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作 者:Xuechun Wang Anna Juncker-Jensen Gang Huang Mate Levente Nagy Xuemin Lu Liang Cheng Xin Lu
机构地区:[1]Department of Biological Sciences,Boler-Parseghian Center for Rare and Neglected Diseases,Harper Cancer Research Institute,University of Notre Dame,Notre Dame,IN,USA [2]NeoGenomics Laboratories,Inc.,Aliso Viejo,CA,USA [3]Department of Pathology and Laboratory Medicine,Brown University Warren Alpert Medical School,Lifespan Academic Medical Center,Legorreta Cancer Center at Brown University,Providence,RI,USA [4]Tumor Microenvironment and Metastasis Program,Indiana University Melvin and Bren Simon Comprehensive Cancer Center,Indianapolis,IN,USA
出 处:《Cancer Communications》2024年第4期499-503,共5页癌症通讯(英文)
基 金:supported by National Institutes of Health grants(R01CA248033 and R01CA280097);Department of Defense Congressionally Directed Medical Research Programs grants(W81XWH2010312,W81XWH2010332 and HT94252310010).
摘 要:Dear Editor,Tertiary lymphoid structures(TLSs)are organized clus-ters of immune cells found in non-lymphoid tissues of chronic inflammation,including solid tumors[1].High endothelial venules(HEVs)positive for peripheral node addressin(PNAd)are present in TLSs and may pro-vide highway entry for lymphocytes.Tumor-residing TLSs may be formed by the concerted actions of cytokines and chemokines,a finding supported by the relation between a 12-chemokine signature and TLSs[2].
关 键 词:BLADDER LYMPHOID inflammation
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