J
Jun Wang
Researcher at Science for Life Laboratory
Publications - 9
Citations - 1355
Jun Wang is an academic researcher from Science for Life Laboratory. The author has contributed to research in topics: Immune system & Internal medicine. The author has an hindex of 6, co-authored 7 publications receiving 436 citations.
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Journal ArticleDOI
The Immunology of Multisystem Inflammatory Syndrome in Children with COVID-19
Camila Rosat Consiglio,Nicola Cotugno,Nicola Cotugno,Fabian Sardh,Christian Pou,Donato Amodio,Donato Amodio,Lucie Rodriguez,Ziyang Tan,Sonia Zicari,Alessandra Ruggiero,Giuseppe Rubens Pascucci,Veronica Santilli,Tessa M. Campbell,Yenan T. Bryceson,Daniel Eriksson,Daniel Eriksson,Jun Wang,Alessandra Marchesi,Tadepally Lakshmikanth,Andrea Campana,Alberto Villani,Paolo Rossi,Paolo Rossi,Nils Landegren,Nils Landegren,Paolo Palma,Paolo Palma,Petter Brodin,Petter Brodin +29 more
TL;DR: The inflammatory response in MIS-C differs from the cytokine storm of severe acute COVID-19, shares several features with Kawasaki disease, but also differs from this condition with respect to T cell subsets, interleukin (IL)-17A, and biomarkers associated with arterial damage.
Posted ContentDOI
The Immunology of Multisystem Inflammatory Syndrome in Children with COVID-19
Camila Rosat Consiglio,Nicola Cotugno,Nicola Cotugno,Fabian Sardh,Christian Pou,Donato Amodio,Donato Amodio,Lucie Rodriguez,Ziyang Tan,Sonia Zicari,Alessandra Ruggiero,Giuseppe Rubens Pascucci,Veronica Santilli,Tessa M. Campbell,Yenan T. Bryceson,Daniel Eriksson,Daniel Eriksson,Jun Wang,Alessandra Marchesi,Tadepally Lakshmikanth,Andrea Campana,Alberto Villani,Paolo Rossi,Paolo Rossi,Nils Landegren,Nils Landegren,Paolo Palma,Paolo Palma,Petter Brodin,Petter Brodin +29 more
TL;DR: The inflammatory response in MIS-C differs from the cytokine storm of severe acute COVID-19, is more similar to Kawasaki disease, but also differ from this with respect to T-cell subsets, IL-17A and biomarkers associated with arterial damage.
Journal ArticleDOI
Bifidobacteria-mediated immune system imprinting early in life.
Bethany M. Henrick,Lucie Rodriguez,Tadepally Lakshmikanth,Christian Pou,Ewa Henckel,Ewa Henckel,Ewa Henckel,Aron Arzoomand,Axel Olin,Jun Wang,Jaromír Mikeš,Ziyang Tan,Yang Chen,Amy M. Ehrlich,Anna Karin Bernhardsson,Constantin Habimana Mugabo,Ylva Ambrosiani,Anna Gustafsson,Anna Gustafsson,Stephanie Chew,Heather Brown,Johann Prambs,Kajsa Bohlin,Kajsa Bohlin,Ryan D. Mitchell,Mark A. Underwood,Jennifer T. Smilowitz,J. Bruce German,Steven A. Frese,Steven A. Frese,Petter Brodin,Petter Brodin +31 more
TL;DR: This article showed that a lack of bifidobacteria, and in particular depletion of genes required for human milk oligosaccharide utilization from the metagenome, is associated with systemic inflammation and immune dysregulation early in life.
Posted ContentDOI
Bifidobacteria-mediated immune system imprinting early in life
Bethany M. Henrick,Lucie Rodriguez,Tadepally Lakshmikanth,Christian Pou,Ewa Henckel,Ewa Henckel,Ewa Henckel,Axel Olin,Jun Wang,Jaromír Mikeš,Ziyang Tan,Yang Chen,Amy M. Ehrlich,Anna Karin Bernhardsson,Constantin Habimana Mugabo,Ylva Ambrosiani,Anna Gustafsson,Anna Gustafsson,Stephanie Chew,Heather Brown,Johann Prambs,Kajsa Bohlin,Kajsa Bohlin,Ryan D. Mitchell,Mark A. Underwood,Jennifer T. Smilowitz,J. Bruce German,Steven A. Frese,Petter Brodin,Petter Brodin +29 more
TL;DR: An ordered sequence of immune changes after birth, driven by microbial interactions is mapped, triggered by microbial colonization that distinguish children with different gut bacterial composition.
Journal ArticleDOI
The repertoire of maternal anti-viral antibodies in human newborns
Christian Pou,Dieudonné Nkulikiyimfura,Ewa Henckel,Ewa Henckel,Axel Olin,Tadepally Lakshmikanth,Jaromír Mikeš,Jun Wang,Yang Chen,Anna Karin Bernhardsson,Anna Karin Bernhardsson,Anna Gustafsson,Anna Gustafsson,Kajsa Bohlin,Kajsa Bohlin,Petter Brodin,Petter Brodin +16 more
TL;DR: It is found that extremely preterm children receive comparable repertoires of IgG as term children, albeit at lower absolute concentrations and consequent shorter half-life, and neutralization of the clinically important respiratory syncytial virus was also comparable until three months of age.