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
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
19 April 2023
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).
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.
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fimmu-14-1176724 (1)
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fimmu-14-1176724
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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
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Date deposited: 06 Jun 2023 17:14
Last modified: 27 Mar 2024 02:51
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Author:
Alex Look
Author:
Daniel Burns
Corporate Author: et al.
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