Drug delivery for metabolism targeted cancer immunotherapy.

Taravat Khodaei, Sahil Inamdar, Abhirami P Suresh, Abhinav P Acharya
Author Information
  1. Taravat Khodaei: Biomedical Engineering, School of Biological and Health System Engineering, Arizona State University, Tempe, AZ 85281, USA.
  2. Sahil Inamdar: Chemical Engineering, School for Engineering of Matter, Transport, and Energy, Arizona State University, Tempe, AZ 85281, USA.
  3. Abhirami P Suresh: Biological Design, Arizona State University, Tempe, AZ 85281, USA.
  4. Abhinav P Acharya: Biomedical Engineering, School of Biological and Health System Engineering, Arizona State University, Tempe, AZ 85281, USA; Chemical Engineering, School for Engineering of Matter, Transport, and Energy, Arizona State University, Tempe, AZ 85281, USA; Biological Design, Arizona State University, Tempe, AZ 85281, USA; Materials Science and Engineering, School for Engineering of Matter, Transport, and Energy, Arizona State University, Tempe, AZ 85281, USA; Center for Immunotherapy, Vaccines and Virotherapy, Arizona State University, Tempe, AZ 85281, USA. Electronic address: abhi.acharya@asu.edu.

Abstract

Drug delivery vehicles have made a great impact on cancer immunotherapies in clinics and pre-clinical research. Notably, the science of delivery of cancer vaccines and immunotherapeutics, modulating immune cell functions has inspired development of several successful companies and clinical products. Interestingly, these drug delivery modalities not only modulate the function of immune cells (often quantified at the mRNA and protein levels), but also modulate the metabolism of these cells. Specifically, cancer immunotherapy often leads to activation of different immune cells such as dendritic cells, macrophages and T cells, which is driven by energy metabolism of these cells. Recently, there has been a great excitement about interventions that can directly modulate the energy metabolism of these immune cells and thus affect their function and in turn lead to a robust cancer immune response. Here we review few strategies that have been tested in clinic and pre-clinical research for generating effective metabolism-associated cancer therapies and immunotherapies.

Keywords

Grants

  1. R01 AI155907/NIAID NIH HHS
  2. R01 GM144966/NIGMS NIH HHS
  3. R01 AR078343/NIAMS NIH HHS

MeSH Term

Cancer Vaccines
Drug Delivery Systems
Humans
Immunotherapy
Neoplasms
T-Lymphocytes

Chemicals

Cancer Vaccines

Word Cloud

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