Here's how LINK.SPRINGER.COM makes money* and how much!

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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. Schema
  9. External Links
  10. Analytics And Tracking
  11. Libraries
  12. CDN Services

We are analyzing https://link.springer.com/article/10.1007/s00262-003-0390-y.

Title:
Injection by various routes of melanoma antigen-associated macrophages: biodistribution and clinical effects | Cancer Immunology, Immunotherapy
Description:
Cancer Immunology, Immunotherapy - Patients
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Science
  • Education
  • Health & Fitness

Content Management System {📝}

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 {📈}

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 8,280,528 visitors per month in the current month.

check SE Ranking
check Ahrefs
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check Semrush

How Does Link.springer.com Make Money? {💸}

We're unsure how the site profits.

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 could be secretly minting cash, but we can't detect the process.

Keywords {🔍}

google, scholar, cas, cells, pubmed, cancer, article, dendritic, melanoma, immunol, macrophages, patients, injection, mage, human, lymph, tumor, vitro, res, immunotherapy, lesimple, peptide, moisan, autologous, nodes, access, cell, immunother, lymphocytes, privacy, cookies, content, biodistribution, migration, hlaa, metastatic, cytolytic, rennes, france, publish, search, immunology, clinical, bernard, quillien, toujas, vaccination, antigen, med, expression,

Topics {✒️}

granulocyte-macrophage colony-stimulating factor mage-3-gene-derived peptide-specific cytolytic influenza-matrix peptide-specific cytotoxic comités départementaux d'ille tumour-cytotoxic macrophages generated month download article/chapter human monocyte-derived macrophages leukapheresis-separated mononuclear cells lymphocyte-defined peptide derived claudia lefeuvre-plesse terminal stage hla-a2 hla-a2 induces cytolytic hla-a2+ melanoma patients tumor antigen-specific mage-a1 epitopes recognized antigen-presenting cells melanoma-invaded lymph nodes centre hospitalier régional tumor antigen mage-3 tumor antigens recognized isabelle ollivier related subjects human dendritic cells peripheral blood monocytes activated autologous macrophages article cancer immunology human gene mage-3 full article pdf cultured dendritic cells privacy choices/manage cookies hla-a2 patients antigen-specific cytolytic antitumor immunity human leukocyte antigen dendritic cells transduced murine dendritic cells dendritic cells differentiated determine peptide reactivity understanding dendritic cell circulating blood monocytes recombinant human interleukin cancer staging system peripheral lymph vessel peptide-loaded apc metastatic cutaneous melanoma metastatic renal carcinoma t-lymphocyte traffic adoptive cell transfer antitumour cell therapy european economic area

Schema {🗺️}

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         headline:Injection by various routes of melanoma antigen-associated macrophages: biodistribution and clinical effects
         description:Patients' autologous macrophages (AM) were used as antigen-presenting cells (APC) in a vaccination protocol against malignant melanoma. AM were administered by various routes, including intralymphatic, since these cells did not express CCR7, a molecule required for APC migration to lymph nodes. Seven HLA-A2 patients with metastatic melanoma—two classified as M1 and five as M3—were included in the study. AM were produced from leukapheresis-separated mononuclear cells by 7-day culture with granulocyte-macrophage colony-stimulating factor. After separation by elutriation, AM were frozen in aliquots and subsequently thawed at monthly intervals, exposed to MAGE-3(271–279) peptide and injected subcutaneously into lymph nodes or into one peripheral lymph vessel. Intradermal tests were performed before and after treatment to determine peptide reactivity. No acute toxicity was observed following injection. One M1 patient had a 7-mm induration intradermal reaction response and was stabilized for 64 weeks. The M3 patients did not show any immunological or clinical response. In 11 patients, the biodistribution of 111In-labeled AM was investigated. There was no clear evidence that AM injected intradermally or subcutaneously left the site of injection. After injection into a lymph vessel of the foot region, scintigraphs showed five to ten popliteal and inguinocrural lymph nodes. This appeared to be the most efficient way to administer rapidly and safely large amounts of peptide-loaded APC into lymph nodes.
         datePublished:2003-04-11T00:00:00Z
         dateModified:2003-04-11T00:00:00Z
         pageStart:438
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            Immunotherapy
            Macrophages
            Tumor antigen
            Vaccination
            Radiolabeling
            Oncology
            Immunology
            Cancer Research
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      headline:Injection by various routes of melanoma antigen-associated macrophages: biodistribution and clinical effects
      description:Patients' autologous macrophages (AM) were used as antigen-presenting cells (APC) in a vaccination protocol against malignant melanoma. AM were administered by various routes, including intralymphatic, since these cells did not express CCR7, a molecule required for APC migration to lymph nodes. Seven HLA-A2 patients with metastatic melanoma—two classified as M1 and five as M3—were included in the study. AM were produced from leukapheresis-separated mononuclear cells by 7-day culture with granulocyte-macrophage colony-stimulating factor. After separation by elutriation, AM were frozen in aliquots and subsequently thawed at monthly intervals, exposed to MAGE-3(271–279) peptide and injected subcutaneously into lymph nodes or into one peripheral lymph vessel. Intradermal tests were performed before and after treatment to determine peptide reactivity. No acute toxicity was observed following injection. One M1 patient had a 7-mm induration intradermal reaction response and was stabilized for 64 weeks. The M3 patients did not show any immunological or clinical response. In 11 patients, the biodistribution of 111In-labeled AM was investigated. There was no clear evidence that AM injected intradermally or subcutaneously left the site of injection. After injection into a lymph vessel of the foot region, scintigraphs showed five to ten popliteal and inguinocrural lymph nodes. This appeared to be the most efficient way to administer rapidly and safely large amounts of peptide-loaded APC into lymph nodes.
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      dateModified:2003-04-11T00:00:00Z
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         Melanoma
         Immunotherapy
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         Tumor antigen
         Vaccination
         Radiolabeling
         Oncology
         Immunology
         Cancer Research
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      name:Centre Régional de Lutte Contre le Cancer Eugène Marquis, Rennes, France
      name:Centre Régional de Lutte Contre le Cancer Eugène Marquis, Rennes, France
      name:Centre Régional de Lutte Contre le Cancer Eugène Marquis, Rennes, France
      name:Service de Dermatologie, Centre Hospitalier Régional, Rennes, France
      name:Service d'Oncologie médicale, Centre Hospitalier Régional, Grenoble, France
      name:Centre Régional de Lutte Contre le Cancer Eugène Marquis, Rennes, France
      name:Etablissement de Transfusion Sanguine, Rennes, France
      name:Centre Régional de Lutte Contre le Cancer Eugène Marquis, Rennes, France
      name:Centre Régional de Lutte Contre le Cancer Eugène Marquis, Rennes, France
      name:Laboratoire d'immuno-hématologie, Centre Hospitalier Régional, Rennes, France
      name:Centre Régional de Lutte Contre le Cancer Eugène Marquis, Rennes, France
      name:Service de Dermatologie, Centre Hospitalier Régional, Rennes, France
      name:Centre Régional de Lutte Contre le Cancer Eugène Marquis, Rennes, France
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