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Intratumoral CD45+CD71+ erythroid cells induce immune tolerance and predict tumor recurrence in hepatocellular carcinoma

CD45+CD71+ erythroid cells generated through splenic extramedullary erythropoiesis have recently been found to suppress anti-infection and tumor immunity in neonates and adults with malignances. However, their role in tumor microenvironment has not been investigated. In the present study, we found t...

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Published in:Cancer letters 2021-02, Vol.499, p.85-98
Main Authors: Chen, Jie, Qiao, Yi-Dan, Li, Xing, Xu, Jian-Liang, Ye, Qing-Jian, Jiang, Nan, Zhang, Hui, Wu, Xiang-Yuan
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cited_by cdi_FETCH-LOGICAL-c320t-9e85b64bc05ff75c3de0d5fbc99e7f005a06653066c43b0eb5b80c43170079193
cites cdi_FETCH-LOGICAL-c320t-9e85b64bc05ff75c3de0d5fbc99e7f005a06653066c43b0eb5b80c43170079193
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container_title Cancer letters
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Wu, Xiang-Yuan
description CD45+CD71+ erythroid cells generated through splenic extramedullary erythropoiesis have recently been found to suppress anti-infection and tumor immunity in neonates and adults with malignances. However, their role in tumor microenvironment has not been investigated. In the present study, we found that the number of CD45+CD71+ erythroid cells was significantly elevated in hepatocellular carcinoma (HCC) tissues compared to that in paratumor region and circulation. Additionally, they were more abundant in HCC tissues compared to some immune suppressive cells as well as CD45−CD71+ erythroid cells. CD45+CD71+ erythroid cells suppressed T cells through generation of reactive oxygen species, IL-10, and TGF-β in a paracrine and cell-cell contact manner, and their suppressive effect was stronger than that of myeloid-derived suppressor cells. The abundance of CD45+CD71+ erythroid cells in tumor tissue, as illustrated via immunofluorescence, predicted disease-free survival and overall survival, and its prognostic value was better than that of Cancer of the Liver Italian Program score. This study demonstrated that accumulation of intratumoral CD45+CD71+ erythroid cells in HCC tissues could play a superior immunosuppressive role in tumor microenvironment and may serve as a valuable biomarker to predict recurrence of HCC. •CD45+CD71+ erythroid cells were enriched in Chronic Hepatitis B (CHB) and hepatocellular carcinoma (HCC) tissues.•These cells suppressed T cells (both CD4+ and CD8+) by generation of ROS, IL-10, and TGF-β.•The abundance of these cells in tumor tissue predicted tumor recurrence of HCC.
doi_str_mv 10.1016/j.canlet.2020.12.003
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However, their role in tumor microenvironment has not been investigated. In the present study, we found that the number of CD45+CD71+ erythroid cells was significantly elevated in hepatocellular carcinoma (HCC) tissues compared to that in paratumor region and circulation. Additionally, they were more abundant in HCC tissues compared to some immune suppressive cells as well as CD45−CD71+ erythroid cells. CD45+CD71+ erythroid cells suppressed T cells through generation of reactive oxygen species, IL-10, and TGF-β in a paracrine and cell-cell contact manner, and their suppressive effect was stronger than that of myeloid-derived suppressor cells. The abundance of CD45+CD71+ erythroid cells in tumor tissue, as illustrated via immunofluorescence, predicted disease-free survival and overall survival, and its prognostic value was better than that of Cancer of the Liver Italian Program score. This study demonstrated that accumulation of intratumoral CD45+CD71+ erythroid cells in HCC tissues could play a superior immunosuppressive role in tumor microenvironment and may serve as a valuable biomarker to predict recurrence of HCC. •CD45+CD71+ erythroid cells were enriched in Chronic Hepatitis B (CHB) and hepatocellular carcinoma (HCC) tissues.•These cells suppressed T cells (both CD4+ and CD8+) by generation of ROS, IL-10, and TGF-β.•The abundance of these cells in tumor tissue predicted tumor recurrence of HCC.</description><identifier>ISSN: 0304-3835</identifier><identifier>EISSN: 1872-7980</identifier><identifier>DOI: 10.1016/j.canlet.2020.12.003</identifier><identifier>PMID: 33279623</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>Adult ; Aged ; Antibodies ; Antigens ; Antigens, CD - metabolism ; Carcinoma, Hepatocellular - immunology ; Carcinoma, Hepatocellular - mortality ; Carcinoma, Hepatocellular - therapy ; Carcinoma, Hepatocellular - virology ; CD45 antigen ; Cell adhesion ; Cell growth ; Cells, Cultured ; Coculture Techniques ; Disease-Free Survival ; Erythroid cells ; Erythroid Cells - immunology ; Erythroid Cells - metabolism ; Erythropoiesis ; Female ; Flow cytometry ; Follow-Up Studies ; Hematopoiesis, Extramedullary - immunology ; Hepatectomy ; Hepatitis B ; Hepatitis B, Chronic - immunology ; Hepatitis B, Chronic - pathology ; Hepatitis B, Chronic - virology ; Hepatocellular carcinoma ; Humans ; Immune tolerance ; Immunofluorescence ; Immunological tolerance ; Infections ; Interleukin 