TY - JOUR
T1 - Development and therapeutic manipulation of the head and neck cancer tumor environment to improve clinical outcomes
AU - Duhen, Thomas
AU - Gough, Michael J.
AU - Leidner, Rom S.
AU - Stanton, Sasha E.
N1 - Publisher Copyright:
Copyright © 2022 Duhen, Gough, Leidner and Stanton.
PY - 2022/7/22
Y1 - 2022/7/22
N2 - The clinical response to cancer therapies involves the complex interplay between the systemic, tumoral, and stromal immune response as well as the direct impact of treatments on cancer cells. Each individual's immunological and cancer histories are different, and their carcinogen exposures may differ. This means that even though two patients with oral tumors may carry an identical mutation in TP53, they are likely to have different pre-existing immune responses to their tumors. These differences may arise due to their distinct accessory mutations, genetic backgrounds, and may relate to clinical factors including previous chemotherapy exposure and concurrent medical comorbidities. In isolation, their cancer cells may respond similarly to cancer therapy, but due to their baseline variability in pre-existing immune responses, patients can have different responses to identical therapies. In this review we discuss how the immune environment of tumors develops, the critical immune cell populations in advanced cancers, and how immune interventions can manipulate the immune environment of patients with pre-malignancies or advanced cancers to improve therapeutic outcomes.
AB - The clinical response to cancer therapies involves the complex interplay between the systemic, tumoral, and stromal immune response as well as the direct impact of treatments on cancer cells. Each individual's immunological and cancer histories are different, and their carcinogen exposures may differ. This means that even though two patients with oral tumors may carry an identical mutation in TP53, they are likely to have different pre-existing immune responses to their tumors. These differences may arise due to their distinct accessory mutations, genetic backgrounds, and may relate to clinical factors including previous chemotherapy exposure and concurrent medical comorbidities. In isolation, their cancer cells may respond similarly to cancer therapy, but due to their baseline variability in pre-existing immune responses, patients can have different responses to identical therapies. In this review we discuss how the immune environment of tumors develops, the critical immune cell populations in advanced cancers, and how immune interventions can manipulate the immune environment of patients with pre-malignancies or advanced cancers to improve therapeutic outcomes.
KW - CD4
KW - CD8
KW - HNSCC (head and neck squamous cell carcinoma)
KW - OSCC (oral squamous cell carcinoma)
KW - TIL (tumor infiltrating lymphocytes)
KW - immunotherapy
KW - pre-malignancies
UR - http://www.scopus.com/inward/record.url?scp=85147975000&partnerID=8YFLogxK
U2 - 10.3389/froh.2022.902160
DO - 10.3389/froh.2022.902160
M3 - Review article
C2 - 35937775
AN - SCOPUS:85147975000
SN - 2673-4842
VL - 3
JO - Frontiers in Oral Health
JF - Frontiers in Oral Health
M1 - 902160
ER -