Literature DB >> 21029958

Designing vaccines based on biology of human dendritic cell subsets.

Karolina Palucka1, Jacques Banchereau, Ira Mellman.   

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.
Copyright © 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 21029958      PMCID: PMC2975953          DOI: 10.1016/j.immuni.2010.10.007

Source DB:  PubMed          Journal:  Immunity        ISSN: 1074-7613            Impact factor:   31.745


  144 in total

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Review 6.  Differentiation and function of mouse monocyte-derived dendritic cells in steady state and inflammation.

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Review 8.  Harnessing human dendritic cell subsets for medicine.

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  123 in total

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7.  Targeting of human antigen-presenting cell subsets.

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Review 8.  The role of dendritic cells in driving genital tract inflammation and HIV transmission risk: are there opportunities to intervene?

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Review 9.  Engineering better immunotherapies via RNA interference.

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10.  Role of fatty-acid synthesis in dendritic cell generation and function.

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