Review Article

Nanoengineered targeting strategy for cancer immunotherapy

Wei-min Yin1, Yu-wei Li1, Yun-qing Gu1, Min Luo1
1 Institute of Pediatrics, Children’s Hospital of Fudan University, and the Shanghai Key Laboratory of Medical Epigenetics, International Co-laboratory of Medical Epigenetics and Metabolism, Ministry of Science and Technology, Institutes of Biomedical Sciences, Fudan University, Shanghai 200032, China

Correspondence to: Min Luo: luo_min@fudan.edu.cn,
DOI: 10.1038/s41401-020-0417-3
Received: 12 December 2019
Accepted: 12 April 2020
Advance online: 12 May 2020

Abstract

Cancer immunotherapy is rapidly changing the paradigm of cancer care and treatment by evoking host immunity to kill cancer cells. As clinical approval of checkpoint inhibitors (e.g., ipilimumab and pembrolizumab) has been accelerated by a dramatic improvement of long-term survival in a small subset of patients compared to conventional chemotherapy, growing interesting research has focused on immunotherapy. However, majority of patients have not benefited from checkpoint therapies that only partially remove the inhibition of T cell functions. Insufficient systemic T cell responses, low immunogenicity and the immunosuppressive environment of tumors, create great challenges on therapeutic efficiency. Nanotechnology can integrate multiple functions within controlled size and shape, and has been explored as a unique avenue for the development of cancer immunotherapy. In this review, we mainly address how nanoengineered vaccines can induce robust T cell responses against tumors, as well as how nanomedicine can remodel the tumor immunosuppressive microenvironment to boost antitumor immune responses.
Keywords: cancer immunotherapy; nanomedicine; cancer vaccine; immune resistance; nanovaccine; immunosuppressive microenvironment

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