Recent clinical success of immune checkpoint inhibitors and chimeric antigen receptor T cells has highly increased the attention for the field of immunotherapy. However, identifying responders to these therapies is challenging, underscoring the necessity for translational models that increase understanding of tumor-immune responses.
In the present study, a co-culture system containing immune cells and vasculature was established. Both are essential components of the tumor microenvironment and are very often lacking in in vitro tumor models, highlighting the added value of our co-culture platform. We focused on optimizing endothelial and CD8+ T cell co-cultures and subsequently assessing T cell migration from the endothelial tubes via endothelial sprouts towards various . In order to generate stratified 3D co-cultures, the OrganoPlate® Graft containing 64 microfluidic culture units was used. Generated sprouts were stable and perfusable. The central chamber is designed for culturing complex microtissues such as spheroids, organoids and explants. CD8+ T cell migration was observed both via the sprouts as well as by crossing the endothelial barrier, and increased in presence of gradients of CCL2, CCXl12 and CCL9.
We here present a high throughput co-culture system containing angiogenic endothelial tubules and CD8+ T cells. These co-cultures are highly suitable for studying T cell migration, which precedes the detection and recognition of antigens at the surface of antigen-presenting cells and for interactions with other cells involved in the immune response. In addition, these co-cultures serve as a platform for understanding the interplay between T cell migration and angiogenesis in the tumor microenvironment. Furthermore, we envision that this model will evolve into an immunocompetent patient-derived tumor model that can be used to study immune responses to tumors.
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