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治疗淋巴增生性疾病的疫苗策略。

Vaccine strategies to treat lymphoproliferative disorders.

作者信息

Radford Kristen J, Vari Frank, Hart Derek N J

机构信息

Mater Medical Research Institute, Dendritic Cell Laboratory, South Brisbane, Queensland, Australia.

出版信息

Pathology. 2005 Dec;37(6):534-50. doi: 10.1080/00313020500376462.

Abstract

Lymphoproliferative disorders, including follicular lymphoma (FL), multiple myeloma (MM) and chronic lymphatic leukaemia (CLL), are slowly progressive malignancies which remain incurable despite advances in therapy. Harnessing the immune system to recognise and destroy tumours is a promising new approach to treating these diseases. Dendritic cells (DC) are unique antigen-presenting cells that play a central role in the initiation and direction of immune responses. DC loaded ex vivo with tumour-associated antigens and administered as a vaccine have already shown promise in early clinical trials for a number of lymphoproliferative disorders, but the need for improvement is widely agreed. Recent advances in the understanding of basic DC biology and lessons from early clinical trials have provided exciting new insights into the generation of anti-tumour immune responses and the design of vaccine strategies. In this review we provide an overview of our current understanding of DC biology and their function in patients with lymphoproliferative disorders. We discuss the current status of clinical trials and new approaches to exploit the antigen presenting capacity of DC to design vaccines of the future.

摘要

包括滤泡性淋巴瘤(FL)、多发性骨髓瘤(MM)和慢性淋巴细胞白血病(CLL)在内的淋巴增殖性疾病是进展缓慢的恶性肿瘤,尽管治疗取得了进展,但仍然无法治愈。利用免疫系统识别和摧毁肿瘤是治疗这些疾病的一种有前景的新方法。树突状细胞(DC)是独特的抗原呈递细胞,在免疫反应的启动和导向中起核心作用。在体外负载肿瘤相关抗原并作为疫苗给药的DC在一些淋巴增殖性疾病的早期临床试验中已显示出前景,但人们普遍认为仍有改进的必要。对基础DC生物学的最新认识进展以及早期临床试验的经验教训为抗肿瘤免疫反应的产生和疫苗策略的设计提供了令人兴奋的新见解。在这篇综述中,我们概述了目前对DC生物学及其在淋巴增殖性疾病患者中的功能的理解。我们讨论了临床试验的现状以及利用DC的抗原呈递能力设计未来疫苗的新方法。

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