tetano
Editor, Senior Moderator
Hum Vaccin Immunother. 2020 Apr 16:1-9. doi: 10.1080/21645515.2020.1711677. [Epub ahead of print]
Differential gene expression in peripheral blood mononuclear cells from children immunized with inactivated influenza vaccine.
Alcorn JF[SUP]1[/SUP], Avula R[SUP]2[/SUP], Chakka AB[SUP]2[/SUP], Schwarzmann WE[SUP]2[/SUP], Nowalk MP[SUP]3[/SUP], Lin CJ[SUP]3[/SUP], Ortiz MA[SUP]1,[/SUP][SUP]4[/SUP], Horne WT[SUP]1[/SUP], Chandran UR[SUP]2[/SUP], Nagg JP[SUP]1[/SUP], Zimmerman RK[SUP]3[/SUP], Cole KS[SUP]4[/SUP], Moehling KK[SUP]3[/SUP], Martin JM[SUP]1[/SUP].
Author information
Abstract
The human immune response to inactivated influenza vaccine is dynamic and impacted by age and preexisting immunity. Our goal was to identify postvaccination transcriptomic changes in peripheral blood mononuclear cells from children. Blood samples were obtained before and at 3 or 7 days postvaccination with 2016-2017 quadrivalent inactivated influenza vaccine and RNA sequencing was performed. There were 1,466 differentially expressed genes (DEGs) for the Day 0-Day 3 group and 513 DEGs for the Day 0-Day 7 group. Thirty-three genes were common between the two groups. The majority of the transcriptomic changes at Day 3 represented innate inflammation and apoptosis pathways. Day 7 DEGs were characterized by activation of cellular processes, including the regulation of cytoskeleton, junctions, and metabolism, and increased expression of immunoglobulin genes. DEGs at Day 3 were compared between older and younger children revealing increased inflammatory gene expression in the older group. Vaccine history in the year prior to the study was characterized by robust DEGs at Day 3 with decreased phagosome and dendritic cell maturation in those who had been vaccinated in the previous year. PBMC responses to inactivated influenza vaccination in children differed significantly by the timing of sampling, patient age, and vaccine history. These data provide insight into the expected molecular pathways to be temporally altered by influenza vaccination in children.
KEYWORDS:
Influenza; RNA sequencing; immunity; inflammation; pediatrics
PMID:32298194DOI:10.1080/21645515.2020.1711677
Differential gene expression in peripheral blood mononuclear cells from children immunized with inactivated influenza vaccine.
Alcorn JF[SUP]1[/SUP], Avula R[SUP]2[/SUP], Chakka AB[SUP]2[/SUP], Schwarzmann WE[SUP]2[/SUP], Nowalk MP[SUP]3[/SUP], Lin CJ[SUP]3[/SUP], Ortiz MA[SUP]1,[/SUP][SUP]4[/SUP], Horne WT[SUP]1[/SUP], Chandran UR[SUP]2[/SUP], Nagg JP[SUP]1[/SUP], Zimmerman RK[SUP]3[/SUP], Cole KS[SUP]4[/SUP], Moehling KK[SUP]3[/SUP], Martin JM[SUP]1[/SUP].
Author information
Abstract
The human immune response to inactivated influenza vaccine is dynamic and impacted by age and preexisting immunity. Our goal was to identify postvaccination transcriptomic changes in peripheral blood mononuclear cells from children. Blood samples were obtained before and at 3 or 7 days postvaccination with 2016-2017 quadrivalent inactivated influenza vaccine and RNA sequencing was performed. There were 1,466 differentially expressed genes (DEGs) for the Day 0-Day 3 group and 513 DEGs for the Day 0-Day 7 group. Thirty-three genes were common between the two groups. The majority of the transcriptomic changes at Day 3 represented innate inflammation and apoptosis pathways. Day 7 DEGs were characterized by activation of cellular processes, including the regulation of cytoskeleton, junctions, and metabolism, and increased expression of immunoglobulin genes. DEGs at Day 3 were compared between older and younger children revealing increased inflammatory gene expression in the older group. Vaccine history in the year prior to the study was characterized by robust DEGs at Day 3 with decreased phagosome and dendritic cell maturation in those who had been vaccinated in the previous year. PBMC responses to inactivated influenza vaccination in children differed significantly by the timing of sampling, patient age, and vaccine history. These data provide insight into the expected molecular pathways to be temporally altered by influenza vaccination in children.
KEYWORDS:
Influenza; RNA sequencing; immunity; inflammation; pediatrics
PMID:32298194DOI:10.1080/21645515.2020.1711677