抗原
树突状细胞
医学
免疫系统
离体
免疫学
癌症
免疫疗法
前列腺癌
抗原呈递
抗原提呈细胞
肿瘤抗原
癌症研究
T细胞
体内
生物
内科学
生物技术
作者
Frank H. Valone,Eric J. Small,Malcolm R. MacKenzie,Patrick Burch,Martha Q. Lacy,Madhusudan V. Peshwa,Reiner Laus
出处
期刊:PubMed
日期:2002-01-05
卷期号:7 Suppl 2: S53-61
被引量:17
摘要
Dendritic cells are the most potent antigen-presenting cells and are critical to initiation of immune responses. Dendritic cells loaded ex vivo with tumor-associated antigen are being administered to cancer patients in an effort to jump-start a potent, cell-mediated anticancer immune response resulting in tumor shrinkage and clinical benefit.Dendreon Corporation has designed three therapeutic vaccines using blood-derived dendritic cells loaded ex vivo with antigen: Provenge for prostate cancer; Mylovenge for multiple myeloma and other B-cell malignancies; and APC8024 for cancers expressing the HER-2/neu proto-oncogene.Preclinical studies demonstrated that blood dendritic cells matured spontaneously in short-term culture without growth factors, and that fusion of antigens with granulocyte-macrophage colony-stimulating factor enhances antigen uptake and presentation by blood dendritic cells. Phase I/II trials suggest that these dendritic cell-based vaccines are safe and well tolerated. Provenge has demonstrated antitumor activity in hormone-refractory prostate cancer; approximately 20% of patients experienced decreased prostate-specific antigen (i.e., PSA) levels and a similar percentage experienced disease stabilization. Double-blind, placebo-controlled, randomized trials in metastatic, asymptomatic hormone-refractory prostate cancer have been initiated. Phase II data on Mylovenge are similarly encouraging, and expanded phase II testing is ongoing in anticipation of opening phase III trials in 2002. APC8024 is in early clinical development and has shown significant capacity to elicit antigen-specific immune responses.Antigen delivery by ex vivo antigen-loaded dendritic cells may be an effective approach to cancer immunotherapy.
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