10 ; Investigations ; Italy - epidemiology ; Kaplan-Meier Estimate ; Leukocyte Common Antigens - metabolism ; Liver - immunology ; Liver - pathology ; Liver - surgery ; Liver - virology ; Liver cancer ; Liver Neoplasms - immunology ; Liver Neoplasms - mortality ; Liver Neoplasms - virology ; Lymphocytes ; Lymphocytes T ; Male ; Medical prognosis ; Middle Aged ; Neonates ; Neoplasm Recurrence, Local - epidemiology ; Neoplasm Recurrence, Local - immunology ; Neoplasm Recurrence, Local - pathology ; Paracrine signalling ; Primary Cell Culture ; Prognosis ; Reactive oxygen species ; Receptors, Transferrin - metabolism ; Retrospective Studies ; Risk Assessment - methods ; Spleen ; Suppressor cells ; T cell receptors ; T-Lymphocytes - immunology ; Tumor Escape ; Tumor Microenvironment - immunology ; Young Adult</subject><ispartof>Cancer letters, 2021-02, Vol.499, p.85-98</ispartof><rights>2020</rights><rights>Copyright © 2020. 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However, their role in tumor microenvironment has not been investigated. In the present study, we found that the number of CD45+CD71+ erythroid cells was significantly elevated in hepatocellular carcinoma (HCC) tissues compared to that in paratumor region and circulation. Additionally, they were more abundant in HCC tissues compared to some immune suppressive cells as well as CD45−CD71+ erythroid cells. CD45+CD71+ erythroid cells suppressed T cells through generation of reactive oxygen species, IL-10, and TGF-β in a paracrine and cell-cell contact manner, and their suppressive effect was stronger than that of myeloid-derived suppressor cells. The abundance of CD45+CD71+ erythroid cells in tumor tissue, as illustrated via immunofluorescence, predicted disease-free survival and overall survival, and its prognostic value was better than that of Cancer of the Liver Italian Program score. 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However, their role in tumor microenvironment has not been investigated. In the present study, we found that the number of CD45+CD71+ erythroid cells was significantly elevated in hepatocellular carcinoma (HCC) tissues compared to that in paratumor region and circulation. Additionally, they were more abundant in HCC tissues compared to some immune suppressive cells as well as CD45−CD71+ erythroid cells. CD45+CD71+ erythroid cells suppressed T cells through generation of reactive oxygen species, IL-10, and TGF-β in a paracrine and cell-cell contact manner, and their suppressive effect was stronger than that of myeloid-derived suppressor cells. The abundance of CD45+CD71+ erythroid cells in tumor tissue, as illustrated via immunofluorescence, predicted disease-free survival and overall survival, and its prognostic value was better than that of Cancer of the Liver Italian Program score. This study demonstrated that accumulation of intratumoral CD45+CD71+ erythroid cells in HCC tissues could play a superior immunosuppressive role in tumor microenvironment and may serve as a valuable biomarker to predict recurrence of HCC. •CD45+CD71+ erythroid cells were enriched in Chronic Hepatitis B (CHB) and hepatocellular carcinoma (HCC) tissues.•These cells suppressed T cells (both CD4+ and CD8+) by generation of ROS, IL-10, and TGF-β.•The abundance of these cells in tumor tissue predicted tumor recurrence of HCC.</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>33279623</pmid><doi>10.1016/j.canlet.2020.12.003</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0001-8237-6113</orcidid></addata></record>
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subjects Adult
Aged
Antibodies
Antigens
Antigens, CD - metabolism
Carcinoma, Hepatocellular - immunology
Carcinoma, Hepatocellular - mortality
Carcinoma, Hepatocellular - therapy
Carcinoma, Hepatocellular - virology
CD45 antigen
Cell adhesion
Cell growth
Cells, Cultured
Coculture Techniques
Disease-Free Survival
Erythroid cells
Erythroid Cells - immunology
Erythroid Cells - metabolism
Erythropoiesis
Female
Flow cytometry
Follow-Up Studies
Hematopoiesis, Extramedullary - immunology
Hepatectomy
Hepatitis B
Hepatitis B, Chronic - immunology
Hepatitis B, Chronic - pathology
Hepatitis B, Chronic - virology
Hepatocellular carcinoma
Humans
Immune tolerance
Immunofluorescence
Immunological tolerance
Infections
Interleukin 10
Investigations
Italy - epidemiology
Kaplan-Meier Estimate
Leukocyte Common Antigens - metabolism
Liver - immunology
Liver - pathology
Liver - surgery
Liver - virology
Liver cancer
Liver Neoplasms - immunology
Liver Neoplasms - mortality
Liver Neoplasms - virology
Lymphocytes
Lymphocytes T
Male
Medical prognosis
Middle Aged
Neonates
Neoplasm Recurrence, Local - epidemiology
Neoplasm Recurrence, Local - immunology
Neoplasm Recurrence, Local - pathology
Paracrine signalling
Primary Cell Culture
Prognosis
Reactive oxygen species
Receptors, Transferrin - metabolism
Retrospective Studies
Risk Assessment - methods
Spleen
Suppressor cells
T cell receptors
T-Lymphocytes - immunology
Tumor Escape
Tumor Microenvironment - immunology
Young Adult
title Intratumoral CD45+CD71+ erythroid cells induce immune tolerance and predict tumor recurrence in hepatocellular carcinoma
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