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基于人类树突状细胞亚群生物学设计疫苗。

Designing vaccines based on biology of human dendritic cell subsets.

机构信息

Baylor Institute for Immunology Research, 3434 Live Oak Avenue, Dallas, TX 75204, USA.

出版信息

Immunity. 2010 Oct 29;33(4):464-78. doi: 10.1016/j.immuni.2010.10.007.

Abstract

The effective vaccines developed against a variety of infectious agents, including polio, measles, and hepatitis B, represent major achievements in medicine. These vaccines, usually composed of microbial antigens, are often associated with an adjuvant that activates dendritic cells (DCs). Many infectious diseases are still in need of an effective vaccine including HIV, malaria, hepatitis C, and tuberculosis. In some cases, the induction of cellular rather than humoral responses may be more important because the goal is to control and eliminate the existing infection rather than to prevent it. Our increased understanding of the mechanisms of antigen presentation, particularly with the description of DC subsets with distinct functions, as well as their plasticity in responding to extrinsic signals, represent opportunities to develop novel vaccines. In addition, we foresee that this increased knowledge will permit us to design vaccines that will reprogram the immune system to intervene therapeutically in cancer, allergy, and autoimmunity.

摘要

针对多种传染病病原体(包括脊髓灰质炎、麻疹和乙型肝炎)开发的有效疫苗是医学上的重大成就。这些疫苗通常由微生物抗原组成,常与佐剂联合使用,佐剂可激活树突状细胞(DC)。许多传染病仍需要有效的疫苗,包括 HIV、疟疾、丙型肝炎和结核病。在某些情况下,诱导细胞而非体液反应可能更为重要,因为目标是控制和消除现有的感染,而不是预防感染。我们对抗原呈递机制的认识不断加深,特别是描述了具有不同功能的 DC 亚群及其对外部信号的可塑性,这为开发新型疫苗提供了机会。此外,我们预计,这方面知识的增加将使我们能够设计疫苗,重新编程免疫系统,在癌症、过敏和自身免疫方面进行治疗干预。

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