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  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
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We are analyzing https://link.springer.com/article/10.1007/s00262-008-0596-0.

Title:
Low-dose radiation enhances therapeutic HPV DNA vaccination in tumor-bearing hosts | Cancer Immunology, Immunotherapy
Description:
Current therapeutic approaches to treatment of patients with bulky cervical cancer are based on conventional in situ ablative modalities including cisplatin-based chemotherapy and radiation therapy. The 5-year survival of patients with nonresectable disease is dismal. Because over 99% of squamous cervical cancer is caused by persistent infection with an oncogenic strain of human papillomavirus (HPV), particularly type 16 and viral oncoproteins E6 and E7 are functionally required for disease initiation and persistence, HPV-targeted immune strategies present a compelling opportunity in which to demonstrate proof of principle. Sublethal doses of radiation and chemotherapeutic agents have been shown to have synergistic effect in combination with either vaccination against cancer-specific antigens, or with passive transfer of tumor-specific cytotoxic T lymphocytes (CTLs). Here, we explored the combination of low-dose radiation therapy with DNA vaccination with calreticulin (CRT) linked to the mutated form of HPV-16 E7 antigen (E7(detox)), CRT/E7(detox) in the treatment of E7-expressing TC-1 tumors. We observed that TC-1 tumor-bearing mice treated with radiotherapy combined with CRT/E7(detox) DNA vaccination generated significant therapeutic antitumor effects and the highest frequency of E7-specific CD8+ T cells in the tumors and spleens of treated mice. Furthermore, treatment with radiotherapy was shown to render the TC-1 tumor cells more susceptible to lysis by E7-specific CTLs. In addition, we observed that treatment with radiotherapy during the second DNA vaccination generated the highest frequency of E7-specific CD8+ T cells in the tumors and spleens of TC-1 tumor-bearing mice. Finally, TC-1 tumor-bearing mice treated with the chemotherapy in combination with radiation and CRT/E7(detox) DNA vaccination generate significantly enhanced therapeutic antitumor effects. The clinical implications of the study are discussed.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Science
  • Health & Fitness
  • Education

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

The income method remains a mystery to us.

Websites don't always need to be profitable; some serve as platforms for education or personal expression. Websites can serve multiple purposes. And this might be one of them. Link.springer.com has a secret sauce for making money, but we can't detect it yet.

Keywords {πŸ”}

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Topics {βœ’οΈ}

radiation-induced ifn-{gamma} production low-dose radiation therapy month download article/chapter ctl-mediated killing endosomal/lysosomal compartment enhances e7-expressing tc-1 tumors dna vaccine potency therapeutic hpv vaccines tc-1 tumor-bearing mice dna vaccination generated e7-specific cd8+ heat shock-sensitive expression dna vaccines combining enhances mhc class tumor-bearing hosts article cancer immunology tumor-specific immunity p53 cancer vaccine recombinant cancer vaccine hpv-16 e7 antigen cisplatin-treated tumors hla-a24Β +Β hrpc patients full article pdf low dose dna vaccines viral recombinant vaccines peptide-specific immunity privacy choices/manage cookies therapeutic vaccines e7-specific ctls human papillomavirus dna vaccination cancer-specific antigens squamous cervical cancer human endothelial cells antitumor immunity article tseng tumor-specific cytotoxic mei-cheng wang individualized peptide vaccination bulky cervical cancer animal tumor model tumor stroma leads metastatic breast cancer immunotherapy aims kaohsiung medical center tc-1 tumor cells enhanced killing viral oncoproteins e6 liu sj

