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Genetic redirection of T cells for cancer therapy

期刊

JOURNAL OF LEUKOCYTE BIOLOGY
卷 87, 期 5, 页码 791-803

出版社

FEDERATION AMER SOC EXP BIOL
DOI: 10.1189/jlb.1209824

关键词

adoptive immunotherapy; chimeric receptor; tumor; retroviral vector; lentiviral vector; TCR

资金

  1. National Health and Medical Research Council of Australia (NHMRC)
  2. Cancer Council of Victoria
  3. Susan G. Komen Breast Cancer Foundation
  4. Bob Parker Memorial Trust
  5. Peter MacCallum Cancer Centre Foundation

向作者/读者索取更多资源

Adoptive immunotherapy can induce dramatic tumor regressions in patients with melanoma or viral-induced malignancies, but extending this approach to many common cancers has been hampered by a lack of naturally occurring tumor-specific T cells. In this review, we describe recent advances in the genetic modification of T cells using genes encoding cell-surface receptors specific for tumor-associated antigen. Using genetic modification, the many functional properties of T cells, including cytokine secretion and cytolytic capacity, are redirected from their endogenous specificity toward the elimination of tumor cells. Advances in gene design, vectors, and cell production are discussed, and details of the progress in clinical application of this approach are provided. J. Leukoc. Biol. 87: 791-803; 2010.

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