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- John M. Timmerman, MD
- Department of Medicine, Division of Oncology, Stanford University School of Medicine, Stanford, California 94305;
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- Ronald Levy, MD
- Department of Medicine, Division of Oncology, Stanford University School of Medicine, Stanford, California 94305;
抄録
<jats:p>Human tumors express a number of protein antigens that can be recognized by T cells, thus providing potential targets for cancer immunotherapy. Dendritic cells (DCs) are rare leukocytes that are uniquely potent in their ability to present antigens to T cells, and this property has prompted their recent application to therapeutic cancer vaccines. Isolated DCs loaded with tumor antigen ex vivo and administered as a cellular vaccine have been found to induce protective and therapeutic anti-tumor immunity in experimental animals. In pilot clinical trials of DC vaccination for patients with non-Hodgkin's lymphoma and melanoma, induction of anti-tumor immune responses and tumor regressions have been observed. Additional trials of DC vaccination for a variety of human cancers are under way, and methods for targeting tumor antigens to DCs in vivo are also being explored. Exploitation of the antigen-presenting properties of DCs thus offers promise for the development of effective cancer immunotherapies.</jats:p>
収録刊行物
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- Annual Review of Medicine
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Annual Review of Medicine 50 (1), 507-529, 1999-02
Annual Reviews
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詳細情報 詳細情報について
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- CRID
- 1360011145297197056
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- NII論文ID
- 30022132686
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- ISSN
- 1545326X
- 00664219
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- データソース種別
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- Crossref
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