DDDR-48. An AAV-1 mediated dual-payload gene therapy for high grade glioma

Abstract BACKGROUND There have been few advances in glioblastoma treatment in recent decades. Treatments fail due to tumour heterogeneity (genetic, epigenetic, cell-state) and persistence of GBM stem-like cells (GSCs) within the tumour margin. SOX2 and SOX9 are consistently overexpressed in GSCs – an exploitable commonality across diverse tumour subtypes. Cell type-specific promoters are used in gene therapy to restrict therapeutic payload expression but often have suboptimal strength, selectivity, and size. RESULTS Focusing on the core SOX-driven transcriptional regulatory network in GSCs, we engineered synthetic super-enhancers (SSEs) with robust activity and exquisite cell state selectivity. TGX-007 is an AAV-1 mediated therapy delivering a combination of cytotoxic (HSVtk) and immune-modulatory (IL12) genetic payloads under the control of our SSE. We show that TGX-007 is curative in an aggressive immunocompetent mouse glioblastoma model, without off-target toxicities and with generation of immunological memory, preventing tumour formation on re-exposure. >85% of mice treated with TGX-007 were cured; all control mice died within 50 days. Treated mice were re-exposed to tumorigenic cells at 20 weeks and none developed tumours; all control mice developed tumours and died. A clear dose-response relationship was seen between TGX-007 concentration and cure rate in mice. AAV-SSE activity and selectivity was validated using primary human GBM tissue and normal cortex. CONCLUSIONS These findings provide the rationale for a first-in-human, phase I/II Bayesian optimal interval study to establish the safety and OBD of TGX-007 and to assess preliminary efficacy of TGX-007 in patients with newly-diagnosed GBM or with first radiological progression of previously treated GBM. TGX-007 will be administered with intra-operative MRI guidance via convection enhanced delivery. Patients will then receive 2 weeks valaciclovir (HSVtk substrate) prior to surgical debulking, then standard-of-care treatment. The OBD will be selected based on toxicity and tissue activity; signal of clinical efficacy will be assessed by overall survival.

Authors

Institutions

Publication Details

Journal
Neuro-Oncology
Published
2025-11-01
DOI
https://doi.org/10.1093/neuonc/noaf201.0685
Primary Topic
Virus-based gene therapy research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

DDDR-48. An AAV-1 mediated dual-payload gene therapy for high grade glioma

Brian M. Dixon, Neza Alfazema, Paul Brennan, Christina Gertrude Yap et al.
Neuro-Oncology
Virus-based gene therapy research
article

DDDR-48. An AAV-1 mediated dual-payload gene therapy for high grade glioma

Brian M. Dixon, Neza Alfazema, Paul Brennan, Christina Gertrude Yap, José Antonio Iglesias, Russell R. Lonser, Steven M. Pollard, Faye Robertson, Krystof S. Bankiewicz, Mantas Matjusaitis, Brad Elder, Ken Macnamara, Ute Koeber
article en

Abstract

Abstract BACKGROUND There have been few advances in glioblastoma treatment in recent decades. Treatments fail due to tumour heterogeneity (genetic, epigenetic, cell-state) and persistence of GBM stem-like cells (GSCs) within the tumour margin. SOX2 and SOX9 are consistently overexpressed in GSCs – an exploitable commonality across diverse tumour subtypes. Cell type-specific promoters are used in gene therapy to restrict therapeutic payload expression but often have suboptimal strength, selectivity, and size. RESULTS Focusing on the core SOX-driven transcriptional regulatory network in GSCs, we engineered synthetic super-enhancers (SSEs) with robust activity and exquisite cell state selectivity. TGX-007 is an AAV-1 mediated therapy delivering a combination of cytotoxic (HSVtk) and immune-modulatory (IL12) genetic payloads under the control of our SSE. We show that TGX-007 is curative in an aggressive immunocompetent mouse glioblastoma model, without off-target toxicities and with generation of immunological memory, preventing tumour formation on re-exposure. >85% of mice treated with TGX-007 were cured; all control mice died within 50 days. Treated mice were re-exposed to tumorigenic cells at 20 weeks and none developed tumours; all control mice developed tumours and died. A clear dose-response relationship was seen between TGX-007 concentration and cure rate in mice. AAV-SSE activity and selectivity was validated using primary human GBM tissue and normal cortex. CONCLUSIONS These findings provide the rationale for a first-in-human, phase I/II Bayesian optimal interval study to establish the safety and OBD of TGX-007 and to assess preliminary efficacy of TGX-007 in patients with newly-diagnosed GBM or with first radiological progression of previously treated GBM. TGX-007 will be administered with intra-operative MRI guidance via convection enhanced delivery. Patients will then receive 2 weeks valaciclovir (HSVtk substrate) prior to surgical debulking, then standard-of-care treatment. The OBD will be selected based on toxicity and tissue activity; signal of clinical efficacy will be assessed by overall survival.

Neuro-OncologyVol. 27(Supplement_5)
Institute of Cancer Research (GB), TiGenix (Spain) (ES), Apogenix (Germany) (DE), The Ohio State University (US), University of Edinburgh (GB)
Openalex Percentile: Top 64%
Virus-based gene therapy research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.