Development of ROR1 CAR-T cells to target cancer stem cells in advanced malignancies
Grant Award Details
Grant Type:
Grant Number:
TRAN1-10258
Investigator(s):
Disease Focus:
Human Stem Cell Use:
Cell Line Generation:
Award Value:
$5,795,584
Status:
Closed
Progress Reports
Reporting Period:
Final Operational Milestone #3
Grant Application Details
Application Title:
Development of ROR1 CAR-T cells to target cancer stem cells in advanced malignancies
Public Abstract:
Translational Candidate
Autologous ROR1 CAR-T cell transduced with a lentiviral vector containing scFv (cirmtuzumab) with CD28, CD137, CD3zeta signaling domains
Area of Impact
ROR1 expressing cancer stem cells in solid tumors and hematologic tumors
Mechanism of Action
ROR1 CAR is a 3rd generation chimeric construct with an internal endodomain that transmits a CD3 zeta signal with added co-stimulatory signaling domains 4-1BB and CD28. When the transduced ROR-1 CAR-T cell comes into contact with its cognate receptor, a signal is transmitted by the CD3 zeta-chain, inducing lymphocyte proliferation and expression of trans-acting interleukins and chemokines that activate other immuno-reactive cells and in certain cases directly kill ROR1+ Cancer Stem Cells
Unmet Medical Need
Compelling evidence suggests that dormant cancer stem cells (CSCs) are considered the origin of therapeutic resistance, and are responsible for relapse and metastasis. We will selectively identify and attack CSCs through the ROR1 receptor, using CAR-T cells to address this unmet medical need.
Project Objective
Completion of a Pre-IND meeting
Major Proposed Activities
Autologous ROR1 CAR-T cell transduced with a lentiviral vector containing scFv (cirmtuzumab) with CD28, CD137, CD3zeta signaling domains
Area of Impact
ROR1 expressing cancer stem cells in solid tumors and hematologic tumors
Mechanism of Action
ROR1 CAR is a 3rd generation chimeric construct with an internal endodomain that transmits a CD3 zeta signal with added co-stimulatory signaling domains 4-1BB and CD28. When the transduced ROR-1 CAR-T cell comes into contact with its cognate receptor, a signal is transmitted by the CD3 zeta-chain, inducing lymphocyte proliferation and expression of trans-acting interleukins and chemokines that activate other immuno-reactive cells and in certain cases directly kill ROR1+ Cancer Stem Cells
Unmet Medical Need
Compelling evidence suggests that dormant cancer stem cells (CSCs) are considered the origin of therapeutic resistance, and are responsible for relapse and metastasis. We will selectively identify and attack CSCs through the ROR1 receptor, using CAR-T cells to address this unmet medical need.
Project Objective
Completion of a Pre-IND meeting
Major Proposed Activities
- Generate GMP-compatible ROR1 lentivirus with a single-chain variable fragment (scFv) with three signaling domains derived from CD3zeta, CD28 and 4-1BB
- Generate ROR1 CAR-T cells; complete studies of cell fate, persistence, efficacy and distribution in CLL, HNSCC, TNBC, ovarian, and pancreatic cancer
- Develop a ROR1 Companion Diagnostic test
Statement of Benefit to California:
Californians will benefit from this project in several significant ways. If the therapeutic is successful, it will extend the long-term survival rates for Californians with solid and hematologic tumors. Accomplishing the proposed studies will have an added economic benefit for California through creating and maintaining skilled jobs, and using resources from in-state companies. High cost hospital stays and treatments associated with advanced disease, will be significantly reduced.