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Methods for Studying Tumor-immune Interactions and Response to Immunotherapies

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Pilar de la Puente

Pilar de la Puente

University of South Dakota Sanford School of Medicine; Sanford Research

Dr. De la Puente received her PhD at the University of Salamanca in Spain in the field of Biomedical Engineering and Biological Sciences. The scope of her studies included development of novel, autologous cell cultures in a biocompatible matrix enriched with growth factors for tissue engineering applications. She focused on the recreation of the tumor microenvironment of hematological malignancies during her postdoctoral fellowship at Washington University in St. Louis School of Medicine. Currently, Dr. De la Puente is an Assistant Professor at Sanford Research/ University of South Dakota Sanford School of Medicine where she studies the role of the tumor microenvironment in cancer progression, drug resistance, and cancer immunology. Her lab is developing 3D models of the tumor microenvironment in order to more accurately mimic cell-cell and cell-matrix interactions for personalized medicine. She was recently awarded the prestigious Young Investigator Lush Prize, and she is an active entrepreneur with several patents and roles in start-up companies.

Collection Overview

A key hallmark of tumors is the cancer cell's ability to keep the host’s immune system at bay. These evasion mechanisms involve not only the expression of immunosuppressive surface proteins by the tumor cells themselves but also the complex microenvironment of the tumors, including the immunosuppressive cytokines that are released by the cancer cells. An increased understanding of tumor immune surveillance has led to immunotherapy emerging as a promising treatment strategy for several types of cancer tumors. To better understand the role of the tumor microenvironment on variations of cancer immune evasion, it is necessary to account for the tumor-immune interactions and cytokines originating from the tumor and from microenvironment interactions. In response to such barriers, several methods for studying tumor-immune interactions and response to immunotherapies are crucially required.

Examples of methods to be included in this collection are: spheroids, organoids, hydrogels, 3D scaffolds, 3D bio-printing, and microfluidics attempting the recreation of certain aspects of the immunosuppressive tumor microenvironment, tumor-immune interactions and their influence on immunotherapies’ responses. Of particular interest are models taking into account patient heterogeneity in a precision-based manner and models recapitulating key physiologically relevant components of the tumor microenvironment.

Articles

Purification and Expansion of Mouse Invariant Natural Killer T Cells for in vitro and in vivo Studies
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Purification and Expansion of Mouse Invariant Natural Killer T Cells for in vitro and in vivo Studies

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Cited by 5

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2021

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