Evidence map›Paper›PMID 32161194›Full record

ArticleJCI insight2020

T cell response kinetics determines neuroinfection outcomes during murine HSV infection.

Aisha G Lee, Jason M Scott, Maria Rita Fabbrizi, Xiaoping Jiang, Dorothy K Sojka, Mark J Miller, Megan T Baldridge, Wayne M Yokoyama, Haina Shin

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Aisha G LeeDivision of Infectious Diseases and.
Jason M ScottDivision of Infectious Diseases and.
Maria Rita FabbriziDivision of Infectious Diseases and.
Xiaoping JiangDivision of Infectious Diseases and.
Dorothy K SojkaDivision of Rheumatology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Mark J MillerDivision of Infectious Diseases and.
Megan T BaldridgeDivision of Infectious Diseases and.
Wayne M YokoyamaDivision of Rheumatology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.
Haina ShinDivision of Infectious Diseases and.
Office of Infectious Diseases · USWashington University in St. Louis · US

Funding

TRAINING PROGRAM IN IMMUNOLOGY AND IMMUNOGENETICST32AI007163 · NIAID · WASHINGTON UNIVERSITY · PI Kenneth M Murphy, Kodi S Ravichandran · 1985 to 2026
$14.8M
Epithelial Responses to Bacterial InvasionR01AI077600 · NIAID · WASHINGTON UNIVERSITY · PI MILLER, MARK JAMES · 2009 to 2021
$3.8M
THE ROLE OF NEUTROPHILS IN REGULATING DISEASE SEVERITY OF VIRAL SEXUALLY TRANSMITTED INFECTIONSR01AI134962 · NIAID · WASHINGTON UNIVERSITY · PI SHAN, LIANG · 2018 to 2022
$2.0M
A novel PCR-based method for quantification of antibody-dependent clearance of HIV-1 reservoirsR21AI150418 · NIAID · WASHINGTON UNIVERSITY · PI SHAN, LIANG · 2020 to 2021
$433k
NIAID NIH HHS R01 AI077600NIAID NIH HHS R01 AI134962NIAID NIH HHS R21 AI150418NIAID NIH HHS T32 AI007163
6 · The paper itself

Abstract

Herpes simplex virus-2 (HSV-2) and HSV-1 both can cause genital herpes, a chronic infection that establishes a latent reservoir in the nervous system. Clinically, the recurrence frequency of HSV-1 genital herpes is considerably less than HSV-2 genital herpes, which correlates with reduced neuronal infection. The factors dictating the disparate outcomes of HSV-1 and HSV-2 genital herpes are unclear. In this study, we show that vaginal infection of mice with HSV-1 leads to the rapid appearance of mature DCs in the draining lymph node, which is dependent on an early burst of NK cell-mediated IFN-γ production in the vagina that occurs after HSV-1 infection but not HSV-2 infection. Rapid DC maturation after HSV-1 infection, but not HSV-2 infection, correlates with the accelerated generation of a neuroprotective T cell response and early accumulation of IFN-γ-producing T cells at the site of infection. Depletion of T cells or loss of IFN-γ receptor (IFN-γR) expression in sensory neurons both lead to a marked loss of neuroprotection only during HSV-1, recapitulating a prominent feature of HSV-2 infection. Our experiments reveal key differences in host control of neuronal HSV-1 and HSV-2 infection after genital exposure of mice, and they define parameters of a successful immune response against genital herpes.

Indexed as

AnimalsCell DifferentiationFemaleHerpes SimplexHerpesvirus 1, HumanHerpesvirus 2, HumanHost-Pathogen InteractionsInterferon-gammaMiceMice, Inbred C57BLNervous System DiseasesT-LymphocytesInterferon-gammaAdaptive immunityImmunologyInfectious disease

Identifiers

PMID32161194
PMCPMC7141405
OpenAlexW3011558042

What OpenQuestion holds

Textmetadata
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.