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LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
  12. Libraries
  13. CDN Services

We are analyzing https://link.springer.com/article/10.1007/s11427-017-9176-7.

Title:
The role of T-cell immunoglobulin mucin-3 and its ligand galectin-9 in antitumor immunity and cancer immunotherapy | Science China Life Sciences
Description:
Cancer treatment in the past few years has been transformed by a new kind of therapy that targets the immune system instead of the cancer itself to reinvigorate antitumor immunity with astonishing results. However, primary and acquired resistance to this type of treatment, namely immune checkpoint blockade (ICB), continue to counter treatment efficacy. In many cases, resistance has been attributed to defective or chronically enhanced interferon signaling and/or upregulation of alternative immune checkpoints, including T-cell immunoglobulin mucin-3 (Tim-3) and its ligand galactin-9 (Gal-9). In this article, we briefly describe the current knowledge of common checkpoint resistance mechanisms, focusing on the Tim-3/Gal-9 pathway as an alternative checkpoint that holds great promise as another target for ICB.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Education
  • Health & Fitness
  • Science

Content Management System {πŸ“}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {πŸ“ˆ}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
However, some sources were not loaded, we suggest to reload the page to get complete results.

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How Does Link.springer.com Make Money? {πŸ’Έ}

We see no obvious way the site makes money.

The purpose of some websites isn't monetary gain; they're meant to inform, educate, or foster collaboration. Everyone has unique reasons for building websites. This could be an example. Link.springer.com could be secretly minting cash, but we can't detect the process.

Keywords {πŸ”}

pubmed, article, google, scholar, cas, cancer, central, cell, immunol, tim, galectin, immune, cells, nat, immunity, immunotherapy, kuchroo, tcell, resistance, rev, lee, hirashima, tumor, type, blockade, regulates, mucin, yang, hung, checkpoint, interferon, signaling, china, access, freeman, sci, anderson, research, ligand, protein, human, usa, wang, med, zhu, schreiber, chen, university, privacy, cookies,

Topics {βœ’οΈ}

ifnΞ³-dependent tissue-immune homeostasis mrl/lpr lupus-prone mice galectin-9-independent ligand-binding surface month download article/chapter suppress t-cell proliferation international research-intensive centers nuclear factor-kappab activation t-cell immunoglobulin mucin-3 mesenchymal stem/stromal cells mien-chie hung cd8 t-cell responses innate immune sensing calcium-calpain-caspase-1 pathway beta-galactoside binding lectin cd8 t-cell exhaustion china life sci regulating anti-tumor immunity china medical university tumor-infiltrating tim-3 virus-specific humoral ifn-Ξ³ pathway genes peritumoral immune tolerance full article pdf cd44 reciprocally regulates growing tumors induce t-cell exhaustion tim-3 mediates phagocytosis tim-3 ligand regulates privacy choices/manage cookies therapeutic pd-1 blockade alternative immune checkpoints article yang immune checkpoint blockade immune-checkpoint blockade related subjects chronic viral infection shape tumour immunogenicity encephalitogenic th1/th17 th1-suppressive effects phosphoinositide 3-kinase pathway experimental autoimmune encephalomyelitis interferon receptor promotes galectin-9 induces apoptosis emerging therapeutic targets phosphotyrosine-dependent coupling immune checkpoint target tim-3/gal-9 pathway impaired interferon signaling common immune defect tumor-intrinsic

Questions {❓}

  • Antigen-independent induction of Tim-3 expression on human T cells by the common?
  • Galectins and immune responses-just how do they do those things they do?

