Influenza a virus induces an immediate cytotoxic activity in all major subsets of peripheral blood mononuclear cells.

BACKGROUND: A replication defective influenza A vaccine virus (delNS1 virus) was developed. Its attenuation is due to potent stimulation of the innate immune system by the virus. Since the innate immune system can also target cancer cells, we reasoned that delNS1 virus induced immune-stimulation sho...

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Main Authors: Sanda Sturlan, Monika Sachet, Suzann Baumann, Irina Kuznetsova, Andreas Spittler, Michael Bergmann
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2610492?pdf=render
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author Sanda Sturlan
Monika Sachet
Suzann Baumann
Irina Kuznetsova
Andreas Spittler
Michael Bergmann
author_facet Sanda Sturlan
Monika Sachet
Suzann Baumann
Irina Kuznetsova
Andreas Spittler
Michael Bergmann
author_sort Sanda Sturlan
collection DOAJ
description BACKGROUND: A replication defective influenza A vaccine virus (delNS1 virus) was developed. Its attenuation is due to potent stimulation of the innate immune system by the virus. Since the innate immune system can also target cancer cells, we reasoned that delNS1 virus induced immune-stimulation should also lead to the induction of innate cytotoxic effects towards cancer cells. METHODOLOGY/PRINCIPAL FINDINGS: Peripheral blood mononuclear cells (PBMCs), isolated CD56+, CD3+, CD14+ and CD19+ subsets and different combinations of the above subsets were stimulated by delNS1, wild type (wt) virus or heat inactivated virus and co-cultured with tumor cell lines in the presence or absence of antibodies against the interferon system. Stimulation of PBMCs by the delNS1 virus effectively induced cytotoxicity against different cancer cell lines. Surprisingly, virus induced cytotoxicity was exerted by all major subtypes of PBMCs including CD56+, CD3+, CD14+ and CD19+ cells. Virus induced cytotoxicity in CD3+, CD14+ and CD19+ cells was dependent on virus replication, whereas virus induced cytotoxicity in CD56+ cells was only dependent on the binding of the virus. Virus induced cytotoxicity of isolated cell cultures of CD14+, CD19+ or CD56+ cells could be partially blocked by antibodies against type I and type II (IFN) interferon. In contrast, virus induced cytotoxicity in the complete PBMC preparation could not be inhibited by blocking type I or type II IFN, indicating a redundant system of activation in whole blood. CONCLUSIONS/SIGNIFICANCE: Our data suggest that apart from their well known specialized functions all main subsets of peripheral blood cells also initially exert a cytotoxic effect upon virus stimulation. This closely links the innate immune system to the adaptive immune response and renders delNS1 virus a potential therapeutic tool for viro-immunotherapy of cancer.
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spelling doaj.art-8f26db3e5ca74cfb83e850c0a24901692022-12-22T03:44:30ZengPublic Library of Science (PLoS)PLoS ONE1932-62032009-01-0141e412210.1371/journal.pone.0004122Influenza a virus induces an immediate cytotoxic activity in all major subsets of peripheral blood mononuclear cells.Sanda SturlanMonika SachetSuzann BaumannIrina KuznetsovaAndreas SpittlerMichael BergmannBACKGROUND: A replication defective influenza A vaccine virus (delNS1 virus) was developed. Its attenuation is due to potent stimulation of the innate immune system by the virus. Since the innate immune system can also target cancer cells, we reasoned that delNS1 virus induced immune-stimulation should also lead to the induction of innate cytotoxic effects towards cancer cells. METHODOLOGY/PRINCIPAL FINDINGS: Peripheral blood mononuclear cells (PBMCs), isolated CD56+, CD3+, CD14+ and CD19+ subsets and different combinations of the above subsets were stimulated by delNS1, wild type (wt) virus or heat inactivated virus and co-cultured with tumor cell lines in the presence or absence of antibodies against the interferon system. Stimulation of PBMCs by the delNS1 virus effectively induced cytotoxicity against different cancer cell lines. Surprisingly, virus induced cytotoxicity was exerted by all major subtypes of PBMCs including CD56+, CD3+, CD14+ and CD19+ cells. Virus induced cytotoxicity in CD3+, CD14+ and CD19+ cells was dependent on virus replication, whereas virus induced cytotoxicity in CD56+ cells was only dependent on the binding of the virus. Virus induced cytotoxicity of isolated cell cultures of CD14+, CD19+ or CD56+ cells could be partially blocked by antibodies against type I and type II (IFN) interferon. In contrast, virus induced cytotoxicity in the complete PBMC preparation could not be inhibited by blocking type I or type II IFN, indicating a redundant system of activation in whole blood. CONCLUSIONS/SIGNIFICANCE: Our data suggest that apart from their well known specialized functions all main subsets of peripheral blood cells also initially exert a cytotoxic effect upon virus stimulation. This closely links the innate immune system to the adaptive immune response and renders delNS1 virus a potential therapeutic tool for viro-immunotherapy of cancer.http://europepmc.org/articles/PMC2610492?pdf=render
spellingShingle Sanda Sturlan
Monika Sachet
Suzann Baumann
Irina Kuznetsova
Andreas Spittler
Michael Bergmann
Influenza a virus induces an immediate cytotoxic activity in all major subsets of peripheral blood mononuclear cells.
PLoS ONE
title Influenza a virus induces an immediate cytotoxic activity in all major subsets of peripheral blood mononuclear cells.
title_full Influenza a virus induces an immediate cytotoxic activity in all major subsets of peripheral blood mononuclear cells.
title_fullStr Influenza a virus induces an immediate cytotoxic activity in all major subsets of peripheral blood mononuclear cells.
title_full_unstemmed Influenza a virus induces an immediate cytotoxic activity in all major subsets of peripheral blood mononuclear cells.
title_short Influenza a virus induces an immediate cytotoxic activity in all major subsets of peripheral blood mononuclear cells.
title_sort influenza a virus induces an immediate cytotoxic activity in all major subsets of peripheral blood mononuclear cells
url http://europepmc.org/articles/PMC2610492?pdf=render
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