Accession Number:

ADA595624

Title:

Adoptive Immunotherapy for Epithelial Ovarian Cancer Using T-cells Simultaneously Targeted to Tumor and Tumor-Associated Macrophages

Descriptive Note:

Addensum to final rept. 15 Jun 2012-30 Nov 2013

Corporate Author:

KINGS COLL LONDON (UNITED KINGDOM)

Personal Author(s):

Report Date:

2013-12-01

Pagination or Media Count:

17.0

Abstract:

Our initial hypothesis was that chimeric antigen receptor CAR-based immunotherapy of epithelial ovarian carcinoma EOC could be potentiated by depletion of tumor-associated macrophages TAM. To test this, we engineered T-cells to express CARs with specificity for MUC1 expressed by tumor cells and CSF-1R expressed both by tumor cells and TAM. In-vitro experiments demonstrated some efficacy of this approach but significant anti-tumor activity could not be confirmed in-vivo. Consequently, a revised statement of work was agreed in which CAR-mediated targeting of ErbB receptors by EOC tumor cells was pursued instead. A CAR termed T1E28z was engineered which engages several ErbB receptor dimers that are upregulated in EOC. Liposomal clodronate was used to achieve depletion of TAM. T1E28z-transduced T-cells proved effective in killing both autologus patient-derived tumor cell cultures and EOC cell lines IGROV-1 and SKOV-3 in-vitro. Using bioluminescence imaging BLI, we then demonstrated that T1E28z T-cells mediated the regression of established intraperitoneal SKOV-luc tumors in SCID Beige mice. Highly efficient depletion of TAM was achieved using liposomal clodronate. However, this did not influence anti-tumor activity and appeared to reduced efficacy somewhat. To monitor Tcell persistence in this model, renilla luciferase was co-expressed in T1E28z T-cells. This analysis revealed that T-cells undergo progressive decline in tumor-bearing mice, providing a rationale for repeated T-cell administration. In support of this, we found that dual dosing with T1E28z T-cells enhanced therapeutic efficacy in this model. Bridging the gap to clinical implementation, proof of concept was also demonstrated for the use of the human sodium iodide symporter hNIS as a clinically applicable imaging reporter of T-cell location. We provide evidence that administration of 99mTc-pertechnetate enables the serial real-time tracking of T1E28zhNIS T-cells in-vivo, using SPECT-CT.

Subject Categories:

  • Medicine and Medical Research

Distribution Statement:

APPROVED FOR PUBLIC RELEASE