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We began analyzing https://www.nature.com/articles/ncomms6283, but it redirected us to https://www.nature.com/articles/ncomms6283. The analysis below is for the second page.

Title[redir]:
Transcriptional specialization of human dendritic cell subsets in response to microbial vaccines | Nature Communications
Description:
The mechanisms by which microbial vaccines interact with human APCs remain elusive. Herein, we describe the transcriptional programs induced in human DCs by pathogens, innate receptor ligands and vaccines. Exposure of DCs to influenza, Salmonella enterica and Staphylococcus aureus allows us to build a modular framework containing 204 transcript clusters. We use this framework to characterize the responses of human monocytes, monocyte-derived DCs and blood DC subsets to 13 vaccines. Different vaccines induce distinct transcriptional programs based on pathogen type, adjuvant formulation and APC targeted. Fluzone, Pneumovax and Gardasil, respectively, activate monocyte-derived DCs, monocytes and CD1c+ blood DCs, highlighting APC specialization in response to vaccines. Finally, the blood signatures from individuals vaccinated with Fluzone or infected with influenza reveal a signature of adaptive immunity activation following vaccination and symptomatic infections, but not asymptomatic infections. These data, offered with a web interface, may guide the development of improved vaccines. The effects of vaccines on human dendritic cells (DCs) are incompletely understood. Here the authors build a transcriptional modular network based on in vitroinfection of human DCs and apply it for the characterization of the DC response to 13 different vaccines.

Matching Content Categories {📚}

  • Science
  • Education
  • Telecommunications

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Custom-built

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🏙️ Massive Traffic: 50M - 100M visitors per month


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Keywords {🔍}

dcs, modules, article, vaccines, response, google, scholar, cas, cells, transcriptional, fig, responses, human, module, data, cdc, monocytes, supplementary, blood, expression, analysis, cell, induced, dendritic, immunity, pathogens, immune, transcripts, individuals, ifn, vaccine, nature, modular, profiles, ifnα, maturation, influenza, vaccination, immunol, framework, apc, fluzone, signatures, time, including, inflammatory, microbial, infection, systems, molecular,

Topics {✒️}

nature portfolio privacy policy granulocyte-macrophage colony-stimulating factor granulocyte/macrophage colony-stimulating factor advertising alexa fluor 700-cd3/cd19/cd20 baylor research institute open questions alexa fluor 700-hla-dr facilitate public access nature 392 nature 466 nature 490 nature 474 nature 0/ reprints research support hla-dr-apc-eflour780 multi-parametric profiles necessitates nucleotide-binding oligomerization domain immunology research research center tumour-necrosis factor α stimulation markers hla-dr computational tools type-ii ifn-related modules single-stranded rna ifn-alpha-producing cd11c social media monocyte-derived dcs remain il-1beta/il-18 processing inflammasome cd4+ t-cell responses directing t-cell responses dendritic cell lineage monocyte-derived inflammatory dcs efficiently cross-present necrotic highlighting cross-platform usability h3n2/wisconsin infection analyses c-type lectin receptors tools systems biology-based characterization activate monocyte-derived dcs highlighting apc-specific responses permissions nf-κb-inducible transcripts /ii ifn-related modules media author correspondence dissect pathogen-induced signatures define pathogen-induced molecular

Schema {🗺️}

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         headline:Transcriptional specialization of human dendritic cell subsets in response to microbial vaccines
         description:The mechanisms by which microbial vaccines interact with human APCs remain elusive. Herein, we describe the transcriptional programs induced in human DCs by pathogens, innate receptor ligands and vaccines. Exposure of DCs to influenza, Salmonella enterica and Staphylococcus aureus allows us to build a modular framework containing 204 transcript clusters. We use this framework to characterize the responses of human monocytes, monocyte-derived DCs and blood DC subsets to 13 vaccines. Different vaccines induce distinct transcriptional programs based on pathogen type, adjuvant formulation and APC targeted. Fluzone, Pneumovax and Gardasil, respectively, activate monocyte-derived DCs, monocytes and CD1c+ blood DCs, highlighting APC specialization in response to vaccines. Finally, the blood signatures from individuals vaccinated with Fluzone or infected with influenza reveal a signature of adaptive immunity activation following vaccination and symptomatic infections, but not asymptomatic infections. These data, offered with a web interface, may guide the development of improved vaccines. The effects of vaccines on human dendritic cells (DCs) are incompletely understood. Here the authors build a transcriptional modular network based on in vitroinfection of human DCs and apply it for the characterization of the DC response to 13 different vaccines.
         datePublished:2014-10-22T00:00:00Z
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      headline:Transcriptional specialization of human dendritic cell subsets in response to microbial vaccines
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