P09.14 The role of IDO1 and cellular senescence in the efficacy of PD-1 pathway blockade and radiotherapy in aged mice with glioblastoma. (21st September 2022)
- Record Type:
- Journal Article
- Title:
- P09.14 The role of IDO1 and cellular senescence in the efficacy of PD-1 pathway blockade and radiotherapy in aged mice with glioblastoma. (21st September 2022)
- Main Title:
- P09.14 The role of IDO1 and cellular senescence in the efficacy of PD-1 pathway blockade and radiotherapy in aged mice with glioblastoma
- Authors:
- Asimakidou, E
Bell, A
Bommi, P
Wainwright, D - Abstract:
- Abstract : Background: Glioblastoma is the most common primary brain tumor in adults with a median overall survival between twelve to fifteen months. 1, 2 The prognosis is worse for patients older than 65 years of age. 3 Aging is associated with senescence, which leads to secretion of proinflammatory cytokines and increased levels of the immunosuppressive enzyme indoleamine-2, 3-dioxygenase 1 (IDO1). 4 Increased levels of IDO1 at an advanced age may attenuate the efficacy of immunotherapy. Materials and Methods: One hundred and seven mice between 79 and 92 weeks of age with differential Ido1 expression were intracranially injected with syngeneic murine GL261 cells and treated with PD-1 monoclonal antibodies and radiotherapy. The mice have been monitored for ninety days. U87 glioblastoma cells were cultured and treated with interferon-γ and NU223612 . Results: PD-1 blockade and irradiation were less effective when Ido1 expression was preserved. Mouse lines with Ido1 knockout in dendritic and endothelial cells had better survival. There was a higher senescent cell burden within the brain tumor than the extra-tumoral tissue in mice reaching the humane endpoint. In U87 glioblastoma cells, interferon-γ induced upregulation of PD-L1 and IDO1 in a similar pattern. IDO1 degradation resulted in concomitantly lower levels of PD-L1. Conclusions: Taken together, these results suggest that the treatment protocol with PD-1 pathway blockade plus radiotherapy should be combined with IDO1Abstract : Background: Glioblastoma is the most common primary brain tumor in adults with a median overall survival between twelve to fifteen months. 1, 2 The prognosis is worse for patients older than 65 years of age. 3 Aging is associated with senescence, which leads to secretion of proinflammatory cytokines and increased levels of the immunosuppressive enzyme indoleamine-2, 3-dioxygenase 1 (IDO1). 4 Increased levels of IDO1 at an advanced age may attenuate the efficacy of immunotherapy. Materials and Methods: One hundred and seven mice between 79 and 92 weeks of age with differential Ido1 expression were intracranially injected with syngeneic murine GL261 cells and treated with PD-1 monoclonal antibodies and radiotherapy. The mice have been monitored for ninety days. U87 glioblastoma cells were cultured and treated with interferon-γ and NU223612 . Results: PD-1 blockade and irradiation were less effective when Ido1 expression was preserved. Mouse lines with Ido1 knockout in dendritic and endothelial cells had better survival. There was a higher senescent cell burden within the brain tumor than the extra-tumoral tissue in mice reaching the humane endpoint. In U87 glioblastoma cells, interferon-γ induced upregulation of PD-L1 and IDO1 in a similar pattern. IDO1 degradation resulted in concomitantly lower levels of PD-L1. Conclusions: Taken together, these results suggest that the treatment protocol with PD-1 pathway blockade plus radiotherapy should be combined with IDO1 inhibitors and potentially with senolytics to achieve a better therapeutic outcome in the elderly population with glioblastoma. References: Wen PY, Kesari S. Malignant gliomas in adults. New England Journal of Medicine 2008 Jul 31;359 (5):492–507. Delgado-López PD, Corrales-García EM. Survival in glioblastoma: a review on the impact of treatment modalities. Clinical and Translational Oncology 2016 Nov;18 (11):1062–71. Ladomersky E, Scholtens DM, Kocherginsky M, et al . The coincidence between increasing age, immunosuppression, and the incidence of patients with glioblastoma. Frontiers in pharmacology 2019 Mar 27;10 :200. Ladomersky E, Zhai L, Lauing KL, et al . Advanced Age Increases Immunosuppression in the Brain and Decreases Immunotherapeutic Efficacy in Subjects with Glioblastoma. Clin Cancer Res 2020 Oct 1;26 (19):5232–5245. Disclosure Information: E. Asimakidou: None. A. Bell: None. P. Bommi: None. D. Wainwright: None. … (more)
- Is Part Of:
- Journal for immunotherapy of cancer. Volume 10(2022)Supplement 1
- Journal:
- Journal for immunotherapy of cancer
- Issue:
- Volume 10(2022)Supplement 1
- Issue Display:
- Volume 10, Issue 1 (2022)
- Year:
- 2022
- Volume:
- 10
- Issue:
- 1
- Issue Sort Value:
- 2022-0010-0001-0000
- Page Start:
- A39
- Page End:
- A39
- Publication Date:
- 2022-09-21
- Subjects:
- Cancer -- Immunotherapy -- Periodicals
Cancer -- Immunological aspects -- Periodicals
Tumors -- Immunological aspects -- Periodicals
Immunotherapy -- Periodicals
616.99406105 - Journal URLs:
- http://www.immunotherapyofcancer.org ↗
https://jitc.bmj.com/ ↗
http://link.springer.com/ ↗ - DOI:
- 10.1136/jitc-2022-ITOC9.70 ↗
- Languages:
- English
- ISSNs:
- 2051-1426
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24104.xml