About: The interaction of HIV with dendritic cells: outcomes and pathways

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An Entity of Type : schema:ScholarlyArticle, within Data Space : covidontheweb.inria.fr associated with source document(s)

Attributes	Values
type	Academic Article research paper schema:ScholarlyArticle
isDefinedBy	Covid-on-the-Web dataset
has title	The interaction of HIV with dendritic cells: outcomes and pathways
Creator	Piguet, Vincent Steinman, Ralph
Source	Elsevier; Medline; PMC
abstract	Dendritic cells (DCs), including Langerhans Cells (LCs), are probably among the earliest targets of HIV infection. Their localization in mucosal epithelia and in the T cell areas of lymphoid organs, as well as their crucial role in capturing antigens and initiating T cell responses, highlight their potential importance. Studies with cells in culture have addressed different outcomes of the HIV-–DC interaction, which include: direct productive infection of DC; carriage of virus by DC to CD4(+) T cells; transfer of virus between DC and T cells at an infectious synapse; and immune evasion strategies of infected DC. Here we review the literature covering these areas, including current knowledge of underlying mechanisms or pathways.
has issue date	2007-10-23(xsd:dateTime)
bibo:doi	10.1016/j.it.2007.07.010
bibo:pmid	17950666
has license	no-cc
sha1sum (hex)	c3bbc7f82a0f5cda07bf1cfd9d7951b0156e5b1f
schema:url	https://doi.org/10.1016/j.it.2007.07.010
resource representing a document's title	The interaction of HIV with dendritic cells: outcomes and pathways
has PubMed Central identifier	PMC7106400
has PubMed identifier	17950666
schema:publication	Trends Immunol
resource representing a document's body	covid:c3bbc7f82a0f5cda07bf1cfd9d7951b0156e5b1f#body_text
is schema:about of	named entity 'dendritic cells' named entity 'APOBEC' named entity 'DCs' named entity 'CD4 +' named entity 'CXCR4' named entity 'synapse' named entity 'DCs' named entity 'HIV' named entity 'Birbeck' named entity 'DC-SIGN' named entity 'immune responses' named entity 'cytokines' named entity 'lymph nodes' named entity 'vagina' named entity 'HIV' named entity 'APOBEC3G' named entity 'HIV' named entity 'retrotransposons' named entity 'chemokine' named entity 'Langerin' named entity 'virus' named entity 'simple explanation' named entity 'adaptive immunity' named entity 'DC-SIGN' named entity 'recycling endosomes' named entity 'SIV' named entity 'T-cell' named entity 'viruses' named entity 'TGF-b' named entity 'tetraspanins' named entity 'DCs' named entity 'DC-SIGN' named entity 'dermal' named entity 'CD4 +' named entity 'CCR5' named entity 'DCs' named entity 'DCs' named entity 'HIV' named entity 'DCs' named entity 'DCs' named entity 'HIV infection' named entity 'C-type lectin' named entity 'HIV infection' named entity 'lymphocytes' named entity 'HIV' named entity 'DCs' named entity 'CD34' named entity 'vagina' named entity 'HIV' named entity 'DC-SIGN' named entity 'CD4 +' named entity 'viral protein' named entity 'infection' named entity 'endosomes' named entity 'virus' named entity 'HIV' named entity 'HIV' named entity 'DCs' named entity 'DCs' named entity 'monocytes' named entity 'HIV' named entity 'immunological synapse' named entity 'HIV infection' named entity 'lymphoid tissue' named entity 'DCs' named entity 'DCs' named entity 'squamous epithelium' named entity 'coronavirus' named entity 'tumors' named entity 'DCs' named entity 'DCs' named entity 'viruses' named entity 'DCs' named entity 'ICAM-3' named entity 'epithelia' named entity 'HIV infection' named entity 'vaginal epithelium' named entity 'DCs' named entity 'CCR5' named entity 'APOBEC'

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