Abstract
Pancreatic cancer is known to be highly aggressive, and desmoplasia-induced accumulation of extracellular matrix (ECM), which is a hallmark of many pancreatic cancers, severely restricts the therapeutic efficacy of both immunotherapeutics and conventional chemotherapeutics due to the ECM functioning as a major physical barrier against permeation and penetration. In the case of cell-based immunotherapeutics, there are several other bottlenecks preventing translation into clinical use due to their biological nature; for example, poor availability of cell therapeutic in a readily usable form due to difficulties in production, handling, shipping, and storage. To address these challenges, we have isolated allogeneic natural killer (NK) cells from healthy donors and expanded them in vitro to generate cryopreserved stocks. These cryopreserved NK cells were thawed to evaluate their therapeutic efficacy against desmoplastic pancreatic tumors, ultimately aiming to develop a readily accessible and mass-producible off-the-shelf cell-based immunotherapeutic. The cultured NK cells post-thawing retained highly pure populations of activated NK cells that expressed various activating receptors and a chemokine receptor. Furthermore, systemic administration of NK cells induced greater in vivo tumor growth suppression when compared with gemcitabine, which is the standard chemotherapeutic used for pancreatic cancer treatment. The potent antitumor effect of NK cells was mediated by efficient tumor-homing ability and infiltration into desmoplastic tumor tissues. Moreover, the infiltration of NK cells led to strong induction of apoptosis, elevated expression of the antitumor cytokine interferon (IFN)-γ, and inhibited expression of the immunosuppressive transforming growth factor (TGF)-β in tumor tissues. Expanded and cryopreserved NK cells are strong candidates for future cell-mediated systemic immunotherapy against pancreatic cancer.
Highlights
Pancreatic cancer is the fifth leading cause of death from cancer in the world, and the 5-year survival rate is a dismal 6% in Europe and the United States [1,2,3]
Because of these limitations of conventional treatment methods, various immunotherapeutics, such as immune checkpoint inhibitors, cancer vaccines, or chimeric antigen receptor T cells [7], are currently being evaluated in clinical trials for the treatment of pancreatic cancer [8]. This direction has been taken in part because of the observation that higher levels of immune cells, such as natural killer (NK) cells, in circulation are associated with improved survival of pancreatic cancer patients, suggesting that boosting of host antitumor immunity by therapeutics may lead to better disease management [9,10,11,12]
The NK cell-mediated killing of both MIA PaCa-2 and gradually increased from 48 h to 96 h post treatment. These results indicate that NK cells can elicit
Summary
Pancreatic cancer is the fifth leading cause of death from cancer in the world, and the 5-year survival rate is a dismal 6% in Europe and the United States [1,2,3]. Overall survival benefits provided by either gemcitabine-based therapy are limited by the highly desmoplastic nature of pancreatic cancer, which prohibits drug penetration and dispersion into tumor tissues. Because of these limitations of conventional treatment methods, various immunotherapeutics, such as immune checkpoint inhibitors, cancer vaccines, or chimeric antigen receptor T cells [7], are currently being evaluated in clinical trials for the treatment of pancreatic cancer [8]. This direction has been taken in part because of the observation that higher levels of immune cells, such as natural killer (NK) cells, in circulation are associated with improved survival of pancreatic cancer patients, suggesting that boosting of host antitumor immunity by therapeutics may lead to better disease management [9,10,11,12]
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