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Pathways utilized by dendritic cells for binding, uptake, processing and presentation of antigens derived from HIV-1.

Pathways utilized by dendritic cells for binding, uptake, processing and presentation of antigens derived from HIV-1. Research Abstract Details 

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  • Pathways utilized by dendritic cells for binding, uptake, processing and presentation of antigens derived from HIV-1. Abstract Text:

    rachel l sabadoRachel L Sabado,ethan babcockEthan Babcock,daniel g kavanaghDaniel G Kavanagh,veronica tjomslandVeronica Tjomsland,bruce d walkerBruce D Walker,jeffrey d lifsonJeffrey D Lifson,nina bhardwajNina Bhardwaj,marie larssonMarie Larsson,

    The outcome following HIV infection depends on the nature and durability of the HIV-specific T cell response induced initially. The activation of protective T cell responses depends upon dendritic cells (DC), antigen-presenting cells which have the capacity to process and present viral antigens. DC pulsed with aldrithiol-2-inactivated HIV and delivered in vivo were reported to induce immune responses and promote virologic control in chronically HIV-1-infected subjects. To gain an understanding of this phenomenon, we characterized the steps involved in the presentation of antigens derived from aldrithiol-2-treated vs. infectious HIV-1 by DC. Antigen presentation, on both MHC class I and II, was independent of DC-specific ICAM-3-grabbing integrin, DEC-205 and macrophage mannose receptor, C-type lectins expressed by the DC. Inhibitor studies showed that presentation on MHC class I was dependent on viral fusion in a CD4/coreceptor-dependent manner, both at the cell surface and within endosomes, and access to the classical endosomal processing pathway. MHC class II presentation of HIV-associated antigens was dependent on active endocytosis, probably receptor-mediated, and subsequent degradation of virions in acidified endosomes in the DC. Our study brings forth new facts regarding the binding, uptake, and processing of chemically inactivated virions leading to efficient antigen presentation and should aid in the design of more effective HIV vaccines.

    Pathways utilized by dendritic cells for binding, uptake, processing and presentation of antigens derived from HIV-1. Publishing Authors By Initials

    rl sabadoRL Sabado,e babcockE Babcock,dg kavanaghDG Kavanagh,v tjomslandV Tjomsland,bd walkerBD Walker,jd lifsonJD Lifson,n bhardwajN Bhardwaj,m larssonM Larsson,

    For similar viruses: virion research abstracts see: viruses: virion research

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    MEDLINE DATE:

    Pathways utilized by dendritic cells for binding, uptake, processing and presentation of antigens derived from HIV-1. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: European journal of immunology

    VOLUME: 37

    Page Numbers: 1752-63

    Journal Abbreviation: Eur. J. Immunol.

    ISSN: 0014-2980

    DAY: 3

    MONTH: Jul

    YEAR: 2007

    Pathways utilized by dendritic cells for binding, uptake, processing and presentation of antigens derived from HIV-1. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 1273201

    Pathways utilized by dendritic cells for binding, uptake, processing and presentation of antigens derived from HIV-1. Keywords Mesh Terms:

    KEYWORDS: Virion

    MESH TERMS: immunology

    Chemical & Substance for Abstract: Pathways utilized by dendritic cells for binding, uptake, processing and presentation of antigens derived from HIV-1. Information

    Substance Name: 2,2'-Dipyridyl

    Registry Number: 366-18-7

    Grant and Affiliation Information for Pathways utilized by dendritic cells for binding, uptake, processing and presentation of antigens derived from HIV-1.

    AFFILIATION: Department of Medicine and Pathology, School of Medicine, New York University, NY, USA.

    Country: Germany

    Germany Research PublicationGermany Research Publication

    AGENCY: United States NCI

    GRANT: N01 CO12400

    ACRONYM: CO

    MEDLINETA: Eur J Immunol

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

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