Loading…
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...
Saved in:
Published in: | Cancer letters 2021-02, Vol.499, p.85-98 |
---|---|
Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c320t-9e85b64bc05ff75c3de0d5fbc99e7f005a06653066c43b0eb5b80c43170079193 |
---|---|
cites | cdi_FETCH-LOGICAL-c320t-9e85b64bc05ff75c3de0d5fbc99e7f005a06653066c43b0eb5b80c43170079193 |
container_end_page | 98 |
container_issue | |
container_start_page | 85 |
container_title | Cancer letters |
container_volume | 499 |
creator | Chen, Jie Qiao, Yi-Dan Li, Xing Xu, Jian-Liang Ye, Qing-Jian Jiang, Nan Zhang, Hui 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 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2467840901</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0304383520306534</els_id><sourcerecordid>2473386966</sourcerecordid><originalsourceid>FETCH-LOGICAL-c320t-9e85b64bc05ff75c3de0d5fbc99e7f005a06653066c43b0eb5b80c43170079193</originalsourceid><addsrcrecordid>eNp9kU-PFCEQxYnRuOPqNzCGxIvJpseiaZrmYmJm_bPJJl70TGiozjLphhFo4357aWf14MELkOJXj-I9Ql4y2DNg_dvj3powY9m30NZSuwfgj8iODbJtpBrgMdkBh67hAxcX5FnORwAQnRRPyQXnrVR9y3fk500oyZR1icnM9HDdiavDtWRXFNN9uUvRO2pxnjP1wa0WqV-WNSAtccZkQi2Y4OgpofO20N8yNKFdU8Lt0gd6hydT4qaxziZRa5L1IS7mOXkymTnji4f9knz7-OHr4XNz--XTzeH9bWN5C6VROIix70YLYpqksNwhODGNVimUU_2Qgb4XvC624yPgKMYB6pFJAKmY4pfkzVn3lOL3FXPRi8_bOCZgXLNuu14OHShgFX39D3qMawp1ukpJzode9X2lujNlU8w54aRPyS8m3WsGektGH_U5Gb0lo1mrazK17dWD-Dou6P42_YmiAu_OAFY3fnhMOlu_ueh8dbRoF_3_X_gFzfSg6Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2473386966</pqid></control><display><type>article</type><title>Intratumoral CD45+CD71+ erythroid cells induce immune tolerance and predict tumor recurrence in hepatocellular carcinoma</title><source>ScienceDirect Journals</source><creator>Chen, Jie ; Qiao, Yi-Dan ; Li, Xing ; Xu, Jian-Liang ; Ye, Qing-Jian ; Jiang, Nan ; Zhang, Hui ; Wu, Xiang-Yuan</creator><creatorcontrib>Chen, Jie ; Qiao, Yi-Dan ; Li, Xing ; Xu, Jian-Liang ; Ye, Qing-Jian ; Jiang, Nan ; Zhang, Hui ; Wu, Xiang-Yuan</creatorcontrib><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.</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. Published by Elsevier B.V.</rights><rights>Copyright Elsevier Limited Feb 28, 2021</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c320t-9e85b64bc05ff75c3de0d5fbc99e7f005a06653066c43b0eb5b80c43170079193</citedby><cites>FETCH-LOGICAL-c320t-9e85b64bc05ff75c3de0d5fbc99e7f005a06653066c43b0eb5b80c43170079193</cites><orcidid>0000-0001-8237-6113</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33279623$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Jie</creatorcontrib><creatorcontrib>Qiao, Yi-Dan</creatorcontrib><creatorcontrib>Li, Xing</creatorcontrib><creatorcontrib>Xu, Jian-Liang</creatorcontrib><creatorcontrib>Ye, Qing-Jian</creatorcontrib><creatorcontrib>Jiang, Nan</creatorcontrib><creatorcontrib>Zhang, Hui</creatorcontrib><creatorcontrib>Wu, Xiang-Yuan</creatorcontrib><title>Intratumoral CD45+CD71+ erythroid cells induce immune tolerance and predict tumor recurrence in hepatocellular carcinoma</title><title>Cancer letters</title><addtitle>Cancer Lett</addtitle><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.</description><subject>Adult</subject><subject>Aged</subject><subject>Antibodies</subject><subject>Antigens</subject><subject>Antigens, CD - metabolism</subject><subject>Carcinoma, Hepatocellular - immunology</subject><subject>Carcinoma, Hepatocellular - mortality</subject><subject>Carcinoma, Hepatocellular - therapy</subject><subject>Carcinoma, Hepatocellular - virology</subject><subject>CD45 antigen</subject><subject>Cell adhesion</subject><subject>Cell growth</subject><subject>Cells, Cultured</subject><subject>Coculture Techniques</subject><subject>Disease-Free Survival</subject><subject>Erythroid cells</subject><subject>Erythroid Cells - immunology</subject><subject>Erythroid Cells - metabolism</subject><subject>Erythropoiesis</subject><subject>Female</subject><subject>Flow