| Literature DB >> 33627401 |
Katarzyna C Pituch1, Markella Zannikou1, Liliana Ilut1, Ting Xiao1, Michael Chastkofsky1, Madina Sukhanova2, Nicola Bertolino3, Daniele Procissi3, Christina Amidei1, Craig M Horbinski1,2, Karen S Aboody4, C David James1, Maciej S Lesniak1, Irina V Balyasnikova5.
Abstract
Glioblastoma (GBM) is the most lethal primary brain tumor in adults. No treatment provides durable relief for the vast majority of GBM patients. In this study, we've tested a bispecific antibody comprised of single-chain variable fragments (scFvs) against T cell CD3ε and GBM cell interleukin 13 receptor alpha 2 (IL13Rα2). We demonstrate that this bispecific T cell engager (BiTE) (BiTELLON) engages peripheral and tumor-infiltrating lymphocytes harvested from patients' tumors and, in so doing, exerts anti-GBM activity ex vivo. The interaction of BiTELLON with T cells and IL13Rα2-expressing GBM cells stimulates T cell proliferation and the production of proinflammatory cytokines interferon γ (IFNγ) and tumor necrosis factor α (TNFα). We have modified neural stem cells (NSCs) to produce and secrete the BiTELLON (NSCLLON). When injected intracranially in mice with a brain tumor, NSCLLON show tropism for tumor, secrete BiTELLON, and remain viable for over 7 d. When injected directly into the tumor, NSCLLON provide a significant survival benefit to mice bearing various IL13Rα2+ GBMs. Our results support further investigation and development of this therapeutic for clinical translation.Entities:
Keywords: GBM; bispecific T cell engagers; delivery; immunotherapy; neural stem cells
Year: 2021 PMID: 33627401 PMCID: PMC7936285 DOI: 10.1073/pnas.2015800118
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205