Schema {πŸ—ΊοΈ}

WebPage:
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         headline:Low-dose radiation enhances therapeutic HPV DNA vaccination in tumor-bearing hosts
         description:Current therapeutic approaches to treatment of patients with bulky cervical cancer are based on conventional in situ ablative modalities including cisplatin-based chemotherapy and radiation therapy. The 5-year survival of patients with nonresectable disease is dismal. Because over 99% of squamous cervical cancer is caused by persistent infection with an oncogenic strain of human papillomavirus (HPV), particularly type 16 and viral oncoproteins E6 and E7 are functionally required for disease initiation and persistence, HPV-targeted immune strategies present a compelling opportunity in which to demonstrate proof of principle. Sublethal doses of radiation and chemotherapeutic agents have been shown to have synergistic effect in combination with either vaccination against cancer-specific antigens, or with passive transfer of tumor-specific cytotoxic T lymphocytes (CTLs). Here, we explored the combination of low-dose radiation therapy with DNA vaccination with calreticulin (CRT) linked to the mutated form of HPV-16 E7 antigen (E7(detox)), CRT/E7(detox) in the treatment of E7-expressing TC-1 tumors. We observed that TC-1 tumor-bearing mice treated with radiotherapy combined with CRT/E7(detox) DNA vaccination generated significant therapeutic antitumor effects and the highest frequency of E7-specific CD8+ T cells in the tumors and spleens of treated mice. Furthermore, treatment with radiotherapy was shown to render the TC-1 tumor cells more susceptible to lysis by E7-specific CTLs. In addition, we observed that treatment with radiotherapy during the second DNA vaccination generated the highest frequency of E7-specific CD8+ T cells in the tumors and spleens of TC-1 tumor-bearing mice. Finally, TC-1 tumor-bearing mice treated with the chemotherapy in combination with radiation and CRT/E7(detox) DNA vaccination generate significantly enhanced therapeutic antitumor effects. The clinical implications of the study are discussed.
         datePublished:2008-09-25T00:00:00Z
         dateModified:2008-09-25T00:00:00Z
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            Human papillomavirus
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            Oncology
            Immunology
            Cancer Research
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      headline:Low-dose radiation enhances therapeutic HPV DNA vaccination in tumor-bearing hosts
      description:Current therapeutic approaches to treatment of patients with bulky cervical cancer are based on conventional in situ ablative modalities including cisplatin-based chemotherapy and radiation therapy. The 5-year survival of patients with nonresectable disease is dismal. Because over 99% of squamous cervical cancer is caused by persistent infection with an oncogenic strain of human papillomavirus (HPV), particularly type 16 and viral oncoproteins E6 and E7 are functionally required for disease initiation and persistence, HPV-targeted immune strategies present a compelling opportunity in which to demonstrate proof of principle. Sublethal doses of radiation and chemotherapeutic agents have been shown to have synergistic effect in combination with either vaccination against cancer-specific antigens, or with passive transfer of tumor-specific cytotoxic T lymphocytes (CTLs). Here, we explored the combination of low-dose radiation therapy with DNA vaccination with calreticulin (CRT) linked to the mutated form of HPV-16 E7 antigen (E7(detox)), CRT/E7(detox) in the treatment of E7-expressing TC-1 tumors. We observed that TC-1 tumor-bearing mice treated with radiotherapy combined with CRT/E7(detox) DNA vaccination generated significant therapeutic antitumor effects and the highest frequency of E7-specific CD8+ T cells in the tumors and spleens of treated mice. Furthermore, treatment with radiotherapy was shown to render the TC-1 tumor cells more susceptible to lysis by E7-specific CTLs. In addition, we observed that treatment with radiotherapy during the second DNA vaccination generated the highest frequency of E7-specific CD8+ T cells in the tumors and spleens of TC-1 tumor-bearing mice. Finally, TC-1 tumor-bearing mice treated with the chemotherapy in combination with radiation and CRT/E7(detox) DNA vaccination generate significantly enhanced therapeutic antitumor effects. The clinical implications of the study are discussed.
      datePublished:2008-09-25T00:00:00Z
      dateModified:2008-09-25T00:00:00Z
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         Radiation
         Human papillomavirus
         DNA vaccine
         Calreticulin
         E7
         Oncology
         Immunology
         Cancer Research
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                  name:Chang Gung Memorial Hospital, Kaohsiung Medical Center, Chang Gung University College of Medicine
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                     type:PostalAddress
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            name:Cornelia Trimble
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                  address:
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                     type:PostalAddress
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                  name:Johns Hopkins Medical Institutions
                  address:
