| Literature DB >> 18835037 |
Sandrine d'Argouges1, Sandra Wissing, Christian Brandl, Nadja Prang, Ralf Lutterbuese, Alex Kozhich, Joann Suzich, Mathias Locher, Peter Kiener, Peter Kufer, Robert Hofmeister, Patrick A Baeuerle, Ralf C Bargou.
Abstract
We have compared the cytotoxic activity of rituximab with that of blinatumomab (MT103/MEDI-538), a single-chain CD19-/CD3-bispecific antibody engaging human T cells. Blinatumomab consistently led to a higher degree of lysis of human lymphoma lines than rituximab, and was active at much lower concentration. The cytotoxicity mediated by blinatumomab and rituximab both caused a potent activation of pro-caspases 3 and 7 in target cells, a key event in induction of granzyme-mediated apoptotic cell death. Combination of rituximab with blinatumomab was found to greatly enhance the activity of rituximab, in particular at low effector-to-target cell ratios and at low antibody concentration.Entities:
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Year: 2008 PMID: 18835037 DOI: 10.1016/j.leukres.2008.08.025
Source DB: PubMed Journal: Leuk Res ISSN: 0145-2126 Impact factor: 3.156