Schema {πŸ—ΊοΈ}

WebPage:
      mainEntity:
         headline:The role of T-cell immunoglobulin mucin-3 and its ligand galectin-9 in antitumor immunity and cancer immunotherapy
         description:Cancer treatment in the past few years has been transformed by a new kind of therapy that targets the immune system instead of the cancer itself to reinvigorate antitumor immunity with astonishing results. However, primary and acquired resistance to this type of treatment, namely immune checkpoint blockade (ICB), continue to counter treatment efficacy. In many cases, resistance has been attributed to defective or chronically enhanced interferon signaling and/or upregulation of alternative immune checkpoints, including T-cell immunoglobulin mucin-3 (Tim-3) and its ligand galactin-9 (Gal-9). In this article, we briefly describe the current knowledge of common checkpoint resistance mechanisms, focusing on the Tim-3/Gal-9 pathway as an alternative checkpoint that holds great promise as another target for ICB.
         datePublished:2017-10-11T00:00:00Z
         dateModified:2017-10-11T00:00:00Z
         pageStart:1058
         pageEnd:1064
         sameAs:https://doi.org/10.1007/s11427-017-9176-7
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         author:
               name:Riyao Yang
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                     name:The University of Texas MD Anderson Cancer Center
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                        name:Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
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               name:Mien-Chie Hung
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                     name:The University of Texas MD Anderson Cancer Center
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ScholarlyArticle:
      headline:The role of T-cell immunoglobulin mucin-3 and its ligand galectin-9 in antitumor immunity and cancer immunotherapy
      description:Cancer treatment in the past few years has been transformed by a new kind of therapy that targets the immune system instead of the cancer itself to reinvigorate antitumor immunity with astonishing results. However, primary and acquired resistance to this type of treatment, namely immune checkpoint blockade (ICB), continue to counter treatment efficacy. In many cases, resistance has been attributed to defective or chronically enhanced interferon signaling and/or upregulation of alternative immune checkpoints, including T-cell immunoglobulin mucin-3 (Tim-3) and its ligand galactin-9 (Gal-9). In this article, we briefly describe the current knowledge of common checkpoint resistance mechanisms, focusing on the Tim-3/Gal-9 pathway as an alternative checkpoint that holds great promise as another target for ICB.
      datePublished:2017-10-11T00:00:00Z
      dateModified:2017-10-11T00:00:00Z
      pageStart:1058
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      sameAs:https://doi.org/10.1007/s11427-017-9176-7
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         cancer
         Tim-3
         galectin-9
         immune checkpoints
         immunotherapy
         Life Sciences
         general
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         name:Science China Life Sciences
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      author:
            name:Riyao Yang
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                  name:The University of Texas MD Anderson Cancer Center
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                     name:Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Mien-Chie Hung
            affiliation:
                  name:The University of Texas MD Anderson Cancer Center
                  address:
                     name:Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
                     type:PostalAddress
                  type:Organization
                  name:China Medical University
                  address:
                     name:Center for Molecular Medicine and Graduate Institute of Biomedical Sciences, China Medical University, Taichung, China
                     type:PostalAddress
                  type:Organization
                  name:Asia University
                  address:
                     name:Department of Biotechnology, Asia University, Taichung, China
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      name:The University of Texas MD Anderson Cancer Center
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         name:Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
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      address:
         name:Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
         type:PostalAddress
      name:China Medical University
      address:
         name:Center for Molecular Medicine and Graduate Institute of Biomedical Sciences, China Medical University, Taichung, China
         type:PostalAddress
      name:Asia University
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         name:Department of Biotechnology, Asia University, Taichung, China
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            address:
               name:Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
               type:PostalAddress
            type:Organization
      name:Mien-Chie Hung
      affiliation:
            name:The University of Texas MD Anderson Cancer Center
            address:
               name:Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
               type:PostalAddress
            type:Organization
            name:China Medical University
            address:
               name:Center for Molecular Medicine and Graduate Institute of Biomedical Sciences, China Medical University, Taichung, China
               type:PostalAddress
            type:Organization
            name:Asia University
            address:
               name:Department of Biotechnology, Asia University, Taichung, China
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Center for Molecular Medicine and Graduate Institute of Biomedical Sciences, China Medical University, Taichung, China
      name:Department of Biotechnology, Asia University, Taichung, China
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External Links {πŸ”—}(288)

Analytics and Tracking {πŸ“Š}

  • Google Tag Manager

Libraries {πŸ“š}

  • Clipboard.js
  • Prism.js

CDN Services {πŸ“¦}

  • Crossref

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