The University of Southampton
University of Southampton Institutional Repository

Towards a better understanding of human iNKT cell subpopulations for improved clinical outcomes

Towards a better understanding of human iNKT cell subpopulations for improved clinical outcomes
Towards a better understanding of human iNKT cell subpopulations for improved clinical outcomes

Invariant natural killer T (iNKT) cells are a unique T lymphocyte population expressing semi-invariant T cell receptors (TCRs) that recognise lipid antigens presented by CD1d. iNKT cells exhibit potent anti-tumour activity through direct killing mechanisms and indirectly through triggering the activation of other anti-tumour immune cells. Because of their ability to induce potent anti-tumour responses, particularly when activated by the strong iNKT agonist αGalCer, they have been the subject of intense research to harness iNKT cell-targeted immunotherapies for cancer treatment. However, despite potent anti-tumour efficacy in pre-clinical models, the translation of iNKT cell immunotherapy into human cancer patients has been less successful. This review provides an overview of iNKT cell biology and why they are of interest within the context of cancer immunology. We focus on the iNKT anti-tumour response, the seminal studies that first reported iNKT cytotoxicity, their anti-tumour mechanisms, and the various described subsets within the iNKT cell repertoire. Finally, we discuss several barriers to the successful utilisation of iNKT cells in human cancer immunotherapy, what is required for a better understanding of human iNKT cells, and the future perspectives facilitating their exploitation for improved clinical outcomes.

CD1d, cancer, iNKT cell, immunotharapy, lipid
1664-3224
Look, Alex
5229d2c0-2e0a-4c94-8fd4-443c04d3133e
Burns, Daniel
40b9dc88-a54a-4365-b747-4456d9203146
Tews, Ivo
9117fc5e-d01c-4f8d-a734-5b14d3eee8dd
Roghanian, Ali
e2b032c2-60a0-4522-a3d8-56a768792f36
Mansour, Salah
4aecba5a-8387-4f7b-b766-0a9c309ccb8b
et al.
Look, Alex
5229d2c0-2e0a-4c94-8fd4-443c04d3133e
Burns, Daniel
40b9dc88-a54a-4365-b747-4456d9203146
Tews, Ivo
9117fc5e-d01c-4f8d-a734-5b14d3eee8dd
Roghanian, Ali
e2b032c2-60a0-4522-a3d8-56a768792f36
Mansour, Salah
4aecba5a-8387-4f7b-b766-0a9c309ccb8b

Look, Alex, Burns, Daniel and Tews, Ivo , et al. (2023) Towards a better understanding of human iNKT cell subpopulations for improved clinical outcomes. Frontiers in Immunology, 14, [1176724]. (doi:10.3389/fimmu.2023.1176724).

Record type: Review

Abstract

Invariant natural killer T (iNKT) cells are a unique T lymphocyte population expressing semi-invariant T cell receptors (TCRs) that recognise lipid antigens presented by CD1d. iNKT cells exhibit potent anti-tumour activity through direct killing mechanisms and indirectly through triggering the activation of other anti-tumour immune cells. Because of their ability to induce potent anti-tumour responses, particularly when activated by the strong iNKT agonist αGalCer, they have been the subject of intense research to harness iNKT cell-targeted immunotherapies for cancer treatment. However, despite potent anti-tumour efficacy in pre-clinical models, the translation of iNKT cell immunotherapy into human cancer patients has been less successful. This review provides an overview of iNKT cell biology and why they are of interest within the context of cancer immunology. We focus on the iNKT anti-tumour response, the seminal studies that first reported iNKT cytotoxicity, their anti-tumour mechanisms, and the various described subsets within the iNKT cell repertoire. Finally, we discuss several barriers to the successful utilisation of iNKT cells in human cancer immunotherapy, what is required for a better understanding of human iNKT cells, and the future perspectives facilitating their exploitation for improved clinical outcomes.

Text
fimmu-14-1176724 (1) - Accepted Manuscript
Available under License Creative Commons Attribution.
Download (2MB)
Text
fimmu-14-1176724 - Version of Record
Available under License Creative Commons Attribution.
Download (2MB)

More information

Accepted/In Press date: 4 April 2023
Published date: 19 April 2023
Keywords: CD1d, cancer, iNKT cell, immunotharapy, lipid

Identifiers

Local EPrints ID: 477471
URI: http://eprints.soton.ac.uk/id/eprint/477471
ISSN: 1664-3224
PURE UUID: e85b928b-2bfb-4625-8a90-464b3a18b873
ORCID for Daniel Burns: ORCID iD orcid.org/0000-0001-6976-1068
ORCID for Ivo Tews: ORCID iD orcid.org/0000-0002-4704-1139
ORCID for Ali Roghanian: ORCID iD orcid.org/0000-0003-1316-4218
ORCID for Salah Mansour: ORCID iD orcid.org/0000-0002-5982-734X

Catalogue record

Date deposited: 06 Jun 2023 17:14
Last modified: 27 Mar 2024 02:51

Export record

Altmetrics

Contributors

Author: Alex Look
Author: Daniel Burns ORCID iD
Author: Ivo Tews ORCID iD
Author: Ali Roghanian ORCID iD
Author: Salah Mansour ORCID iD
Corporate Author: et al.

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×