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Title:
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.
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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.
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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.
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type:Organization
name:Derek Blankenship
affiliation:
name:Baylor Institute for Immunology Research
address:
name:Baylor Institute for Immunology Research, Dallas, USA
type:PostalAddress
type:Organization
name:Sangkon Oh
affiliation:
name:Baylor Institute for Immunology Research
address:
name:Baylor Institute for Immunology Research, Dallas, USA
type:PostalAddress
type:Organization
name:Octavio Ramilo
affiliation:
name:Nationwide Childrenâs Hospital
address:
name:Nationwide Childrenâs Hospital, Columbus, USA
type:PostalAddress
type:Organization
name:Damien Chaussabel
affiliation:
name:Benaroya Research Institute
address:
name:Benaroya Research Institute, Seattle, USA
type:PostalAddress
type:Organization
name:Sidra Medical and Research Center
address:
name:Sidra Medical and Research Center, Qatar
type:PostalAddress
type:Organization
name:Jacques Banchereau
affiliation:
name:Baylor Institute for Immunology Research
address:
name:Baylor Institute for Immunology Research, Dallas, USA
type:PostalAddress
type:Organization
name:Jackson Laboratory for Genomic Medicine
address:
name:Jackson Laboratory for Genomic Medicine, Farmington, USA
type:PostalAddress
type:Organization
name:Karolina Palucka
affiliation:
name:Baylor Institute for Immunology Research
address:
name:Baylor Institute for Immunology Research, Dallas, USA
type:PostalAddress
type:Organization
name:Jackson Laboratory for Genomic Medicine
address:
name:Jackson Laboratory for Genomic Medicine, Farmington, USA
type:PostalAddress
type:Organization
name:Virginia Pascual
affiliation:
name:Baylor Institute for Immunology Research
address:
name:Baylor Institute for Immunology Research, Dallas, USA
type:PostalAddress
type:Organization
email:[email protected]
PostalAddress:
name:Baylor Institute for Immunology Research, Dallas, USA
name:Baylor Institute for Immunology Research, Dallas, USA
name:Baylor Institute for Immunology Research, Dallas, USA
name:Baylor Institute for Immunology Research, Dallas, USA
name:Baylor Institute for Immunology Research, Dallas, USA
name:Baylor Institute for Immunology Research, Dallas, USA
name:Baylor Institute for Immunology Research, Dallas, USA
name:Baylor Institute for Immunology Research, Dallas, USA
name:Baylor Institute for Immunology Research, Dallas, USA
name:Baylor Institute for Immunology Research, Dallas, USA
name:Baylor Institute for Immunology Research, Dallas, USA
name:Baylor Institute for Immunology Research, Dallas, USA
name:Baylor Institute for Immunology Research, Dallas, USA
name:Baylor Institute for Immunology Research, Dallas, USA
name:Baylor Institute for Immunology Research, Dallas, USA
name:Baylor Institute for Immunology Research, Dallas, USA
name:Baylor Institute for Immunology Research, Dallas, USA
name:Nationwide Childrenâs Hospital, Columbus, USA
name:Benaroya Research Institute, Seattle, USA
name:Sidra Medical and Research Center, Qatar
name:Baylor Institute for Immunology Research, Dallas, USA
name:Jackson Laboratory for Genomic Medicine, Farmington, USA
name:Baylor Institute for Immunology Research, Dallas, USA
name:Jackson Laboratory for Genomic Medicine, Farmington, USA
name:Baylor Institute for Immunology Research, Dallas, USA
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