Combination therapy targeting both innate and adaptive immunity improves survival in a pre-clinical model of ovarian cancer

Journal for ImmunoTherapy of Cancer

Emily M. Cheney¹  Elizabeth A. Mittendorf¹  Jennifer L. Guerriero¹  Regina Bou Puerto²  Adrian Bertschi²  Christina A. Hartl²  Michael S. Goldberg²  Carolin Andresen² 

[1] Breast Tumor Immunology Laboratory, Susan F. Smith Center for Women’s Cancers, Dana-Farber Cancer Institute;Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute;

关键词: Ovarian cancer;    Cancer immunotherapy;    Combination therapy;    CD4+ T cells;    Innate immunity;   

DOI  :  10.1186/s40425-019-0654-5

来源: DOAJ

【 摘 要 】

Abstract Background Despite major advancements in immunotherapy among a number of solid tumors, response rates among ovarian cancer patients remain modest. Standard treatment for ovarian cancer is still surgery followed by taxane- and platinum-based chemotherapy. Thus, there is an urgent need to develop novel treatment options for clinical translation. Methods Our approach was to analyze the effects of standard chemotherapy in the tumor microenvironment of mice harboring orthotopic, syngeneic ID8-Vegf-Defb29 ovarian tumors in order to mechanistically determine a complementary immunotherapy combination. Specifically, we interrogated the molecular and cellular consequences of chemotherapy by analyzing gene expression and flow cytometry data. Results These data show that there is an immunosuppressive shift in the myeloid compartment, with increased expression of IL-10 and ARG1, but no activation of CD3+ T cells shortly after chemotherapy treatment. We therefore selected immunotherapies that target both the innate and adaptive arms of the immune system. Survival studies revealed that standard chemotherapy was complemented most effectively by a combination of anti-IL-10, 2′3’-cGAMP, and anti-PD-L1. Immunotherapy dramatically decreased the immunosuppressive myeloid population while chemotherapy effectively activated dendritic cells. Together, combination treatment increased the number of activated T and dendritic cells as well as expression of cytotoxic factors. It was also determined that the immunotherapy had to be administered concurrently with the chemotherapy to reverse the acute immunosuppression caused by chemotherapy. Mechanistic studies revealed that antitumor immunity in this context was driven by CD4+ T cells, which acquired a highly activated phenotype. Our data suggest that these CD4+ T cells can kill cancer cells directly via granzyme B-mediated cytotoxicity. Finally, we showed that this combination therapy is also effective at delaying tumor growth substantially in an aggressive model of lung cancer, which is also treated clinically with taxane- and platinum-based chemotherapy. Conclusions This work highlights the importance of CD4+ T cells in tumor immunology. Furthermore, the data support the initiation of clinical trials in ovarian cancer that target both innate and adaptive immunity, with a focus on optimizing dosing schedules.

【 授权许可】

Unknown