Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2024 Jan 12;31:5. doi: 10.1186/s12929-024-00998-8

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

PMC Copyright notice

Fig. 2 — Engineering strategies to overcome immune evasion. Innovative engineering strategies have been deployed to substantially enhance the recognition of tumors, the durability of therapeutic cells, their ability to infiltrate the tumor microenvironment, and the overall effectiveness of cellular therapies. These strategies encompass a range of techniques, including the incorporation of multiple targeting mechanisms (A), fortifying therapeutic cells with cytokines (B), modifying the immunosuppressive tumor microenvironment (C), amplifying cell infiltration capabilities (D), and employing combination therapies (E). TanCAR, tandem CAR; iNKT, invariant natural killer T; MAIT, mucosal associated invariant T; γδ T, gamma delta T; ICB, immune checkpoint inhibitor; ECM, extracellular matrix