Switchable CAR-T cells mediate remission in metastatic pancreatic ductal adenocarcinoma. Issue 6 (18th August 2018)
- Record Type:
- Journal Article
- Title:
- Switchable CAR-T cells mediate remission in metastatic pancreatic ductal adenocarcinoma. Issue 6 (18th August 2018)
- Main Title:
- Switchable CAR-T cells mediate remission in metastatic pancreatic ductal adenocarcinoma
- Authors:
- Raj, Deepak
Yang, Ming-Hsin
Rodgers, David
Hampton, Eric N
Begum, Julfa
Mustafa, Arif
Lorizio, Daniela
Garces, Irene
Propper, David
Kench, James G
Kocher, H M
Young, Travis S
Aicher, Alexandra
Heeschen, Christopher - Abstract:
- Abstract : Objective: Pancreatic ductal adenocarcinoma (PDAC) is a disease of unmet medical need. While immunotherapy with chimeric antigen receptor T (CAR-T) cells has shown much promise in haematological malignancies, their efficacy for solid tumours is challenged by the lack of tumour-specific antigens required to avoid on-target, off-tumour effects. Switchable CAR-T cells whereby activity of the CAR-T cell is controlled by dosage of a tumour antigen-specific recombinant Fab-based 'switch' to afford a fully tunable response may overcome this translational barrier. Design: In this present study, we have used conventional and switchable CAR-T cells to target the antigen HER2, which is upregulated on tumour cells, but also present at low levels on normal human tissue. We used patient-derived xenograft models derived from patients with stage IV PDAC that mimic the most aggressive features of PDAC, including severe liver and lung metastases. Results: Switchable CAR-T cells followed by administration of the switch directed against human epidermal growth factor receptor 2 (HER2)-induced complete remission in difficult-to-treat, patient-derived advanced pancreatic tumour models. Switchable HER2 CAR-T cells were as effective as conventional HER2 CAR-T cells in vivo testing a range of different CAR-T cell doses. Conclusion: These results suggest that a switchable CAR-T system is efficacious against aggressive and disseminated tumours derived from patients with advanced PDAC whileAbstract : Objective: Pancreatic ductal adenocarcinoma (PDAC) is a disease of unmet medical need. While immunotherapy with chimeric antigen receptor T (CAR-T) cells has shown much promise in haematological malignancies, their efficacy for solid tumours is challenged by the lack of tumour-specific antigens required to avoid on-target, off-tumour effects. Switchable CAR-T cells whereby activity of the CAR-T cell is controlled by dosage of a tumour antigen-specific recombinant Fab-based 'switch' to afford a fully tunable response may overcome this translational barrier. Design: In this present study, we have used conventional and switchable CAR-T cells to target the antigen HER2, which is upregulated on tumour cells, but also present at low levels on normal human tissue. We used patient-derived xenograft models derived from patients with stage IV PDAC that mimic the most aggressive features of PDAC, including severe liver and lung metastases. Results: Switchable CAR-T cells followed by administration of the switch directed against human epidermal growth factor receptor 2 (HER2)-induced complete remission in difficult-to-treat, patient-derived advanced pancreatic tumour models. Switchable HER2 CAR-T cells were as effective as conventional HER2 CAR-T cells in vivo testing a range of different CAR-T cell doses. Conclusion: These results suggest that a switchable CAR-T system is efficacious against aggressive and disseminated tumours derived from patients with advanced PDAC while affording the potential safety of a control switch. … (more)
- Is Part Of:
- Gut. Volume 68:Issue 6(2019)
- Journal:
- Gut
- Issue:
- Volume 68:Issue 6(2019)
- Issue Display:
- Volume 68, Issue 6 (2019)
- Year:
- 2019
- Volume:
- 68
- Issue:
- 6
- Issue Sort Value:
- 2019-0068-0006-0000
- Page Start:
- 1052
- Page End:
- 1064
- Publication Date:
- 2018-08-18
- Subjects:
- pancreatic cancer -- stem cells -- immunotherapy -- liver metastases
Gastroenterology -- Periodicals
616.33 - Journal URLs:
- http://gut.bmjjournals.com ↗
http://www.bmj.com/archive ↗ - DOI:
- 10.1136/gutjnl-2018-316595 ↗
- Languages:
- English
- ISSNs:
- 0017-5749
- 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:
- 17950.xml