Evidence map›Paper›PMID 18641350›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2008

CD8+ T lymphocytes control murine cytomegalovirus replication in the central nervous system of newborn animals.

Glenn R B Bantug, Djurdijca Cekinovic, Russell Bradford, Thad Koontz, Stipan Jonjic, William J Britt

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

54 citing papers in PubMed, 74 citations in OpenAlex.

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  11. Immune surveillance of cytomegalovirus in tissues.Cellular & molecular immunology · 2024
    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

6 authors at 4 institutions in 3 countries.

Glenn R B BantugDepartment of Microbiology, University of Alabama at Birmingham, Alabama 35294, USA.
Djurdijca Cekinovic
Russell Bradford
Thad Koontz
Stipan Jonjic
William J Britt
Pediatrics and Genetics · USUniversity of Rijeka · HRCzech Academy of Sciences, Institute of Microbiology · CZUniversity of Alabama at Birmingham · US

Funding

Congenital CMV and CNS Infection Mechanisms of Protective ImmunityR01AI089956 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI William Jarvis Britt · 2011 to 2026
$7.7M
CNS MALDEVELOPMENT AND PERINANTAL INFECTIONR01HD044721 · NICHD · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BRITT, WILLIAM JARVIS · 2003 to 2007
$1.3M
Inflammation and Hearing Loss Following Congenital CMV InfectionR56DC015980 · NIDCD · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BRITT, WILLIAM JARVIS, HIROSE, KEIKO · 2016 to 2016
$100k
NIAID NIH HHS R01 AI089956NICHD NIH HHS HD 044721NICHD NIH HHS R01 HD044721NIDCD NIH HHS R56 DC015980
6 · The paper itself

Abstract

Human CMV infection of the neonatal CNS results in long-term neurologic sequelae. To define the pathogenesis of fetal human CMV CNS infections, we investigated mechanisms of virus clearance from the CNS of neonatal BALB/c mice infected with murine CMV (MCMV). Virus titers peaked in the CNS between postnatal days 10-14 and infectious virus was undetectable by postnatal day 21. Congruent with virus clearance was the recruitment of CD8(+) T cells into the CNS. Depletion of CD8(+) T cells resulted in death by postnatal day 15 in MCMV-infected animals and increased viral loads in the liver, spleen, and the CNS, suggesting an important role for these cells in the control of MCMV replication in the newborn brain. Examination of brain mononuclear cells revealed that CD8(+) T cell infiltrates expressed high levels of CD69, CD44, and CD49d. IE1(168)-specific CD8(+) T cells accumulated in the CNS and produced IFN-gamma and TNF-alpha but not IL-2 following peptide stimulation. Moreover, adoptive transfer of brain mononuclear cells resulted in decreased virus burden in immunodepleted MCMV-infected syngeneic mice. Depletion of the CD8(+) cell population following transfer eliminated control of virus replication. In summary, these results show that functionally mature virus-specific CD8(+) T cells are recruited to the CNS in mice infected with MCMV as neonates.

Indexed as

Virus ReplicationAgingAnimalsAnimals, NewbornBrainCD8-Positive T-LymphocytesCell MovementCells, CulturedCell SeparationCentral Nervous System DiseasesFemaleHerpesviridae InfectionsImmediate-Early ProteinsInterferon-gammaLiverMaleIE1 protein, cytomegalovirusImmediate-Early ProteinsInterferon-gamma

Identifiers

PMID18641350
PMCPMC4161464
OpenAlexW2149436570

What OpenQuestion holds

Textmetadata
LicenceTDM
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.