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用于肾细胞癌的树突状细胞-肿瘤融合疫苗

Dendritic cell-tumor fusion vaccines for renal cell carcinoma.

作者信息

Avigan David

机构信息

Beth Israel Deaconess Medical Center, Boston, Massachusetts 02215, USA.

出版信息

Clin Cancer Res. 2004 Sep 15;10(18 Pt 2):6347S-52S. doi: 10.1158/1078-0432.CCR-050005.

Abstract

Renal cell carcinoma is a malignant disease that demonstrates resistance to standard chemotherapeutic agents. A promising area of investigation is the use of cancer vaccines to educate host immunity to specifically target and eliminate malignant cells. Dendritic cells (DCs) are potent antigen-presenting cells that are uniquely effective in generating primary immune responses. DCs that are manipulated to present tumor antigens induce antitumor immunity in animal models and preclinical human studies. A myriad of strategies have been developed to effectively load tumor antigen onto DCs, including the introduction of individual peptides, proteins, or tumor-specific genes, as well as the use of whole tumor cells as a source of antigen. A promising approach for the design of cancer vaccines involves the fusion of whole tumor cells with DCs. The DC-tumor fusion presents a spectrum of tumor-associated antigens to helper and cytotoxic T-cell populations in the context of DC-mediated costimulatory signals. In animal models, vaccination with DC-tumor fusions resulted in protection from tumor challenge and regression of established metastatic disease. We have conducted phase 1 dose escalation studies in which patients with metastatic breast and renal cancer underwent vaccination with DC-tumor fusions. Twenty-three patients underwent vaccination with autologous DC-tumor fusions. Vaccination was well tolerated without substantial treatment-related toxic effects. Immunologic responses and disease regression were observed in a subset of patients. Future studies will explore the effect of DC maturation and cytokine adjuvants on vaccine potency.

摘要

肾细胞癌是一种对标准化疗药物具有抗性的恶性疾病。一个有前景的研究领域是使用癌症疫苗来激发宿主免疫,以特异性地靶向并消除恶性细胞。树突状细胞(DCs)是强大的抗原呈递细胞,在产生初级免疫反应方面具有独特的有效性。经操控以呈递肿瘤抗原的DCs在动物模型和临床前人体研究中可诱导抗肿瘤免疫。已经开发出无数种策略来有效地将肿瘤抗原加载到DCs上,包括引入单个肽、蛋白质或肿瘤特异性基因,以及使用全肿瘤细胞作为抗原来源。一种有前景的癌症疫苗设计方法涉及将全肿瘤细胞与DCs融合。DC-肿瘤融合物在DC介导的共刺激信号的背景下,向辅助性T细胞群体和细胞毒性T细胞群体呈递一系列肿瘤相关抗原。在动物模型中,用DC-肿瘤融合物进行疫苗接种可使动物免受肿瘤攻击,并使已形成的转移性疾病消退。我们已经进行了1期剂量递增研究,转移性乳腺癌和肾细胞癌患者接受了DC-肿瘤融合物疫苗接种。23名患者接受了自体DC-肿瘤融合物疫苗接种。疫苗接种耐受性良好,没有明显的与治疗相关的毒性作用。在一部分患者中观察到了免疫反应和疾病消退。未来的研究将探索DC成熟和细胞因子佐剂对疫苗效力的影响。

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