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We are analyzing https://link.springer.com/article/10.1007/s00262-008-0463-z.

Title:
Development of a Listeria monocytogenes based vaccine against prostate cancer | Cancer Immunology, Immunotherapy
Description:
Prostate specific antigen (PSA) is a likely immunotherapeutic target antigen for prostate cancer, the second leading cause of cancer-related death in American men. Previously, we demonstrated that attenuated strains of Listeria monocytogenes (Lm) can be used as effective vaccine vectors for delivery of tumor antigens causing regression of established tumors accompanied by strong immune responses toward these antigens in murine models of cancer. In the present study, we have developed and characterized a recombinant live attenuated L. monocytogenes/PSA (Lm–LLO–PSA) vaccine with potential use for the treatment of pCa. Human PSA gene was cloned into and expressed by an attenuated Lm strain. This recombinant bacterial vaccine, Lm–LLO–PSA was tested for stability, virulence, immunogenicity and anti-tumor effects in a murine model for pCa. Immunization with Lm–LLO–PSA was shown to lower the number of tumor infiltrating T regulatory cells and cause complete regression of over 80% of tumors formed by an implanted genetically modified mouse prostate adenocarcinoma cell line, which expressed human PSA. Lm–LLO–PSA was immunogenic in C57BL/6 mice and splenocytes from mice immunized with Lm–LLO–PSA showed significantly higher number of IFN-γ secreting cells over that of the naĆÆve animals in response to a PSA H2Db-specific peptide, as measured by both, ELISpot and intracellular cytokine staining. In addition, using a CTL assay we show that the T cells specific for PSA were able to recognize and lyse PSA-peptide pulsed target cells in vitro. In a comparison study with two other PSA-based vaccines (a pDNA and a vaccinia vaccine), Lm–LLO–PSA was shown to be more efficacious in regressing established tumors when used in a homologues prime/boost regimen. Together, these results indicate that Lm–LLO–PSA is a potential candidate for pCa immunotherapy and should be further developed.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {šŸ“š}

  • Science
  • Health & Fitness
  • Education

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What CMS is link.springer.com built with?

Custom-built

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Traffic Estimate {šŸ“ˆ}

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🌠 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.
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How Does Link.springer.com Make Money? {šŸ’ø}

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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 cashing in, but we can't detect the method they're using.

Keywords {šŸ”}

google, scholar, article, pubmed, cancer, cas, prostate, vaccine, cells, listeria, immunol, monocytogenes, psa, antigen, immune, human, responses, recombinant, patients, listeriolysin, tumor, tumors, lmllopsa, cell, vaccines, immunotherapy, dendritic, clin, res, prostatespecific, privacy, cookies, content, paterson, regression, established, mouse, access, phase, dna, usa, immunother, publish, research, search, shahabi, attenuated, study, immunogenicity, antitumor,

Topics {āœ’ļø}

month download article/chapter hormone-refractory prostate cancer listeria monocytogenes-based vaccines recombinant live attenuated human prostate-specific antigen psa h2db-specific peptide homologues prime/boost regimen europium-labelled target cells listeria-based vaccines psa-based vaccines ifn-γ secreting cells immunotherapeutic target antigen pox psa vaccines recombinant bacterial vaccine prostate-specific antigen article cancer immunology live animal hosts recombinant human psa vaccinia viruses expressing full article pdf metastatic prostate cancer human papilloma virus-16 attenuated lm strain prostate specific antigens cancer-related death vaccine versus vaccine privacy choices/manage cookies psa-specific ctls effective vaccine vectors antigen density presented metastatic prostate tumors t-cell responses related subjects anti-tumor effects lm–llo–psa restricted ctl epitope anti-tumor immunity listeria monocytogenes enhances bioengineered listeria monocytogenes listeria monocytogenes pathogenicity cd4+cd25+ regulatory human psa gene circumventing immunoregulatory cells th1-type immunity strong immune responses humoral immune responses european economic area future diagnostic markers reveals subdominant epitopes immunodominant h-2d

Questions {ā“}

  • Katz MH, McKiernan JM (2007) High-risk, clinically localized prostate cancer: is monotherapy adequate?
  • Yu P, Fu YX (2006) Tumor-infiltrating T lymphocytes: friends or foes?

