Early cellular innate immune responses drive Zika viral persistence and tissue tropism in pigtail macaques

The immune response to Zika virus is required to curtail the infection and avoid immunopathology, but may be involved in the associated pathophysiology. Here the authors show that viral persistence and tissue tropism is shaped by an early innate immune response in a pigtail macaque model of infectio...

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Autores principales: Megan A. O’Connor, Jennifer Tisoncik-Go, Thomas B. Lewis, Charlene J. Miller, Debra Bratt, Cassie R. Moats, Paul T. Edlefsen, Jeremy Smedley, Nichole R. Klatt, Michael Gale, Deborah Heydenburg Fuller
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Lenguaje:EN
Publicado: Nature Portfolio 2018
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Acceso en línea:https://doaj.org/article/78dc029ed4b2439e9cffb503a9b5876b
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spelling oai:doaj.org-article:78dc029ed4b2439e9cffb503a9b5876b2021-12-02T14:41:29ZEarly cellular innate immune responses drive Zika viral persistence and tissue tropism in pigtail macaques10.1038/s41467-018-05826-w2041-1723https://doaj.org/article/78dc029ed4b2439e9cffb503a9b5876b2018-08-01T00:00:00Zhttps://doi.org/10.1038/s41467-018-05826-whttps://doaj.org/toc/2041-1723The immune response to Zika virus is required to curtail the infection and avoid immunopathology, but may be involved in the associated pathophysiology. Here the authors show that viral persistence and tissue tropism is shaped by an early innate immune response in a pigtail macaque model of infection.Megan A. O’ConnorJennifer Tisoncik-GoThomas B. LewisCharlene J. MillerDebra BrattCassie R. MoatsPaul T. EdlefsenJeremy SmedleyNichole R. KlattMichael GaleDeborah Heydenburg FullerNature PortfolioarticleScienceQENNature Communications, Vol 9, Iss 1, Pp 1-11 (2018)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Megan A. O’Connor
Jennifer Tisoncik-Go
Thomas B. Lewis
Charlene J. Miller
Debra Bratt
Cassie R. Moats
Paul T. Edlefsen
Jeremy Smedley
Nichole R. Klatt
Michael Gale
Deborah Heydenburg Fuller
Early cellular innate immune responses drive Zika viral persistence and tissue tropism in pigtail macaques
description The immune response to Zika virus is required to curtail the infection and avoid immunopathology, but may be involved in the associated pathophysiology. Here the authors show that viral persistence and tissue tropism is shaped by an early innate immune response in a pigtail macaque model of infection.
format article
author Megan A. O’Connor
Jennifer Tisoncik-Go
Thomas B. Lewis
Charlene J. Miller
Debra Bratt
Cassie R. Moats
Paul T. Edlefsen
Jeremy Smedley
Nichole R. Klatt
Michael Gale
Deborah Heydenburg Fuller
author_facet Megan A. O’Connor
Jennifer Tisoncik-Go
Thomas B. Lewis
Charlene J. Miller
Debra Bratt
Cassie R. Moats
Paul T. Edlefsen
Jeremy Smedley
Nichole R. Klatt
Michael Gale
Deborah Heydenburg Fuller
author_sort Megan A. O’Connor
title Early cellular innate immune responses drive Zika viral persistence and tissue tropism in pigtail macaques
title_short Early cellular innate immune responses drive Zika viral persistence and tissue tropism in pigtail macaques
title_full Early cellular innate immune responses drive Zika viral persistence and tissue tropism in pigtail macaques
title_fullStr Early cellular innate immune responses drive Zika viral persistence and tissue tropism in pigtail macaques
title_full_unstemmed Early cellular innate immune responses drive Zika viral persistence and tissue tropism in pigtail macaques
title_sort early cellular innate immune responses drive zika viral persistence and tissue tropism in pigtail macaques
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/78dc029ed4b2439e9cffb503a9b5876b
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