cytometry</subject><subject>Follow-Up Studies</subject><subject>Hematopoiesis, Extramedullary - immunology</subject><subject>Hepatectomy</subject><subject>Hepatitis B</subject><subject>Hepatitis B, Chronic - immunology</subject><subject>Hepatitis B, Chronic - pathology</subject><subject>Hepatitis B, Chronic - virology</subject><subject>Hepatocellular carcinoma</subject><subject>Humans</subject><subject>Immune tolerance</subject><subject>Immunofluorescence</subject><subject>Immunological tolerance</subject><subject>Infections</subject><subject>Interleukin 10</subject><subject>Investigations</subject><subject>Italy - epidemiology</subject><subject>Kaplan-Meier Estimate</subject><subject>Leukocyte Common Antigens - metabolism</subject><subject>Liver - immunology</subject><subject>Liver - pathology</subject><subject>Liver - surgery</subject><subject>Liver - virology</subject><subject>Liver cancer</subject><subject>Liver Neoplasms - immunology</subject><subject>Liver Neoplasms - mortality</subject><subject>Liver Neoplasms - virology</subject><subject>Lymphocytes</subject><subject>Lymphocytes T</subject><subject>Male</subject><subject>Medical prognosis</subject><subject>Middle Aged</subject><subject>Neonates</subject><subject>Neoplasm Recurrence, Local - epidemiology</subject><subject>Neoplasm Recurrence, Local - immunology</subject><subject>Neoplasm Recurrence, Local - pathology</subject><subject>Paracrine signalling</subject><subject>Primary Cell Culture</subject><subject>Prognosis</subject><subject>Reactive oxygen species</subject><subject>Receptors, Transferrin - metabolism</subject><subject>Retrospective Studies</subject><subject>Risk Assessment - methods</subject><subject>Spleen</subject><subject>Suppressor cells</subject><subject>T cell receptors</subject><subject>T-Lymphocytes - immunology</subject><subject>Tumor Escape</subject><subject>Tumor Microenvironment - immunology</subject><subject>Young Adult</subject><issn>0304-3835</issn><issn>1872-7980</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kU-PFCEQxYnRuOPqNzCGxIvJpseiaZrmYmJm_bPJJl70TGiozjLphhFo4357aWf14MELkOJXj-I9Ql4y2DNg_dvj3powY9m30NZSuwfgj8iODbJtpBrgMdkBh67hAxcX5FnORwAQnRRPyQXnrVR9y3fk500oyZR1icnM9HDdiavDtWRXFNN9uUvRO2pxnjP1wa0WqV-WNSAtccZkQi2Y4OgpofO20N8yNKFdU8Lt0gd6hydT4qaxziZRa5L1IS7mOXkymTnji4f9knz7-OHr4XNz--XTzeH9bWN5C6VROIix70YLYpqksNwhODGNVimUU_2Qgb4XvC624yPgKMYB6pFJAKmY4pfkzVn3lOL3FXPRi8_bOCZgXLNuu14OHShgFX39D3qMawp1ukpJzode9X2lujNlU8w54aRPyS8m3WsGektGH_U5Gb0lo1mrazK17dWD-Dou6P42_YmiAu_OAFY3fnhMOlu_ueh8dbRoF_3_X_gFzfSg6Q</recordid><startdate>20210228</startdate><enddate>20210228</enddate><creator>Chen, Jie</creator><creator>Qiao, Yi-Dan</creator><creator>Li, Xing</creator><creator>Xu, Jian-Liang</creator><creator>Ye, Qing-Jian</creator><creator>Jiang, Nan</creator><creator>Zhang, Hui</creator><creator>Wu, Xiang-Yuan</creator><general>Elsevier B.V</general><general>Elsevier Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8237-6113</orcidid></search><sort><creationdate>20210228</creationdate><title>Intratumoral CD45+CD71+ erythroid cells induce immune tolerance and predict tumor recurrence in hepatocellular carcinoma</title><author>Chen, Jie ; Qiao, Yi-Dan ; Li, Xing ; Xu, Jian-Liang ; Ye, Qing-Jian ; Jiang, Nan ; Zhang, Hui ; Wu, Xiang-Yuan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c320t-9e85b64bc05ff75c3de0d5fbc99e7f005a06653066c43b0eb5b80c43170079193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antibodies</topic><topic>Antigens</topic><topic>Antigens, CD - metabolism</topic><topic>Carcinoma, Hepatocellular - immunology</topic><topic>Carcinoma, Hepatocellular - mortality</topic><topic>Carcinoma, Hepatocellular - therapy</topic><topic>Carcinoma, Hepatocellular - virology</topic><topic>CD45 antigen</topic><topic>Cell adhesion</topic><topic>Cell growth</topic><topic>Cells, Cultured</topic><topic>Coculture Techniques</topic><topic>Disease-Free Survival</topic><topic>Erythroid cells</topic><topic>Erythroid