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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/10.1385/ir:36:1:247.

Title:
Human tumor-derived vs dendritic cell-derived exosomes have distinct biologic roles and molecular profiles | Immunologic Research
Description:
Microvesicles (MV) or exosomes are produced and secreted by tumor and normal cells. The molecular profile and functions of tumor-derived vs dendritic cell (DC)-derived MV are distinct. The former express death ligands and mediate apoptosis of activated T cells. The latter promote CD4+T cell proliferation and may play a role in regulating T cell responses. Serving as intercellular communication networks, tumor-derived MV contribute to tumor escape, while DC-derived MV drive and regulate immune response.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Science
  • Education
  • Telecommunications

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}

The income method remains a mystery to us.

Many websites are intended to earn money, but some serve to share ideas or build connections. Websites exist for all kinds of purposes. This might be one of them. Link.springer.com might be making money, but it's not detectable how they're doing it.

Keywords {πŸ”}

article, google, scholar, cas, exosomes, pubmed, cells, dendritic, cancer, whiteside, cell, human, access, tumorderived, cellderived, microvesicles, tumor, privacy, cookies, content, research, apoptosis, immune, taylor, immunol, res, publish, search, wieckowski, theresa, open, biol, pittsburgh, function, data, information, log, journal, distinct, roles, molecular, role, escape, discover, plasma, membrane, vesicles, signaling, nat, zitvogel,

Topics {βœ’οΈ}

myeloid-derived suppressor cells dendritic cell-derived exosomes month download article/chapter t-cell signaling defects dendritic cell-derived dendritic cells cells apoptosis access fasl+membraneous vesicles isolated human tumor-derived tumor-derived mv contribute express death ligands dendritic cell related subjects dc-derived mv drive tumor-infiltrating lymphocytes taylor dd cell-free vaccine full article pdf established murine tumors privacy choices/manage cookies tumor cell secretion fasl-bearing microvesicles tumor-derived exosomes immune cells normal cells pittsburgh cancer institute tumour-derived exosomes article wieckowski european economic area intercellular communication networks plasma membrane vesicles plasma membrane fragments plasma membrane activities future therapeutic interventions conditions privacy policy regulate immune response host immune system accepting optional cookies cells check access instant access article log molecular profiles published gercel-taylor distinct biologic roles tumor-derived main content log tumor vaccine whiteside tl article cite

Questions {❓}

  • Tumour-derived exosomes or microvesicles: another mechanism of tumour escape from the host immune system?

