Human Zika infection induces a reduction of IFN-γ producing CD4 T-cells and a parallel expansion of effector Vδ2 T-cells

Abstract The definition of the immunological response to Zika (ZIKV) infection in humans represents a key issue to identify protective profile useful for vaccine development and for pathogenesis studies. No data are available on the cellular immune response in the acute phase of human ZIKV infection...

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Autores principales: Eleonora Cimini, Concetta Castilletti, Alessandra Sacchi, Rita Casetti, Veronica Bordoni, Antonella Romanelli, Federica Turchi, Federico Martini, Nicola Tumino, Emanuele Nicastri, Angela Corpolongo, Antonino Di Caro, Gary Kobinger, Alimuddin Zumla, Maria Rosaria Capobianchi, Giuseppe Ippolito, Chiara Agrati
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Publicado: Nature Portfolio 2017
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spelling oai:doaj.org-article:e211ed0897014f748616b1a30cb3342e2021-12-02T16:07:59ZHuman Zika infection induces a reduction of IFN-γ producing CD4 T-cells and a parallel expansion of effector Vδ2 T-cells10.1038/s41598-017-06536-x2045-2322https://doaj.org/article/e211ed0897014f748616b1a30cb3342e2017-07-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-06536-xhttps://doaj.org/toc/2045-2322Abstract The definition of the immunological response to Zika (ZIKV) infection in humans represents a key issue to identify protective profile useful for vaccine development and for pathogenesis studies. No data are available on the cellular immune response in the acute phase of human ZIKV infection, and its role in the protection and/or pathogenesis needs to be clarified. We studied and compared the phenotype and functionality of T-cells in patients with acute ZIKV and Dengue viral (DENV) infections. A significant activation of T-cells was observed during both ZIKV and DENV infections. ZIKV infection was characterized by a CD4 T cell differentiation toward effector cells and by a lower frequency of IFN-γ producing CD4 T cells. Moreover, a substantial expansion of CD3+CD4−CD8− T-cell subset expressing Vδ2 TCR was specifically observed in ZIKV patients. Vδ2 T cells presented a terminally differentiated profile, expressed granzyme B and maintained their ability to produce IFN-γ. These findings provide new knowledge on the immune response profile during self-limited infection that may help in vaccine efficacy definition, and in identifying possible immuno-pathogenetic mechanisms of severe infection.Eleonora CiminiConcetta CastillettiAlessandra SacchiRita CasettiVeronica BordoniAntonella RomanelliFederica TurchiFederico MartiniNicola TuminoEmanuele NicastriAngela CorpolongoAntonino Di CaroGary KobingerAlimuddin ZumlaMaria Rosaria CapobianchiGiuseppe IppolitoChiara AgratiNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-10 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Eleonora Cimini
Concetta Castilletti
Alessandra Sacchi
Rita Casetti
Veronica Bordoni
Antonella Romanelli
Federica Turchi
Federico Martini
Nicola Tumino
Emanuele Nicastri
Angela Corpolongo
Antonino Di Caro
Gary Kobinger
Alimuddin Zumla
Maria Rosaria Capobianchi
Giuseppe Ippolito
Chiara Agrati
Human Zika infection induces a reduction of IFN-γ producing CD4 T-cells and a parallel expansion of effector Vδ2 T-cells
description Abstract The definition of the immunological response to Zika (ZIKV) infection in humans represents a key issue to identify protective profile useful for vaccine development and for pathogenesis studies. No data are available on the cellular immune response in the acute phase of human ZIKV infection, and its role in the protection and/or pathogenesis needs to be clarified. We studied and compared the phenotype and functionality of T-cells in patients with acute ZIKV and Dengue viral (DENV) infections. A significant activation of T-cells was observed during both ZIKV and DENV infections. ZIKV infection was characterized by a CD4 T cell differentiation toward effector cells and by a lower frequency of IFN-γ producing CD4 T cells. Moreover, a substantial expansion of CD3+CD4−CD8− T-cell subset expressing Vδ2 TCR was specifically observed in ZIKV patients. Vδ2 T cells presented a terminally differentiated profile, expressed granzyme B and maintained their ability to produce IFN-γ. These findings provide new knowledge on the immune response profile during self-limited infection that may help in vaccine efficacy definition, and in identifying possible immuno-pathogenetic mechanisms of severe infection.
format article
author Eleonora Cimini
Concetta Castilletti
Alessandra Sacchi
Rita Casetti
Veronica Bordoni
Antonella Romanelli
Federica Turchi
Federico Martini
Nicola Tumino
Emanuele Nicastri
Angela Corpolongo
Antonino Di Caro
Gary Kobinger
Alimuddin Zumla
Maria Rosaria Capobianchi
Giuseppe Ippolito
Chiara Agrati
author_facet Eleonora Cimini
Concetta Castilletti
Alessandra Sacchi
Rita Casetti
Veronica Bordoni
Antonella Romanelli
Federica Turchi
Federico Martini
Nicola Tumino
Emanuele Nicastri
Angela Corpolongo
Antonino Di Caro
Gary Kobinger
Alimuddin Zumla
Maria Rosaria Capobianchi
Giuseppe Ippolito
Chiara Agrati
author_sort Eleonora Cimini
title Human Zika infection induces a reduction of IFN-γ producing CD4 T-cells and a parallel expansion of effector Vδ2 T-cells
title_short Human Zika infection induces a reduction of IFN-γ producing CD4 T-cells and a parallel expansion of effector Vδ2 T-cells
title_full Human Zika infection induces a reduction of IFN-γ producing CD4 T-cells and a parallel expansion of effector Vδ2 T-cells
title_fullStr Human Zika infection induces a reduction of IFN-γ producing CD4 T-cells and a parallel expansion of effector Vδ2 T-cells
title_full_unstemmed Human Zika infection induces a reduction of IFN-γ producing CD4 T-cells and a parallel expansion of effector Vδ2 T-cells
title_sort human zika infection induces a reduction of ifn-γ producing cd4 t-cells and a parallel expansion of effector vδ2 t-cells
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/e211ed0897014f748616b1a30cb3342e
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