Adoptively transferred ex vivo expanded gamma delta-T cells mediate in vivo antitumor activity in preclinical mouse models of breast cancer

作者：Beck Benjamin H; Kim Hyung Gyoon; Kim Hyunki; Samuel Sharon; Liu Zhiyong; Shrestha Robin; Haines Hilary; Zinn Kurt; Lopez Richard D^*

来源：Breast Cancer Research and Treatment, 2010, 122(1): 135-144.

DOI：10.1007/s10549-009-0527-6

• gamma delta-T cells
• Immunotherapy
• Cell therapy
• Innate immunity

In contrast to antigen-specific alpha beta-T cells (adaptive immune system), gamma delta-T cells can recognize and lyse malignantly transformed cells almost immediately upon encounter in a manner that does not require the recognition of tumor-specific antigens (innate immune system). Given the well-documented capacity of gamma delta-T cells to innately kill a variety of malignant cells, efforts are now actively underway to exploit the antitumor properties of gamma delta-T cells for clinical purposes. Here, we present for the first time preclinical in vivo mouse models of gamma delta-T cell-based immunotherapy directed against breast cancer. These studies were explicitly designed to approximate clinical situations in which adoptively transferred gamma delta-T cells would be employed therapeutically against breast cancer. Using radioisotope-labeled gamma delta-T cells, we first show that adoptively transferred gamma delta-T cells localize to breast tumors in a mouse model (4T1 mammary adenocarcinoma) of human breast cancer. Moreover, by using an antibody directed against the gamma delta-T cell receptor (TCR), we determined that localization of adoptively transferred gamma delta-T cells to tumor is a TCR-dependant process. Additionally, biodistribution studies revealed that adoptively transferred gamma delta-T cells traffic differently in tumor-bearing mice compared to healthy mice with fewer gamma delta-T cells localizing into the spleens of tumor-bearing mice. Finally, in both syngeneic (4T1) and xenogeneic (2Lmp) models of breast cancer, we demonstrate that adoptively transferred gamma delta-T cells are both effective against breast cancer and are otherwise well-tolerated by treated animals. These findings provide a strong preclinical rationale for using ex vivo expanded adoptively transferred gamma delta-T cells as a form of cell-based immunotherapy for the treatment of breast cancer. Additionally, these studies establish that clinically applicable methods for radiolabeling gamma delta-T cells allows for the tracking of adoptively transferred gamma delta-T cells in tumor-bearing hosts.

• 出版日期2010-7