We are analyzing https://link.springer.com/chapter/10.1007/978-0-387-34814-8_14.

Title:
CD4+ T Cells Cooperate With Macrophages for Specific Elimination of MHC Class II-Negative Cancer Cells | SpringerLink
Description:
Our present knowledge of how T cells eliminate cancer is mainly based on memory immune responses investigated with vaccinated mice1,2. In-vivo depletion studies with anti-CD4 monoclonal antibodies (mAb) have revealed that the antitumor immunity conferred by...
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Topics {✒️}

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Schema {🗺️}

ScholarlyArticle:
      headline:CD4+ T Cells Cooperate With Macrophages for Specific Elimination of MHC Class II-Negative Cancer Cells
      pageEnd:208
      pageStart:195
      image:https://media.springernature.com/w153/springer-static/cover/book/978-0-387-34814-8.jpg
      genre:
         Biomedical and Life Sciences
         Biomedical and Life Sciences (R0)
      isPartOf:
         name:Crossroads between Innate and Adaptive Immunity
         isbn:
            978-0-387-34814-8
            978-0-387-34813-1
         type:Book
      publisher:
         name:Springer US
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:Alexandre Corthay
            affiliation:
                  name:University of Oslo and Rikshospitalet-Radiumhospitalet Medical Center
                  address:
                     name:Institute of Immunology, University of Oslo and Rikshospitalet-Radiumhospitalet Medical Center, Oslo, Norway
                     type:PostalAddress
                  type:Organization
            type:Person
      keywords:Myeloma Cell, SCID Mouse, Antitumor Immunity, Tumor Rejection, Tumor Eradication
      description:Our present knowledge of how T cells eliminate cancer is mainly based on memory immune responses investigated with vaccinated mice1,2. In-vivo depletion studies with anti-CD4 monoclonal antibodies (mAb) have revealed that the antitumor immunity conferred by prophylactic vaccination is usually CD4+ T cell dependent. CD4+ T cells were required for vaccination-induced immunity against the B16 melanoma3–5, against the Mc51.9 fibrosarcoma6, against the J558 plasmacytoma7, and against the A20 lymphoma7.
      datePublished:2007
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Book:
      name:Crossroads between Innate and Adaptive Immunity
      isbn:
         978-0-387-34814-8
         978-0-387-34813-1
Organization:
      name:Springer US
      logo:
         url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
         type:ImageObject
      name:University of Oslo and Rikshospitalet-Radiumhospitalet Medical Center
      address:
         name:Institute of Immunology, University of Oslo and Rikshospitalet-Radiumhospitalet Medical Center, Oslo, Norway
         type:PostalAddress
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      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:Alexandre Corthay
      affiliation:
            name:University of Oslo and Rikshospitalet-Radiumhospitalet Medical Center
            address:
               name:Institute of Immunology, University of Oslo and Rikshospitalet-Radiumhospitalet Medical Center, Oslo, Norway
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Institute of Immunology, University of Oslo and Rikshospitalet-Radiumhospitalet Medical Center, Oslo, Norway
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