Enhanced AC133-specific CAR T cell therapy induces durable remissions in mice with metastatic small cell lung cancer. (10th July 2022)
- Record Type:
- Journal Article
- Title:
- Enhanced AC133-specific CAR T cell therapy induces durable remissions in mice with metastatic small cell lung cancer. (10th July 2022)
- Main Title:
- Enhanced AC133-specific CAR T cell therapy induces durable remissions in mice with metastatic small cell lung cancer
- Authors:
- Taromi, Sanaz
Firat, Elke
Simonis, Alexander
Braun, Lukas M.
Apostolova, Petya
Elze, Mirjam
Passlick, Bernward
Schumacher, Alicia
Lagies, Simon
Frey, Anna
Schmitt-Graeff, Annette
Burger, Meike
Schmittlutz, Katrin
Follo, Marie
von Elverfeldt, Dominik
Zhu, Xuekai
Kammerer, Bernd
Diederichs, Sven
Duyster, Justus
Manz, Markus G.
Niedermann, Gabriele
Zeiser, Robert - Abstract:
- Abstract: Metastatic small cell lung cancer (SCLC) is not curable. While SCLC is initially sensitive to chemotherapy, remissions are short-lived. The relapse is induced by chemotherapy-selected tumor stem cells, which express the AC133 epitope of the CD133 stem cell marker. We studied the effectiveness of AC133-specific CAR T cells post-chemotherapy using human primary SCLC and an orthotopic xenograft mouse model. AC133-specific CAR T cells migrated to SCLC tumor lesions, reduced the tumor burden, and prolonged survival in a humanized orthotopic SCLC model, but were not able to entirely eliminate tumors. We identified CD73 and PD-L1 as immune-escape mechanisms and combined PD-1-inhibition and CD73-inhibition with CAR T cell treatment. This triple-immunotherapy induced cures in 25% of the mice, without signs of graft-versus-host disease or bone marrow failure. AC133 + cancer stem cells and PD-L1 + CD73 + myeloid cells were detectable in primary human SCLC tissues, suggesting that patients may benefit from the triple-immunotherapy. We conclude that the combination of AC133-specific CAR T cells, anti-PD-1-antibody and CD73-inhibitor specifically eliminates chemo-resistant tumor stem cells, overcomes SCLC-mediated T cell inhibition, and might induce long-term complete remission in an otherwise incurable disease. Highlights: AC133-specific CAR T cells eliminate cancer stem cells. Orthotopic SCLC mouse model reflects the clinical course of human metastatic SCLC. CD73 and PD-L1Abstract: Metastatic small cell lung cancer (SCLC) is not curable. While SCLC is initially sensitive to chemotherapy, remissions are short-lived. The relapse is induced by chemotherapy-selected tumor stem cells, which express the AC133 epitope of the CD133 stem cell marker. We studied the effectiveness of AC133-specific CAR T cells post-chemotherapy using human primary SCLC and an orthotopic xenograft mouse model. AC133-specific CAR T cells migrated to SCLC tumor lesions, reduced the tumor burden, and prolonged survival in a humanized orthotopic SCLC model, but were not able to entirely eliminate tumors. We identified CD73 and PD-L1 as immune-escape mechanisms and combined PD-1-inhibition and CD73-inhibition with CAR T cell treatment. This triple-immunotherapy induced cures in 25% of the mice, without signs of graft-versus-host disease or bone marrow failure. AC133 + cancer stem cells and PD-L1 + CD73 + myeloid cells were detectable in primary human SCLC tissues, suggesting that patients may benefit from the triple-immunotherapy. We conclude that the combination of AC133-specific CAR T cells, anti-PD-1-antibody and CD73-inhibitor specifically eliminates chemo-resistant tumor stem cells, overcomes SCLC-mediated T cell inhibition, and might induce long-term complete remission in an otherwise incurable disease. Highlights: AC133-specific CAR T cells eliminate cancer stem cells. Orthotopic SCLC mouse model reflects the clinical course of human metastatic SCLC. CD73 and PD-L1 expression drives immune-escape mechanisms in human primary SCLC. The triple-immunotherapy specifically eliminates chemo-resistant tumor stem cells. The triple-immunotherapy induced cures in 25% of the mice, without signs of GVHD. … (more)
- Is Part Of:
- Cancer letters. Volume 538(2022)
- Journal:
- Cancer letters
- Issue:
- Volume 538(2022)
- Issue Display:
- Volume 538, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 538
- Issue:
- 2022
- Issue Sort Value:
- 2022-0538-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-07-10
- Subjects:
- SCLC -- CAR T cells -- CD73 -- PD-1 -- CD133
Cancer -- Periodicals
Neoplasms -- Periodicals
Cancer -- Périodiques
Electronic journals
616.994 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03043835/ ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.canlet.2022.215697 ↗
- Languages:
- English
- ISSNs:
- 0304-3835
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3046.485000
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