Evidence map›Paper›PMID 28663436›Full record

ArticleThe Journal of experimental medicine2017

Keratinocytes produce IL-17c to protect peripheral nervous systems during human HSV-2 reactivation.

Tao Peng, R Savanh Chanthaphavong, Sijie Sun, James A Trigilio, Khamsone Phasouk, Lei Jin, Erik D Layton, Alvason Z Li, Colin E Correnti, Willem De van der Schueren and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.1field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 62 citations in OpenAlex.

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  10. The IL-17 family in diseases: from bench to bedside.Signal transduction and targeted therapy · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 1 country.

Tao PengDepartment of Laboratory Medicine, University of Washington, Seattle, WA tpeng@uw.edu.ORCID http://orcid.org/0000-0001-9982-6053
R Savanh ChanthaphavongDepartment of Laboratory Medicine, University of Washington, Seattle, WA.
Sijie SunDepartment of Laboratory Medicine, University of Washington, Seattle, WA.ORCID http://orcid.org/0000-0002-6232-5121
James A TrigilioDepartment of Laboratory Medicine, University of Washington, Seattle, WA.
Khamsone PhasoukVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Lei JinVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA.ORCID http://orcid.org/0000-0002-7841-7266
Erik D LaytonVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Alvason Z LiVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA.ORCID http://orcid.org/0000-0001-6889-3288
Colin E CorrentiClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Willem De van der SchuerenClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA.
Julio VazquezShared Resources Scientific Imaging, Fred Hutchinson Cancer Research Center, Seattle, WA.ORCID http://orcid.org/0000-0001-6187-2644
Diana R O'DayLaboratory of Developmental Biology, University of Washington, Seattle, WA.
Ian A GlassLaboratory of Developmental Biology, University of Washington, Seattle, WA.ORCID http://orcid.org/0000-0001-6762-8407
David M KnipeDepartment of Microbiology and Immunobiology, Harvard Medical School, Boston, MA.
Anna WaldDepartment of Laboratory Medicine, University of Washington, Seattle, WA.ORCID http://orcid.org/0000-0003-3486-6438
Lawrence CoreyDepartment of Laboratory Medicine, University of Washington, Seattle, WA.ORCID http://orcid.org/0000-0002-2179-2436
Jia ZhuDepartment of Laboratory Medicine, University of Washington, Seattle, WA jiazhu@uw.edu.ORCID http://orcid.org/0000-0002-8676-5105
Infectious Disease Research Institute · USUniversity of Washington · USFred Hutch Cancer Center · USHarvard University · US

Funding

THE PERINATAL COMPLICATIONS OF ASYMPTOMATIC GENITAL HERPES SIMPLEX VIRUSP01AI030731 · NIAID · UNIVERSITY OF WASHINGTON · PI ZHU, JIA · 1991 to 2017
$34.3M
LABORATORY OF DEVELOPMENTAL BIOLOGYR24HD000836 · NICHD · UNIVERSITY OF WASHINGTON · PI Ian Amos Glass · 1995 to 2026
$16.9M
Genetics of Herpesvirus TransformationR01AI063106 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI KNIPE, DAVID M. · 2004 to 2013
$3.8M
CYTOTOXIC T CELL RESPONSES TO HSV IN HIV INFECTIONR01AI042528 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI COREY, LAWRENCE, ZHU, JIA · 1998 to 2016
$2.7M
Mechanisms of Protective Local Immunity in Human Female Reproductive TractR01AI111780 · NIAID · UNIVERSITY OF WASHINGTON · PI ZHU, JIA · 2014 to 2018
$1.7M
Mechanisms of CD8+ T cell Immune surveillance in human genital skin and mucosa afR56AI093746 · NIAID · UNIVERSITY OF WASHINGTON · PI ZHU, JIA · 2012 to 2012
$318k
NIAID NIH HHS P01 AI030731NIAID NIH HHS R01 AI042528NIAID NIH HHS R01 AI063106NIAID NIH HHS R01 AI111780NIAID NIH HHS R56 AI093746NICHD NIH HHS R24 HD000836
6 · The paper itself

Abstract

Despite frequent herpes simplex virus (HSV) reactivation, peripheral nerve destruction and sensory anesthesia are rare. We discovered that skin biopsies obtained during asymptomatic human HSV-2 reactivation exhibit a higher density of nerve fibers relative to biopsies during virological and clinical quiescence. We evaluated the effects of HSV infection on keratinocytes, the initial target of HSV replication, to better understand this observation. Keratinocytes produced IL-17c during HSV-2 reactivation, and IL-17RE, an IL-17c-specific receptor, was expressed on nerve fibers in human skin and sensory neurons in dorsal root ganglia. In ex vivo experiments, exogenous human IL-17c provided directional guidance and promoted neurite growth and branching in microfluidic devices. Exogenous murine IL-17c pretreatment reduced apoptosis in HSV-2-infected primary neurons. These results suggest that IL-17c is a neurotrophic cytokine that protects peripheral nerve systems during HSV reactivation. This mechanism could explain the lack of nerve damage from recurrent HSV infection and may provide insight to understanding and treating sensory peripheral neuropathies.

Indexed as

AnimalsHerpes GenitalisHerpesvirus 2, HumanHumansInterleukin-17KeratinocytesNeuritesNeuroblastomaPeripheral Nervous SystemVirus ActivationInterleukin-17

Identifiers

PMID28663436
PMCPMC5551564
OpenAlexW2732375683

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.