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DOI . ORG {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Doi.org Make Money
  6. Keywords
  7. Topics
  8. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
  12. Libraries
  13. Hosting Providers
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We began analyzing https://link.springer.com/article/10.1007/s00262-005-0110-x, but it redirected us to https://link.springer.com/article/10.1007/s00262-005-0110-x. The analysis below is for the second page.

Title[redir]:
Tumor escape mechanisms in prostate cancer | Cancer Immunology, Immunotherapy
Description:
Numerous immunotherapy trials have been carried out in prostate cancer (PC) patients, with induction of antigen-specific T cells in some cases. Despite this capability, limited success is seen in terms of tumor regression or survival. In this review, we discuss the evidence for tumor escape strategies that may contribute to vaccine failure in the setting of PC. These include defects in antigen presentation, production of immunosuppressive substances, induction of T cell death, T cell receptor dysfunction, and the presence of tolerogenic dendritic cells and regulatory T cells inside prostate tumors. It is clear that novel strategies aimed at preventing tumor escape, such as small molecular weight inhibitors of immunosuppressive molecules, adoptive transfer of TCR transgenic T cells, removal of Tregs, combined with anti-androgen therapy and prostate-specific vaccines, need to be examined further in PC patients.

Matching Content Categories {๐Ÿ“š}

  • Education
  • Health & Fitness
  • Science

Content Management System {๐Ÿ“}

What CMS is doi.org built with?

Custom-built

No common CMS systems were detected on Doi.org, and no known web development framework was identified.

Traffic Estimate {๐Ÿ“ˆ}

What is the average monthly size of doi.org audience?

๐ŸŒ  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 Doi.org Make Money? {๐Ÿ’ธ}

We see no obvious way the site makes money.

Some websites aren't about earning revenue; they're built to connect communities or raise awareness. There are numerous motivations behind creating websites. This might be one of them. Doi.org might be cashing in, but we can't detect the method they're using.

Keywords {๐Ÿ”}

cancer, google, scholar, pubmed, prostate, cas, article, cells, tumor, res, expression, patients, immunotherapy, cell, dendritic, immunol, urol, human, clin, immune, escape, nitric, oxide, antigen, immunother, interleukin, miller, immunity, carcinoma, synthase, huland, shurin, privacy, cookies, content, pisa, therapy, access, int, vaccination, clinical, factor, gene, urology, lymphocytes, prostatic, liu, growth, regulation, wang,

Topics {โœ’๏ธ}

flt3-ligand/cd40-ligand immunotherapy month download article/chapter article cancer immunology signal-transducing zeta chains transforming growth factor-beta1 hormone-refractory prostate cancer fas/fas ligand interactions tumor-host immune interactions tumor-induced immune dysfunction antigen-loaded dendritic cells influence tumor regression/progression tumour-infiltrating lymphocytes t-lymphocyte subset infiltration monocyte-derived dendritic cells blocking t-cell activation prevents long-term survival prostate-specific vaccines full article pdf high-grade prostate cancer cell-based vaccines psa-based vaccines privacy choices/manage cookies tumour escape van de rijn humoral immune responses recombinant human psa dendritic cell immunotherapy prostate cancer progression primary prostate cancer cell receptor dysfunction nitric oxide synthase nitric oxide synthase-2 human solid tumors orthotopic mouse model /ii clinical trials swedish cancer society human prostate cancer situ gene therapy fas-mediated suicide prostate cancer cells dendritic cell dysfunction transgenic mouse model beta-2 microglobulin expression tolerogenic dendritic cells natural killer cells advanced prostate cancer prostate cancer antigens preventing tumor escape millerย &ย pavel pisa defective antigen processing

Questions {โ“}

  • Antony PA, Restifo NP (2002) Do CD4+ CD25+ immunoregulatory T cells hinder tumor immunotherapy?
  • Lutz MB, Schuler G (2002) Immature, semi-mature and fully mature dendritic cells: which signals induce tolerance or immunity?
  • Pawelec G (2004) Tumour escape: antitumour effectors too much of a good thing?

Schema {๐Ÿ—บ๏ธ}

WebPage:
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         headline:Tumor escape mechanisms in prostate cancer
         description:Numerous immunotherapy trials have been carried out in prostate cancer (PC) patients, with induction of antigen-specific T cells in some cases. Despite this capability, limited success is seen in terms of tumor regression or survival. In this review, we discuss the evidence for tumor escape strategies that may contribute to vaccine failure in the setting of PC. These include defects in antigen presentation, production of immunosuppressive substances, induction of T cell death, T cell receptor dysfunction, and the presence of tolerogenic dendritic cells and regulatory T cells inside prostate tumors. It is clear that novel strategies aimed at preventing tumor escape, such as small molecular weight inhibitors of immunosuppressive molecules, adoptive transfer of TCR transgenic T cells, removal of Tregs, combined with anti-androgen therapy and prostate-specific vaccines, need to be examined further in PC patients.
         datePublished:2005-12-16T00:00:00Z
         dateModified:2005-12-16T00:00:00Z
         pageStart:81
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      headline:Tumor escape mechanisms in prostate cancer
      description:Numerous immunotherapy trials have been carried out in prostate cancer (PC) patients, with induction of antigen-specific T cells in some cases. Despite this capability, limited success is seen in terms of tumor regression or survival. In this review, we discuss the evidence for tumor escape strategies that may contribute to vaccine failure in the setting of PC. These include defects in antigen presentation, production of immunosuppressive substances, induction of T cell death, T cell receptor dysfunction, and the presence of tolerogenic dendritic cells and regulatory T cells inside prostate tumors. It is clear that novel strategies aimed at preventing tumor escape, such as small molecular weight inhibitors of immunosuppressive molecules, adoptive transfer of TCR transgenic T cells, removal of Tregs, combined with anti-androgen therapy and prostate-specific vaccines, need to be examined further in PC patients.
      datePublished:2005-12-16T00:00:00Z
      dateModified:2005-12-16T00:00:00Z
      pageStart:81
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External Links {๐Ÿ”—}(313)

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