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      Rational Design of Pathogen-Mimicking Amphiphilic Materials as Nanoadjuvants

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          Abstract

          An opportunity exists today for cross-cutting research utilizing advances in materials science, immunology, microbial pathogenesis, and computational analysis to effectively design the next generation of adjuvants and vaccines. This study integrates these advances into a bottom-up approach for the molecular design of nanoadjuvants capable of mimicking the immune response induced by a natural infection but without the toxic side effects. Biodegradable amphiphilic polyanhydrides possess the unique ability to mimic pathogens and pathogen associated molecular patterns with respect to persisting within and activating immune cells, respectively. The molecular properties responsible for the pathogen-mimicking abilities of these materials have been identified. The value of using polyanhydride nanovaccines was demonstrated by the induction of long-lived protection against a lethal challenge of Yersinia pestis following a single administration ten months earlier. This approach has the tantalizing potential to catalyze the development of next generation vaccines against diseases caused by emerging and re-emerging pathogens.

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          Most cited references27

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          Natural adjuvants: endogenous activators of dendritic cells.

          Dendritic cells, the most potent antigen-presenting cells, need to be activated before they can function to initiate an immune response. We report here that, in the absence of any foreign substances, dendritic cells can be activated by endogenous signals received from cells that are stressed, virally infected or killed necrotically, but not by healthy cells or those dying apoptotically. Injected in vivo with an antigen, the endogenous activating substances can function as natural adjuvants to stimulate a primary immune response, and they may represent the natural initiators of transplant rejection, spontaneous tumor rejection, and some forms of autoimmunity.
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            Bacterial manipulation of innate immunity to promote infection.

            The mammalian innate immune response provides a barrier against invading pathogens. Innate immune mechanisms are used by the host to respond to a range of bacterial pathogens in an acute and conserved fashion. Host cells express pattern recognition receptors that sense pathogen-associated molecular patterns. After detection, an arsenal of antimicrobial mechanisms is deployed to kill bacteria in infected cells. Innate immunity also stimulates antigen-specific responses mediated by the adaptive immune system. In response, pathogens manipulate host defence mechanisms to survive and eventually replicate. This Review focuses on the control of host innate immune responses by pathogenic intracellular bacteria.
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              Structure and function of lipopolysaccharides.

              The lipopolysaccharides of Gram-negative bacteria have a profound effect on the mammalian immune system and are of great significance in the pathophysiology of many disease processes. Consideration is given in this review to the relationship between structure and function of these lipopolysaccharides.
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                Author and article information

                Journal
                Sci Rep
                Scientific Reports
                Nature Publishing Group
                2045-2322
                16 December 2011
                2011
                : 1
                : 198
                Affiliations
                [1 ]simpleDepartment of Chemical and Biological Engineering, Iowa State University , Ames, IA 50011
                [2 ]simpleDepartment of Veterinary Microbiology and Preventive Medicine, Iowa State University , Ames, IA 50011
                [3 ]simpleDepartment of Materials Science and Engineering, Iowa State University , Ames, IA 50011
                [4 ]simpleCenter for Immunology and Microbial Disease, Albany Medical College , Albany, NY 12208
                [5 ]These authors contributed equally to this work.
                Author notes
                Article
                srep00198
                10.1038/srep00198
                3240970
                22355713
                6d480137-22d2-4e4a-ae3d-a9999ada5633
                Copyright © 2011, Macmillan Publishers Limited. All rights reserved

                This work is licensed under a Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/

                History
                : 20 July 2011
                : 24 November 2011
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