Monoclonal antibodies (mAbs) are widely used as targeted therapies for the treatment of human malignancies. However, despite the impressive responsiveness of certain types of cancers, resistance to many mAb therapies remains a serious clinical challenge for ovarian cancer, the most lethal gynecologic malignancy. A key activity of many therapeutic mAbs is their induction of antibody-dependent cell-mediated cytotoxicity (ADCC) by natural killer (NK) cells. Human NK cells exclusively recognize tumor bound antibodies by CD16a (Fc?RIIIa/FCGR3A), and its expression levels directly correlate with ADCC potency. CD16a expression and NK cell cytotoxic function, however, can undergo a marked down-regulation in cancer patients, including those with ovarian cancer. Thus, blocking CD16a down-regulation has clinical significance. CD16a down-regulation occurs by a proteolytic process upon NK cell activation by various stimuli (e.g., engagement of IgG, pro- inflammatory cytokines, and tumor cell interactions). We were the first to report that the membrane metalloprotease ADAM17 is expressed by NK cells and is the primary protease that cleaves CD16a. Moreover, we have determined the ADAM17 cleavage site in CD16a and have expressed a non-cleavable yet functional version of the receptor in NK cells. We hypothesize that blocking CD16a shedding in NK cells will augment their killing of ovarian cancer cells in the presence of therapeutic mAbs that induce ADCC. To test our hypothesis, we have devised distinct approaches to inhibit CD16a cleavage in primary human NK cells.
Our first Aim i s to genetically modify human pluripotent stem cells to derive NK cells that express non- cleavable CD16a or lack ADAM17 expression. These cells will be evaluated for their anti-tumor functionality by in vitro approaches.
Aim 2 is to evaluate the in vivo anti-ovarian cancer activity of NK cells engineered to block CD16a shedding. We will use a human xenograft model and ovarian cancer cell lines as well as primary tumor samples.
Aim 3 is to determine the in vivo anti-ovarian cancer activity of a selective ADAM17 inhibitor in combination with adoptively transferred human NK cells and therapeutic mAbs. The impact of our study is that it investigates CD16a shedding by NK cells as a pivotal mechanism of resistance to therapeutic mAbs in ovarian cancer patients.

Public Health Relevance

Ovarian cancer is the most lethal gynecologic malignancy and in contrast to many solid cancer types, the survival rate of women with epithelial ovarian cancer has changed little in the last 30 years. There is an urgent need for innovative therapeutic strategies, as most women with relapsed ovarian cancer will die of progressive disease. Various therapeutic antibodies have emerged as effective targeted therapies for the treatment of several human malignancies; however, this treatment has provided only limited responses in patients with advanced ovarian cancer. Studies described in our proposal offer a unique approach to bolster the efficacy of therapeutic antibodies. This study will be performed by a team of basic and physician-scientists that provides expertise in immunology, stem cell biology, genetic engineering, ovarian cancer clinical research, and immunotherapies.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA203348-03
Application #
9397530
Study Section
Cancer Immunopathology and Immunotherapy Study Section (CII)
Program Officer
Sommers, Connie L
Project Start
2016-01-01
Project End
2020-12-31
Budget Start
2018-01-01
Budget End
2018-12-31
Support Year
3
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Veterinary Sciences
Type
Schools of Veterinary Medicine
DUNS #
555917996
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
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Angelos, Mathew G; Ruh, Paige N; Webber, Beau R et al. (2017) Aryl hydrocarbon receptor inhibition promotes hematolymphoid development from human pluripotent stem cells. Blood 129:3428-3439
Ku, Amy W; Muhitch, Jason B; Powers, Colin A et al. (2016) Tumor-induced MDSC act via remote control to inhibit L-selectin-dependent adaptive immunity in lymph nodes. Elife 5: