Abstract |
IFN-α receptor (IFNAR) is critical for maintaining the crosstalk between cancer cells and lymphocytes. We investigated IFNAR1 expression in peripheral blood CD4+ and CD8+ T cells and explored their relationships with plasma cytokines, chemosensitivity and infiltrated T cells in the tumor microenvironment (TME) of colorectal cancer (CRC). The levels of IFNAR1, IFN-γ, and PD1 in peripheral T cells were tested using flow cytometry. Immunohistochemical staining of IFNAR1 in CRC tissues was performed. A cytometric bead array was used to determine the plasma concentrations of cytokines. In CRC patients, IFNAR1 levels were significantly increased in peripheral blood T cells, and plasma IL-6 levels were also significantly increased. Pearson correlation analysis revealed that IFNAR1 expression in CD8+ T cells was negatively associated with plasma IL-2, IFN-γ, and TNFα. IFNAR1 expression in CD4+ T cells was positively associated with TME infiltrated levels of CD8+ T cells. The levels of CD8+ T cells with IFNAR1 and plasma IFN-γ were associated with chemosensitivity. Collectively, IFNAR1 levels in CD4+ and CD8+ T cells were significantly upregulated in CRC patients and positively associated with T-cell infiltration. IFNAR1 may be a chemotherapy biomarker for predicting response.
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Authors | Lei Yang, Xiaojing Zhang, Xiaoxi Huang, Xichen Dong, Shui Jing, Yudong Zhang, Baocheng Zhao, Zhenjun Wang, Hao Qu |
Journal | Cytokine
(Cytokine)
Vol. 159
Pg. 156008
(11 2022)
ISSN: 1096-0023 [Electronic] England |
PMID | 36063748
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved. |
Chemical References |
- Cytokines
- IFNAR1 protein, human
- Interleukin-2
- Interleukin-6
- Tumor Necrosis Factor-alpha
- Receptor, Interferon alpha-beta
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Topics |
- CD4-Positive T-Lymphocytes
(metabolism)
- CD8-Positive T-Lymphocytes
(metabolism)
- Colorectal Neoplasms
(metabolism)
- Cytokines
(metabolism)
- Humans
- Interleukin-2
(metabolism)
- Interleukin-6
(metabolism)
- Lymphocytes, Tumor-Infiltrating
- Receptor, Interferon alpha-beta
(metabolism)
- Tumor Microenvironment
- Tumor Necrosis Factor-alpha
(metabolism)
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