Evidence map›Paper›PMID 14972563›Full record

ArticleVirology2004

Differential regulation of innate and adaptive immune responses in viral encephalitis.

Julia D Rempel, Shannon J Murray, Jeffrey Meisner, Michael J Buchmeier

Open access · greenAbstract read
In one paragraph

Article in Virology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

58 citing papers in PubMed, 94 citations in OpenAlex.

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  19. Pathogenesis of murine coronavirus in the central nervous system.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2010
    Review
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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

4 authors at 1 institution in 2 countries.

Julia D RempelDivision of Virology, Department of Neuropharmacology, The Scripps Research Institute, La Jolla, CA 92037, USA.
Shannon J Murray
Jeffrey Meisner
Michael J Buchmeier
Scripps Research Institute · US

Funding

Therapeutics Core (Page 286)P30MH062261 · NIMH · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BUCH, SHILPA J., FOX, HOWARD S · 2000 to 2021
$37.7M
MECHANISMS OF MURINE CORONAVIRUS NEUROVIRULENCER01AI025913 · NIAID · SCRIPPS RESEARCH INSTITUTE · PI BUCHMEIER, MICHAEL · 1988 to 2003
$1.3M
CONTROL OF MHV INFECTION IN THE CENTRAL NERVOUS SYSTEMR01AI043103 · NIAID · SCRIPPS RESEARCH INSTITUTE · PI BUCHMEIER, MICHAEL · 1998 to 2002
$862k
NIAID NIH HHS AI-25913NIAID NIH HHS AI-43103NIAID NIH HHS R01 AI025913NIMH NIH HHS MH-62261NIMH NIH HHS P30 MH062261NIMH NIH HHS P30MH62261
6 · The paper itself

Abstract

Viral encephalitis is a global health concern. The ability of a virus to modulate the immune response can have a pivotal effect on the course of disease and the fate of the infected host. In this study, we sought to understand the immunological basis for the fatal encephalitis following infection with the murine coronavirus, mouse hepatitis virus (MHV)-JHM, in contrast with the more attenuated MHV-A59. Distinct glial cell cytokine and chemokine response patterns were observed within 3 days after infection, became progressively more polarized during the course of infection and with the infiltration of leukocytes. In the brain, MHV-JHM infection induced strong accumulation of IFNbeta mRNA relative to IFNgamma mRNA. This trend was reversed in MHV-A59 infection and was accompanied by increased CD8 T cell infiltration into brain compared to MHV-JHM infection. Increased apoptosis appeared to contribute to the diminished presence of CD8 T cells in MHV-JHM-infected brain with the consequence of a lower potential for IFNgamma production and antiviral activity. MHV-JHM infection also induced sustained mRNA accumulation of the innate immune response products interleukin (IL)-6 and IL-1. Furthermore, high levels of macrophage-inflammatory protein (MIP)-1alpha, MIP-1beta, and MIP-2 mRNA were observed at the onset of MHV-JHM infection and correlated with a marked elevation in the number of macrophages in the brain on day 7 compared to MHV-A59 infection. These observations indicate that differences in the severity of viral encephalitis may reflect the differential ability of viruses to stimulate innate immune responses within the CNS and subsequently the character of infiltrating leukocyte populations.

Indexed as

Gene Expression RegulationImmunity, InnateAnimalsBrainCD8-Positive T-LymphocytesCoronavirus InfectionsCytokinesEncephalitis, ViralMacrophagesMaleMiceMice, Inbred C57BLMurine hepatitis virusSeverity of Illness IndexCytokines

Identifiers

PMID14972563
PMCPMC7126141
OpenAlexW2008488944

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.