Schema {πŸ—ΊοΈ}

WebPage:
      mainEntity:
         headline:Human tumor-derived vs dendritic cell-derived exosomes have distinct biologic roles and molecular profiles
         description:Microvesicles (MV) or exosomes are produced and secreted by tumor and normal cells. The molecular profile and functions of tumor-derived vs dendritic cell (DC)-derived MV are distinct. The former express death ligands and mediate apoptosis of activated T cells. The latter promote CD4+T cell proliferation and may play a role in regulating T cell responses. Serving as intercellular communication networks, tumor-derived MV contribute to tumor escape, while DC-derived MV drive and regulate immune response.
         datePublished:
         dateModified:
         pageStart:247
         pageEnd:254
         sameAs:https://doi.org/10.1385/IR:36:1:247
         keywords:
            Exosomes
            Microvesicles
            Human tumors
            Dendritic cells
            T cells
            Apoptosis
            Immunology
            Allergology
            Medicine/Public Health
            general
            Internal Medicine
         image:
         isPartOf:
            name:Immunologic Research
            issn:
               1559-0755
               0257-277X
            volumeNumber:36
            type:
               Periodical
               PublicationVolume
         publisher:
            name:Humana Press
            logo:
               url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
               type:ImageObject
            type:Organization
         author:
               name:Eva Wieckowski
               affiliation:
                     name:University of Pittsburgh School of Medicine
                     address:
                        name:Department of Pathology, Immunology and Otolaryngology, University of Pittsburgh School of Medicine, Pittsburgh, USA
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Theresa L. Whiteside
               affiliation:
                     name:University of Pittsburgh School of Medicine
                     address:
                        name:Department of Pathology, Immunology and Otolaryngology, University of Pittsburgh School of Medicine, Pittsburgh, USA
                        type:PostalAddress
                     type:Organization
                     name:University of Pittsburgh Cancer Institute
                     address:
                        name:Hillman Cancer Center, University of Pittsburgh Cancer Institute, Pittsburgh
                        type:PostalAddress
                     type:Organization
               email:whitesidelt@upmc edu
               type:Person
         isAccessibleForFree:
         hasPart:
            isAccessibleForFree:
            cssSelector:.main-content
            type:WebPageElement
         type:ScholarlyArticle
      context:https://schema.org
ScholarlyArticle:
      headline:Human tumor-derived vs dendritic cell-derived exosomes have distinct biologic roles and molecular profiles
      description:Microvesicles (MV) or exosomes are produced and secreted by tumor and normal cells. The molecular profile and functions of tumor-derived vs dendritic cell (DC)-derived MV are distinct. The former express death ligands and mediate apoptosis of activated T cells. The latter promote CD4+T cell proliferation and may play a role in regulating T cell responses. Serving as intercellular communication networks, tumor-derived MV contribute to tumor escape, while DC-derived MV drive and regulate immune response.
      datePublished:
      dateModified:
      pageStart:247
      pageEnd:254
      sameAs:https://doi.org/10.1385/IR:36:1:247
      keywords:
         Exosomes
         Microvesicles
         Human tumors
         Dendritic cells
         T cells
         Apoptosis
         Immunology
         Allergology
         Medicine/Public Health
         general
         Internal Medicine
      image:
      isPartOf:
         name:Immunologic Research
         issn:
            1559-0755
            0257-277X
         volumeNumber:36
         type:
            Periodical
            PublicationVolume
      publisher:
         name:Humana Press
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:Eva Wieckowski
            affiliation:
                  name:University of Pittsburgh School of Medicine
                  address:
                     name:Department of Pathology, Immunology and Otolaryngology, University of Pittsburgh School of Medicine, Pittsburgh, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Theresa L. Whiteside
            affiliation:
                  name:University of Pittsburgh School of Medicine
                  address:
                     name:Department of Pathology, Immunology and Otolaryngology, University of Pittsburgh School of Medicine, Pittsburgh, USA
                     type:PostalAddress
                  type:Organization
                  name:University of Pittsburgh Cancer Institute
                  address:
                     name:Hillman Cancer Center, University of Pittsburgh Cancer Institute, Pittsburgh
                     type:PostalAddress
                  type:Organization
            email:whitesidelt@upmc edu
            type:Person
      isAccessibleForFree:
      hasPart:
         isAccessibleForFree:
         cssSelector:.main-content
         type:WebPageElement
["Periodical","PublicationVolume"]:
      name:Immunologic Research
      issn:
         1559-0755
         0257-277X
      volumeNumber:36
Organization:
      name:Humana Press
      logo:
         url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
         type:ImageObject
      name:University of Pittsburgh School of Medicine
      address:
         name:Department of Pathology, Immunology and Otolaryngology, University of Pittsburgh School of Medicine, Pittsburgh, USA
         type:PostalAddress
      name:University of Pittsburgh School of Medicine
      address:
         name:Department of Pathology, Immunology and Otolaryngology, University of Pittsburgh School of Medicine, Pittsburgh, USA
         type:PostalAddress
      name:University of Pittsburgh Cancer Institute
      address:
         name:Hillman Cancer Center, University of Pittsburgh Cancer Institute, Pittsburgh
         type:PostalAddress
ImageObject:
      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:Eva Wieckowski
      affiliation:
            name:University of Pittsburgh School of Medicine
            address:
               name:Department of Pathology, Immunology and Otolaryngology, University of Pittsburgh School of Medicine, Pittsburgh, USA
               type:PostalAddress
            type:Organization
      name:Theresa L. Whiteside
      affiliation:
            name:University of Pittsburgh School of Medicine
            address:
               name:Department of Pathology, Immunology and Otolaryngology, University of Pittsburgh School of Medicine, Pittsburgh, USA
               type:PostalAddress
            type:Organization
            name:University of Pittsburgh Cancer Institute
            address:
               name:Hillman Cancer Center, University of Pittsburgh Cancer Institute, Pittsburgh
               type:PostalAddress
            type:Organization
      email:whitesidelt@upmc edu
PostalAddress:
      name:Department of Pathology, Immunology and Otolaryngology, University of Pittsburgh School of Medicine, Pittsburgh, USA
      name:Department of Pathology, Immunology and Otolaryngology, University of Pittsburgh School of Medicine, Pittsburgh, USA
      name:Hillman Cancer Center, University of Pittsburgh Cancer Institute, Pittsburgh
WebPageElement:
      isAccessibleForFree:
      cssSelector:.main-content

External Links {πŸ”—}(77)

Analytics and Tracking {πŸ“Š}

  • Google Tag Manager

Libraries {πŸ“š}

  • Clipboard.js
  • Prism.js

CDN Services {πŸ“¦}

  • Crossref

4.29s.