Engineering strategies to optimise adoptive cell therapy in ovarian cancer.


Journal

Cancer treatment reviews
ISSN: 1532-1967
Titre abrégé: Cancer Treat Rev
Pays: Netherlands
ID NLM: 7502030

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 08 08 2023
revised: 01 10 2023
accepted: 03 10 2023
medline: 27 11 2023
pubmed: 15 10 2023
entrez: 14 10 2023
Statut: ppublish

Résumé

Ovarian cancer is amongst the ten most common cancer types in women, and it is one of the leading causes of death. Despite the promising results of targeted therapies, including anti-angiogenic agents and poly (ADP-ribose) polymerase inhibitors (PARPi), the majority of patients will relapse and develop treatment resistance, implying that novel therapeutic strategies are required. Adoptive cell therapy (ACT) refers to the process by which autologous immune cells are used to eliminate cancer. Examples include tumour infiltrating lymphocytes (TILs), T cells genetically engineered with T cell receptors (TCR), or chimeric antigen receptor (CAR)-T cells. Recently, ACT has revealed promising results in the treatment of haematological malignancies, however, its application to solid tumours is still limited due to lack of functionality and persistence of T cells, prevalence of an exhausted phenotype and impaired trafficking towards the tumour microenvironment (TME). In this review we explore the potential of ACT for the treatment of ovarian cancer and strategies to overcome its principal limitations.

Identifiants

pubmed: 37837788
pii: S0305-7372(23)00125-1
doi: 10.1016/j.ctrv.2023.102632
pii:
doi:

Substances chimiques

Receptors, Antigen, T-Cell 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

102632

Informations de copyright

Copyright © 2023. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: CG – no declarations. MK, GK and RH are employees of Instil Bio with stock or stock options. RJE – received honoraria from GSK, & Clovis Inc.

Auteurs

Catarina Guerra (C)

InstilBio UK, 48 Grafton St, Manchester M13 9XX, Manchester, United Kingdom; School of Medical Sciences, The University of Manchester, Oxford Rd, Manchester, United Kingdom. Electronic address: catarina.guerra@postgrad.manchester.ac.uk.

Milena Kalaitsidou (M)

InstilBio UK, 48 Grafton St, Manchester M13 9XX, Manchester, United Kingdom. Electronic address: milena.kalaitsidou@instilbio.com.

Gray Kueberuwa (G)

InstilBio UK, 48 Grafton St, Manchester M13 9XX, Manchester, United Kingdom. Electronic address: gray.kueberuwa@instilbio.com.

Robert Hawkins (R)

InstilBio UK, 48 Grafton St, Manchester M13 9XX, Manchester, United Kingdom. Electronic address: robert.hawkins@instilbio.com.

Richard Edmondson (R)

School of Medical Sciences, The University of Manchester, Oxford Rd, Manchester, United Kingdom. Electronic address: richard.edmondson@manchester.ac.uk.

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Classifications MeSH