Evidence map›Paper›PMID 18842707›Full record

ArticleJournal of virology2008

Passive immunization reduces murine cytomegalovirus-induced brain pathology in newborn mice.

Durdica Cekinović, Mijo Golemac, Ester Pernjak Pugel, Jelena Tomac, Luka Cicin-Sain, Irena Slavuljica, Russell Bradford, Sonja Misch, Thomas H Winkler, Michael Mach and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

51 citing papers in PubMed, 84 citations in OpenAlex.

  1. A viral glycoprotein targets IgGEMBO molecular medicine · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Immune surveillance of cytomegalovirus in tissues.Cellular & molecular immunology · 2024
    Review
  6. Article
  7. Article
  8. Anti-CMV therapy, what next? A systematic review.Frontiers in microbiology · 2023
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Rodent Models of Congenital Cytomegalovirus Infection.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. Review
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

12 authors at 4 institutions in 3 countries.

Durdica CekinovićDepartment of Histology and Embryology, