Tumor Rejection After Direct Costimulation of CD8 <sup>+</sup> T Cells by B7-Transfected Melanoma Cells
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- Sarah E. Townsend
- Department of Molecular and Cell Biology and Cancer Research Laboratory, University of California, Berkeley, CA 94720.
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- James P. Allison
- Department of Molecular and Cell Biology and Cancer Research Laboratory, University of California, Berkeley, CA 94720.
抄録
<jats:p> A variety of tumors are potentially immunogenic but do not stimulate an effective anti-tumor immune response in vivo. Tumors may be capable of delivering antigen-specific signals to T cells, but may not deliver the costimulatory signals necessary for full activation of T cells. Expression of the costimulatory ligand B7 on melanoma cells was found to induce the rejection of a murine melanoma in vivo. This rejection was mediated by CD8 <jats:sup>+</jats:sup> T cells; CD4 <jats:sup>+</jats:sup> T cells were not required. These results suggest that B7 expression renders tumor cells capable of effective antigen presentation, leading to their eradication in vivo. </jats:p>
収録刊行物
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- Science
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Science 259 (5093), 368-370, 1993-01-15
American Association for the Advancement of Science (AAAS)
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詳細情報 詳細情報について
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- CRID
- 1363670319678407808
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- NII論文ID
- 80006884937
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- ISSN
- 10959203
- 00368075
- http://id.crossref.org/issn/00368075
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