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What Lies Beneath: Antibody Dependent Natural Killer Cell Activation by Antibodies to Internal Influenza Virus Proteins

The conserved internal influenza proteins nucleoprotein (NP) and matrix 1 (M1) are well characterised for T cell immunity, but whether they also elicit functional antibodies capable of activating natural killer (NK) cells has not been explored. We studied NP and M1-specific ADCC activity using bioch...

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Autores principales: Vanderven, Hillary A., Ana-Sosa-Batiz, Fernanda, Jegaskanda, Sinthujan, Rockman, Steven, Laurie, Karen, Barr, Ian, Chen, Weisan, Wines, Bruce, Hogarth, P. Mark, Lambe, Teresa, Gilbert, Sarah C., Parsons, Matthew S., Kent, Stephen J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4919476/
https://www.ncbi.nlm.nih.gov/pubmed/27428437
http://dx.doi.org/10.1016/j.ebiom.2016.04.029
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author Vanderven, Hillary A.
Ana-Sosa-Batiz, Fernanda
Jegaskanda, Sinthujan
Rockman, Steven
Laurie, Karen
Barr, Ian
Chen, Weisan
Wines, Bruce
Hogarth, P. Mark
Lambe, Teresa
Gilbert, Sarah C.
Parsons, Matthew S.
Kent, Stephen J.
author_facet Vanderven, Hillary A.
Ana-Sosa-Batiz, Fernanda
Jegaskanda, Sinthujan
Rockman, Steven
Laurie, Karen
Barr, Ian
Chen, Weisan
Wines, Bruce
Hogarth, P. Mark
Lambe, Teresa
Gilbert, Sarah C.
Parsons, Matthew S.
Kent, Stephen J.
author_sort Vanderven, Hillary A.
collection PubMed
description The conserved internal influenza proteins nucleoprotein (NP) and matrix 1 (M1) are well characterised for T cell immunity, but whether they also elicit functional antibodies capable of activating natural killer (NK) cells has not been explored. We studied NP and M1-specific ADCC activity using biochemical, NK cell activation and killing assays with plasma from healthy and influenza-infected subjects. Healthy adults had antibodies to M1 and NP capable of binding dimeric FcγRIIIa and activating NK cells. Natural symptomatic and experimental influenza infections resulted in a rise in antibody dependent NK cell activation post-infection to the hemagglutinin of the infecting strain, but changes in NK cell activation to M1 and NP were variable. Although antibody dependent killing of target cells infected with vaccinia viruses expressing internal influenza proteins was not detected, opsonising antibodies to NP and M1 likely contribute to an antiviral microenvironment by stimulating innate immune cells to secrete cytokines early in infection. We conclude that effector cell activating antibodies to conserved internal influenza proteins are common in healthy and influenza-infected adults. Given the significance of such antibodies in animal models of heterologous influenza infection, the definition of their importance and mechanism of action in human immunity to influenza is essential.
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spelling pubmed-49194762016-06-30 What Lies Beneath: Antibody Dependent Natural Killer Cell Activation by Antibodies to Internal Influenza Virus Proteins Vanderven, Hillary A. Ana-Sosa-Batiz, Fernanda Jegaskanda, Sinthujan Rockman, Steven Laurie, Karen Barr, Ian Chen, Weisan Wines, Bruce Hogarth, P. Mark Lambe, Teresa Gilbert, Sarah C. Parsons, Matthew S. Kent, Stephen J. EBioMedicine Research Paper The conserved internal influenza proteins nucleoprotein (NP) and matrix 1 (M1) are well characterised for T cell immunity, but whether they also elicit functional antibodies capable of activating natural killer (NK) cells has not been explored. We studied NP and M1-specific ADCC activity using biochemical, NK cell activation and killing assays with plasma from healthy and influenza-infected subjects. Healthy adults had antibodies to M1 and NP capable of binding dimeric FcγRIIIa and activating NK cells. Natural symptomatic and experimental influenza infections resulted in a rise in antibody dependent NK cell activation post-infection to the hemagglutinin of the infecting strain, but changes in NK cell activation to M1 and NP were variable. Although antibody dependent killing of target cells infected with vaccinia viruses expressing internal influenza proteins was not detected, opsonising antibodies to NP and M1 likely contribute to an antiviral microenvironment by stimulating innate immune cells to secrete cytokines early in infection. We conclude that effector cell activating antibodies to conserved internal influenza proteins are common in healthy and influenza-infected adults. Given the significance of such antibodies in animal models of heterologous influenza infection, the definition of their importance and mechanism of action in human immunity to influenza is essential. Elsevier 2016-04-28 /pmc/articles/PMC4919476/ /pubmed/27428437 http://dx.doi.org/10.1016/j.ebiom.2016.04.029 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Vanderven, Hillary A.
Ana-Sosa-Batiz, Fernanda
Jegaskanda, Sinthujan
Rockman, Steven
Laurie, Karen
Barr, Ian
Chen, Weisan
Wines, Bruce
Hogarth, P. Mark
Lambe, Teresa
Gilbert, Sarah C.
Parsons, Matthew S.
Kent, Stephen J.
What Lies Beneath: Antibody Dependent Natural Killer Cell Activation by Antibodies to Internal Influenza Virus Proteins
title What Lies Beneath: Antibody Dependent Natural Killer Cell Activation by Antibodies to Internal Influenza Virus Proteins
title_full What Lies Beneath: Antibody Dependent Natural Killer Cell Activation by Antibodies to Internal Influenza Virus Proteins
title_fullStr What Lies Beneath: Antibody Dependent Natural Killer Cell Activation by Antibodies to Internal Influenza Virus Proteins
title_full_unstemmed What Lies Beneath: Antibody Dependent Natural Killer Cell Activation by Antibodies to Internal Influenza Virus Proteins
title_short What Lies Beneath: Antibody Dependent Natural Killer Cell Activation by Antibodies to Internal Influenza Virus Proteins
title_sort what lies beneath: antibody dependent natural killer cell activation by antibodies to internal influenza virus proteins
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4919476/
https://www.ncbi.nlm.nih.gov/pubmed/27428437
http://dx.doi.org/10.1016/j.ebiom.2016.04.029
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