Literature DB >> 21488899

Dendritic cell control of tolerogenic responses.

Santhakumar Manicassamy1, Bali Pulendran.   

Abstract

One of the most fundamental problems in immunology is the seemingly schizophrenic ability of the immune system to launch robust immunity against pathogens, while acquiring and maintaining a state of tolerance to the body's own tissues and the trillions of commensal microorganisms and food antigens that confront it every day. A fundamental role for the innate immune system, particularly dendritic cells (DCs), in orchestrating immunological tolerance has been appreciated, but emerging studies have highlighted the nature of the innate receptors and the signaling pathways that program DCs to a tolerogenic state. Furthermore, several studies have emphasized the major role played by cellular interactions and the microenvironment in programming tolerogenic DCs. Here, we review these studies and suggest that the innate control of tolerogenic responses can be viewed as different hierarchies of organization, in which DCs, their innate receptors and signaling networks, and their interactions with other cells and local microenvironments represent different levels of the hierarchy.
© 2011 John Wiley & Sons A/S.

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Year:  2011        PMID: 21488899      PMCID: PMC3094730          DOI: 10.1111/j.1600-065X.2011.01015.x

Source DB:  PubMed          Journal:  Immunol Rev        ISSN: 0105-2896            Impact factor:   12.988


  296 in total

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Journal:  Immunity       Date:  2005-04       Impact factor: 31.745

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9.  Fc gamma RIIB regulates nasal and oral tolerance: a role for dendritic cells.

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Review 6.  Clinical view on the importance of dendritic cells in asthma.

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7.  Activation of GILZ gene by photoactivated 8-methoxypsoralen: potential role of immunoregulatory dendritic cells in extracorporeal photochemotherapy.

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8.  Lymph Node Stromal Fiber ER-TR7 Modulates CD4+ T Cell Lymph Node Trafficking and Transplant Tolerance.

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10.  Reprogramming the Local Lymph Node Microenvironment Promotes Tolerance that Is Systemic and Antigen Specific.

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