Cells - immunology</topic><topic>Erythroid Cells - metabolism</topic><topic>Erythropoiesis</topic><topic>Female</topic><topic>Flow cytometry</topic><topic>Follow-Up Studies</topic><topic>Hematopoiesis, Extramedullary - immunology</topic><topic>Hepatectomy</topic><topic>Hepatitis B</topic><topic>Hepatitis B, Chronic - immunology</topic><topic>Hepatitis B, Chronic - pathology</topic><topic>Hepatitis B, Chronic - virology</topic><topic>Hepatocellular carcinoma</topic><topic>Humans</topic><topic>Immune tolerance</topic><topic>Immunofluorescence</topic><topic>Immunological tolerance</topic><topic>Infections</topic><topic>Interleukin 10</topic><topic>Investigations</topic><topic>Italy - epidemiology</topic><topic>Kaplan-Meier Estimate</topic><topic>Leukocyte Common Antigens - metabolism</topic><topic>Liver - immunology</topic><topic>Liver - pathology</topic><topic>Liver - surgery</topic><topic>Liver - virology</topic><topic>Liver cancer</topic><topic>Liver Neoplasms - immunology</topic><topic>Liver Neoplasms - mortality</topic><topic>Liver Neoplasms - virology</topic><topic>Lymphocytes</topic><topic>Lymphocytes T</topic><topic>Male</topic><topic>Medical prognosis</topic><topic>Middle Aged</topic><topic>Neonates</topic><topic>Neoplasm Recurrence, Local - epidemiology</topic><topic>Neoplasm Recurrence, Local - immunology</topic><topic>Neoplasm Recurrence, Local - pathology</topic><topic>Paracrine signalling</topic><topic>Primary Cell Culture</topic><topic>Prognosis</topic><topic>Reactive oxygen species</topic><topic>Receptors, Transferrin - metabolism</topic><topic>Retrospective Studies</topic><topic>Risk Assessment - methods</topic><topic>Spleen</topic><topic>Suppressor cells</topic><topic>T cell receptors</topic><topic>T-Lymphocytes - immunology</topic><topic>Tumor Escape</topic><topic>Tumor Microenvironment - immunology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Jie</creatorcontrib><creatorcontrib>Qiao, Yi-Dan</creatorcontrib><creatorcontrib>Li, Xing</creatorcontrib><creatorcontrib>Xu, Jian-Liang</creatorcontrib><creatorcontrib>Ye, Qing-Jian</creatorcontrib><creatorcontrib>Jiang, Nan</creatorcontrib><creatorcontrib>Zhang, Hui</creatorcontrib><creatorcontrib>Wu, Xiang-Yuan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Jie</au><au>Qiao, Yi-Dan</au><au>Li, Xing</au><au>Xu, Jian-Liang</au><au>Ye, Qing-Jian</au><au>Jiang, Nan</au><au>Zhang, Hui</au><au>Wu, Xiang-Yuan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intratumoral CD45+CD71+ erythroid cells induce immune tolerance and predict tumor recurrence in hepatocellular carcinoma</atitle><jtitle>Cancer letters</jtitle><addtitle>Cancer Lett</addtitle><date>2021-02-28</date><risdate>2021</risdate><volume>499</volume><spage>85</spage><epage>98</epage><pages>85-98</pages><issn>0304-3835</issn><eissn>1872-7980</eissn><abstract>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.</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> |
fulltext | fulltext |
identifier | ISSN: 0304-3835 |
ispartof | Cancer letters, 2021-02, Vol.499, p.85-98 |
issn | 0304-3835 1872-7980 |
language | eng |
recordid | cdi_proquest_miscellaneous_2467840901 |
source | ScienceDirect Journals |
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 |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T02%3A46%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Intratumoral%20CD45+CD71+%20erythroid%20cells%20induce%20immune%20tolerance%20and%20predict%20tumor%20recurrence%20in%20hepatocellular%20carcinoma&rft.jtitle=Cancer%20letters&rft.au=Chen,%20Jie&rft.date=2021-02-28&rft.volume=499&rft.spage=85&rft.epage=98&rft.pages=85-98&rft.issn=0304-3835&rft.eissn=1872-7980&rft_id=info:doi/10.1016/j.canlet.2020.12.003&rft_dat=%3Cproquest_cross%3E2473386966%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c320t-9e85b64bc05ff75c3de0d5fbc99e7f005a06653066c43b0eb5b80c43170079193%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2473386966&rft_id=info:pmid/33279623&rfr_iscdi=true |