the combined use of two CD3 x CD19 plus CD28 x CD22 bispecific antibodies induced optimal interleukin 2 secretion by Jurkat T-cell acute lymphocytic leukemia cells in the presence of target B-cells. The same antibody combination was able to generate cytolytic effector cells without prior activation, when resting T-cells were cocultured with freshly isolated autologous leukemic B-cells in the presence of the bispecific antibodies. The results suggest that signals required to activate cytolytic T-cell precursors can be provided by the two bispecific antibodies. Although activation of resting T-cells can be achieved by CD3 x CD19 bispecific antibodies in association with monospecific bivalent CD28 antibodies, the second bispecific antibody, CD28 x CD22, further increases the specificity of the target cell dependent activation of T-cells. When used for immunotherapy of B-cell malignancies, the CD3 x CD19 and CD28 x CD22 bispecific antibody combination may avoid the need for ex vivo activated effector cells, because the antibodies may induce T-cell activation directly at the tumor site. |
Keywords: | Monoclonal Antibodies, Antibody Specificity, CD Antigens, B-Lymphocyte Differentiation Antigens, T-Lymphocyte Differentiation Antigens, Cell Adhesion Molecules, Immunologic Cytotoxicity, Lectins, B-Cell Leukemia, Lymphocyte Activation, Cytotoxic T-Lymphocytes, Cultured Tumor Cells, Animals, Mice |
Source: | Cancer Research |
ISSN: | 0008-5472 |
Publisher: | American Association for Cancer Research |
Volume: | 53 |
Number: | 18 |
Page Range: | 4310-4314 |
Date: | 15 September 1993 |
Official Publication: | http://cancerres.aacrjournals.org/content/53/18/4310.abstract |
PubMed: | View item in PubMed |
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