T-cell-mediated lysis of B cells induced by a CD19xCD3 bispecific single-chain antibody is perforin dependent and death receptor independent

Springer Science and Business Media LLC - Tập 53 - Trang 625-632 - 2004
Michael Gruen1,2,3, Kurt Bommert4, Ralf C. Bargou1,5,6
1Department of Hematology, Oncology and Tumorimmunology, Robert Rössle Clinic, Charité, Humboldt University of Berlin, Berlin, Germany
2Max-Delbrück Center for Molecular Medicine, Berlin, Germany
3Research Unit Molecular Cell Biology, University of Jena, Jena, Germany
4Max-Delbrück-Center for Molecular Medicine, Berlin, Germany
5Max Delbrück Center for Molecular Medicine, Berlin, Germany
6Helios Klinikum Berlin-Buch, Berlin, Germany

Tóm tắt

A recently developed bispecific antibody construct, directed against CD19 and CD3 (bscCD19xCD3), induces T-cell-mediated lysis of allogeneic and autologous B cells in a specific and highly efficient manner. Since knowledge of the molecular mechanisms underlying this lysis is limited, a study on bscCD19xCD3-activated T-cell-effector pathways was performed. BscCD19xCD3-induced lysis of target B-cell lines Nalm-6, Daudi, and Raji and of autologous primary B cells is caused by the perforin-dependent granule-exocytosis pathway but not by the death ligands FasL, TRAIL, or TNF-α. When activated by bscCD19xCD3 and Raji cells, T cells express FasL mRNA, but incubation of Raji cells with cell-free supernatants from cytotoxicity experiments caused an upregulation of c-Flipl, possibly accounting for the cells’ insensitivity toward death-receptor-mediated lysis. In addition to granule exocytosis, Raji cells are lysed by at least one mechanism independent of perforin, which requires transport through the T cell’s Golgi apparatus.

Tài liệu tham khảo

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