| Literature DB >> 34844835 |
Abstract
Currently, medicine lacks the ability to reprogram selected immune cells so they possess all the functions which, from a clinical standpoint, physicians might wish them to have. To solve this problem, scientists have been marrying concepts from materials science, immunology, and genetic engineering to develop novel nanotherapeutics that directly genetically reprogram immune cells inside the body. These products could address key limitations of existing ex vivo-engineered cell immunotherapies and substantially enhance patient access and outcomes. This review highlights the latest advances in this rapidly emerging biotech field and discusses challenges in translating these preclinical studies into successful clinical nanomedicines.Entities:
Keywords: CAR T-cell; Dendritic cell; In vivo cell reprogramming; Macrophage; Nanotechnology; Nonviral gene therapy; T-cell therapy
Mesh:
Year: 2021 PMID: 34844835 PMCID: PMC8792224 DOI: 10.1016/j.smim.2021.101537
Source DB: PubMed Journal: Semin Immunol ISSN: 1044-5323 Impact factor: 11.130