                     name:Department of Obstetrics and Gynecology, Johns Hopkins Medical Institutions, Baltimore, USA
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            name:Mei-Cheng Wang
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                  address:
                     name:Department of Biostatistics, Johns Hopkins Medical Institutions, Baltimore, USA
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            name:Chien-Fu Hung
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                  name:The Johns Hopkins University School of Medicine
                  address:
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                     type:PostalAddress
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                     name:Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, USA
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            address:
               name:Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, USA
               type:PostalAddress
            type:Organization
      name:Archana Monie
      affiliation:
            name:The Johns Hopkins University School of Medicine
            address:
               name:Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, USA
               type:PostalAddress
            type:Organization
      name:Ronald D. Alvarez
      affiliation:
            name:University of Alabama at Birmingham
            address:
               name:Department of Obstetrics and Gynecology, University of Alabama at Birmingham, Birmingham, USA
               type:PostalAddress
            type:Organization
      name:Warner K. Huh
      affiliation:
            name:University of Alabama at Birmingham
            address:
               name:Department of Obstetrics and Gynecology, University of Alabama at Birmingham, Birmingham, USA
               type:PostalAddress
            type:Organization
      name:Talia Hoory
      affiliation:
            name:The Johns Hopkins University School of Medicine
            address:
               name:Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, USA
               type:PostalAddress
            type:Organization
      name:Mei-Cheng Wang
      affiliation:
            name:Johns Hopkins Medical Institutions
            address:
               name:Department of Biostatistics, Johns Hopkins Medical Institutions, Baltimore, USA
               type:PostalAddress
            type:Organization
      name:Chien-Fu Hung
      affiliation:
            name:The Johns Hopkins University School of Medicine
            address:
               name:Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, USA
               type:PostalAddress
            type:Organization
            name:Johns Hopkins Medical Institutions
            address:
               name:Department of Oncology, Johns Hopkins Medical Institutions, Baltimore, USA
               type:PostalAddress
            type:Organization
      name:T.-C. Wu
      affiliation:
            name:The Johns Hopkins University School of Medicine
            address:
               name:Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, USA
               type:PostalAddress
            type:Organization
            name:Johns Hopkins Medical Institutions
            address:
               name:Department of Obstetrics and Gynecology, Johns Hopkins Medical Institutions, Baltimore, USA
               type:PostalAddress
            type:Organization
            name:Johns Hopkins Medical Institutions
            address:
               name:Department of Molecular Microbiology and Immunology, Johns Hopkins Medical Institutions, Baltimore, USA
               type:PostalAddress
            type:Organization
            name:Johns Hopkins Medical Institutions
            address:
               name:Department of Oncology, Johns Hopkins Medical Institutions, Baltimore, USA
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, USA
      name:Department of Obstetrics and Gynecology, Chang Gung Memorial Hospital, Kaohsiung Medical Center, Chang Gung University College of Medicine, Kao-hsiung, Taiwan
      name:Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, USA
      name:Department of Obstetrics and Gynecology, Johns Hopkins Medical Institutions, Baltimore, USA
      name:Department of Oncology, Johns Hopkins Medical Institutions, Baltimore, USA
      name:Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, USA
      name:Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, USA
      name:Department of Obstetrics and Gynecology, University of Alabama at Birmingham, Birmingham, USA
      name:Department of Obstetrics and Gynecology, University of Alabama at Birmingham, Birmingham, USA
      name:Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, USA
      name:Department of Biostatistics, Johns Hopkins Medical Institutions, Baltimore, USA
      name:Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, USA
      name:Department of Oncology, Johns Hopkins Medical Institutions, Baltimore, USA
      name:Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, USA
      name:Department of Obstetrics and Gynecology, Johns Hopkins Medical Institutions, Baltimore, USA
      name:Department of Molecular Microbiology and Immunology, Johns Hopkins Medical Institutions, Baltimore, USA
      name:Department of Oncology, Johns Hopkins Medical Institutions, Baltimore, USA
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