Schema {šŸ—ŗļø}

WebPage:
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         headline:Development of a Listeria monocytogenes based vaccine against prostate cancer
         description:Prostate specific antigen (PSA) is a likely immunotherapeutic target antigen for prostate cancer, the second leading cause of cancer-related death in American men. Previously, we demonstrated that attenuated strains of Listeria monocytogenes (Lm) can be used as effective vaccine vectors for delivery of tumor antigens causing regression of established tumors accompanied by strong immune responses toward these antigens in murine models of cancer. In the present study, we have developed and characterized a recombinant live attenuated L. monocytogenes/PSA (Lm–LLO–PSA) vaccine with potential use for the treatment of pCa. Human PSA gene was cloned into and expressed by an attenuated Lm strain. This recombinant bacterial vaccine, Lm–LLO–PSA was tested for stability, virulence, immunogenicity and anti-tumor effects in a murine model for pCa. Immunization with Lm–LLO–PSA was shown to lower the number of tumor infiltrating T regulatory cells and cause complete regression of over 80% of tumors formed by an implanted genetically modified mouse prostate adenocarcinoma cell line, which expressed human PSA. Lm–LLO–PSA was immunogenic in C57BL/6 mice and splenocytes from mice immunized with Lm–LLO–PSA showed significantly higher number of IFN-γ secreting cells over that of the naĆÆve animals in response to a PSA H2Db-specific peptide, as measured by both, ELISpot and intracellular cytokine staining. In addition, using a CTL assay we show that the T cells specific for PSA were able to recognize and lyse PSA-peptide pulsed target cells in vitro. In a comparison study with two other PSA-based vaccines (a pDNA and a vaccinia vaccine), Lm–LLO–PSA was shown to be more efficacious in regressing established tumors when used in a homologues prime/boost regimen. Together, these results indicate that Lm–LLO–PSA is a potential candidate for pCa immunotherapy and should be further developed.
         datePublished:2008-02-14T00:00:00Z
         dateModified:2008-02-14T00:00:00Z
         pageStart:1301
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            Cancer vaccine
            Immunotherapeutic
            Listeriolysin O
            Oncology
            Immunology
            Cancer Research
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      headline:Development of a Listeria monocytogenes based vaccine against prostate cancer
      description:Prostate specific antigen (PSA) is a likely immunotherapeutic target antigen for prostate cancer, the second leading cause of cancer-related death in American men. Previously, we demonstrated that attenuated strains of Listeria monocytogenes (Lm) can be used as effective vaccine vectors for delivery of tumor antigens causing regression of established tumors accompanied by strong immune responses toward these antigens in murine models of cancer. In the present study, we have developed and characterized a recombinant live attenuated L. monocytogenes/PSA (Lm–LLO–PSA) vaccine with potential use for the treatment of pCa. Human PSA gene was cloned into and expressed by an attenuated Lm strain. This recombinant bacterial vaccine, Lm–LLO–PSA was tested for stability, virulence, immunogenicity and anti-tumor effects in a murine model for pCa. Immunization with Lm–LLO–PSA was shown to lower the number of tumor infiltrating T regulatory cells and cause complete regression of over 80% of tumors formed by an implanted genetically modified mouse prostate adenocarcinoma cell line, which expressed human PSA. Lm–LLO–PSA was immunogenic in C57BL/6 mice and splenocytes from mice immunized with Lm–LLO–PSA showed significantly higher number of IFN-γ secreting cells over that of the naĆÆve animals in response to a PSA H2Db-specific peptide, as measured by both, ELISpot and intracellular cytokine staining. In addition, using a CTL assay we show that the T cells specific for PSA were able to recognize and lyse PSA-peptide pulsed target cells in vitro. In a comparison study with two other PSA-based vaccines (a pDNA and a vaccinia vaccine), Lm–LLO–PSA was shown to be more efficacious in regressing established tumors when used in a homologues prime/boost regimen. Together, these results indicate that Lm–LLO–PSA is a potential candidate for pCa immunotherapy and should be further developed.
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          Listeria monocytogenes
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         Cancer vaccine
         Immunotherapeutic
         Listeriolysin O
         Oncology
         Immunology
         Cancer Research
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