Assessment of Immune Cell Populations in Tumor Tissue and Peripheral Blood Samples from Head and Neck Squamous Cell Carcinoma Patients
Author(s) -
Ana Căruntu,
Liliana Moraru,
Mihaela Surcel,
Adriana Munteanu,
Cristiana Tănase,
Carolina Constantin,
Sabina Zurac,
Constantin Căruntu,
Monica Neagu
Publication year - 2021
Publication title -
analytical cellular pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.576
H-Index - 24
eISSN - 2210-7185
pISSN - 2210-7177
DOI - 10.1155/2021/2328218
Subject(s) - immune system , head and neck squamous cell carcinoma , tumor microenvironment , cd8 , lymphocyte , biology , cancer , cytotoxic t cell , immunology , cell , cancer research , pathology , medicine , head and neck cancer , biochemistry , genetics , in vitro
Head and neck squamous cell carcinoma (HNSCC) is a common type of cancer worldwide. Strong connections have been revealed between immune cells and the pathogenesis of HNSCC. Important differences regarding the levels of immune cell subpopulations in both peripheral circulation and tumor microenvironment were emphasized, with some of them having prognostic significance. In our study, we performed an analysis of immune changes in the tumor tissue and the peripheral blood of untreated HNSCC patients, investigating the proportions of different immune cell populations in these two compartments. The local infiltrating lymphocytes were mainly cytotoxic T cells (CD8 + ). We have also revealed an increased level of B lymphocytes (CD19 + ) in the tumor microenvironment. In peripheral blood, the most important lymphocyte subtype was represented by the helper T lymphocytes (CD4 + ). We also found an increased proportion of circulating NK cells (CD56 + ). Our results showed significant differences between all investigated lymphocyte subtypes in the peripheral blood and the tumor tissue of untreated HNSCC patients, suggesting that the local and systemic expressions of antitumor immune responses are different and that investigation of immune cell proportions in peripheral circulation has different cues that do not reflect the immune infiltrate pattern within the tumor microenvironment. Further studies are necessary to unveil the complex interplay involving local and systemic events in the immune system's fight against cancer.
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