Novel Immunotherapies

被引:19
作者
Yi, Qing [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Lymphoma & Myeloma, Div Canc Med, Ctr Canc Immunol Res,Unit 0903, Houston, TX 77030 USA
关键词
multiple myeloma; immunotherapy; tumor antigens; antibodies; T cells; CYTOTOXIC-T-LYMPHOCYTES; MULTIPLE-MYELOMA PATIENTS; BONE-MARROW-TRANSPLANTATION; ANTI-BETA(2)-MICROGLOBULIN MONOCLONAL-ANTIBODIES; DENDRITIC CELL VACCINATION; COLONY-STIMULATING FACTOR; MALIGNANT PLASMA-CELLS; IDIOTYPE VACCINATION; SPERM PROTEIN-17; SERUM BETA-2-MICROGLOBULIN;
D O I
10.1097/PPO.0b013e3181c51f0d
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Multiple myeloma is still a fatal disease. Despite advances in high-dose chemotherapy and stein-cell transplantation and the development of novel therapeutics, relapse of the underlying disease remains the primary cause of treatment failure. Strategies for posttransplantation immunomodulation are desirable for eradication of remaining tumor cells. To this end, immunotherapy aimed at inducing myeloma-specific immunity in patients has been explored. Idiotype protein, secreted by myeloma cells, has been the primary target for immunotherapy as it is the best defined tumor-specific antigen. This chapter focuses on novel immunotherapies that are being developed to treat patients with myeloma, I will discuss potential myeloma antigens, anti gen-specific T cells, and their function on myeloma tumor cells, and T-cell-based and antibody-based immunotherapies for myeloma. Furthermore, clinical studies of T-cell-based immunotherapy in the form of vaccination, allogencic stein-cell transplantation and donor lymphocyte infusions, with or without donor vaccination using patient-derived idiotype, and future application of donor-derived or patient-derived, anti gen-specific T-cell infusion in this disease are also discussed. Based on the specificity of the immune effector molecules and cells, immunotherapies with specific T cells or therapeutic antibodies may represent novel strategies for the treatment of multiple myeloma in the near future.
引用
收藏
页码:502 / 510
页数:9
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