An Update on Malignant Melanoma Vaccine ResearchInsights into Mechanisms for Improving the Design and Potency of Melanoma Therapeutic Vaccines

被引:0
作者
Stephen John Ralph
机构
[1] Griffith University,School of Medical Science
来源
American Journal of Clinical Dermatology | 2007年 / 8卷
关键词
Melanoma; Melanoma Cell; Metastatic Melanoma; Ipilimumab; Cancer Vaccine;
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摘要
Currently, cancer vaccine therapy for melanoma has a 2-fold focus. On the one hand, advances have been aimed at improving the effectiveness of melanoma vaccines based on a greater understanding of melanoma tumor cell biology. On the other hand, there is increasing evidence that the immune system, our defense against tumors, also inadvertently plays a supportive role in promoting the development and progression of tumors. Hence, two opposing forces ‘hanging in the balance’ dictate patients’ responses to melanoma: tumor cell biology and the status of the immune system. Recent developments in our understanding of both of these aspects have provided new leads and insights for novel ways to improve vaccine design and add to the melanoma vaccine armory. As the focus of immunotherapy shifts its aim towards the tumor microenvironment, we are now developing the ability to program the immune responses raised by vaccination against melanoma. The aim here is to prevent myeloid and regulatory T-cell-mediated immune suppression as well as to counteract tumor-derived factors capable of suppressing immune responses. A redirected strategy for vaccine immunotherapy is proposed based on our greater understanding of tumor immunity. Using a combination therapy of immune-potentiating melanoma vaccines together with adjuvants for overcoming the immunosuppressive forces will allow us to activate protective immunity against melanoma. Other cancer vaccines (i.e. colon or renal) are already offering reasons for hope and expectation that vaccine immunotherapy will also produce successful outcomes for patients with melanoma.
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页码:123 / 141
页数:18
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  • [81] Davies H(2001)CDKN2A and CDK4 mutation analysis in Italian melanoma-prone families: functional characterization of a novel CDKN2A germ line mutation Br J Cancer 85 836-300
  • [82] Bignell GR(2005)Prevalence of 9p21 deletions in UK melanoma families Genes Chromosomes Cancer 44 292-43
  • [83] Cox C(1992)Mapping of the shortest region of overlap of deletions of the short arm of chromosome 9 associated with human neoplasia Genomics 14 437-52
  • [84] Brose MS(1994)Structure of the human type-I interferon gene cluster determined from a YAC clone contig Genomics 22 540-23
  • [85] Volpe P(1999)The prognostic significance of altered cyclin-dependent kinase inhibitors in human cancer Annu Rev Med 50 401-6
  • [86] Feldman M(1999)Sensitivity to extrinsically supplied interferon and the endogenous expression of interferon in melanoma cell lines Melanoma Res 9 451-9
  • [87] Pollock PM(1992)Correlation between interferon (IFN) alpha resistance and deletion of the IFN alpha/beta genes in acute leukemia cell lines suggests selection against the IFN system Blood 80 744-25
  • [88] Meltzer PS(1983)Effects of cloned human leukocyte interferons in the human tumor stem cell assay J Clin Oncol 1 217-25
  • [89] Satyamoorthy K(1986)Antiproliferative effects of interferons on human melanoma cells in the human tumor colony-forming assay J Interferon Res 6 615-25
  • [90] Li G(1984)Human tumor colony assay and chemosensitivity testing Cancer Treat Rep 68 117-8