Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Gewählte Publikation:
SHR Neuro Krebs Kardio Lipid Stoffw Microb
Klawitter, M; El-Ayoubi, A; Buch, J; Rüttinger, J; Ehrenfeld, M; Lichtenegger, E; Krüger, MA; Mantwill, K; Koll, FJ; Kowarik, MC; Holm, PS; Naumann, U.
The Oncolytic Adenovirus XVir-N-31, in Combination with the Blockade of the PD-1/PD-L1 Axis, Conveys Abscopal Effects in a Humanized Glioblastoma Mouse Model.
Int J Mol Sci. 2022; 23(17):
Doi: 10.3390/ijms23179965
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- Co-Autor*innen der Med Uni Graz
- Koll Florestan Johannes
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- Abstract:
- Glioblastoma (GBM) is an obligatory lethal brain tumor with a median survival, even with the best standard of care therapy, of less than 20 months. In light of this fact, the evaluation of new GBM treatment approaches such as oncolytic virotherapy (OVT) is urgently needed. Based on our preliminary preclinical data, the YB-1 dependent oncolytic adenovirus (OAV) XVir-N-31 represents a promising therapeutic agent to treat, in particular, therapy resistant GBM. Preclinical studies have shown that XVir-N-31 prolonged the survival of GBM bearing mice. Now using an immunohumanized mouse model, we examined the immunostimulatory effects of XVir-N-31 in comparison to the wildtype adenovirus (Ad-WT). Additionally, we combined OVT with the inhibition of immune checkpoint proteins by using XVir-N-31 in combination with nivolumab, or by using a derivate of XVir-N-31 that expresses a PD-L1 neutralizing antibody. Although in vitro cell killing was higher for Ad-WT, XVir-N-31 induced a much stronger immunogenic cell death that was further elevated by blocking PD-1 or PD-L1. In vivo, an intratumoral injection of XVir-N-31 increased tumor infiltrating lymphocytes (TILs) and NK cells significantly more than Ad-WT not only in the virus-injected tumors, but also in the untreated tumors growing in the contralateral hemisphere. This suggests that for an effective treatment of GBM, immune activating properties by OAVs seem to be of greater importance than their oncolytic capacity. Furthermore, the addition of immune checkpoint inhibition (ICI) to OVT further induced lymphocyte infiltration. Consequently, a significant reduction in contralateral non-virus-injected tumors was only visible if OVT was combined with ICI. This strongly indicates that for an effective eradication of GBM cells that cannot be directly targeted by an intratumoral OV injection, additional ICI therapy is required.
- Find related publications in this database (using NLM MeSH Indexing)
- Adenoviridae - genetics, metabolism
- Animals - administration & dosage
- B7-H1 Antigen - genetics, metabolism
- Cell Line, Tumor - administration & dosage
- Disease Models, Animal - administration & dosage
- Glioblastoma - metabolism
- Mice - administration & dosage
- Oncolytic Virotherapy - administration & dosage
- Programmed Cell Death 1 Receptor - administration & dosage
- Find related publications in this database (Keywords)
- glioblastoma
- oncolytic virotherapy
- immune checkpoint inhibition
- abscopal effects
- XVir-N-31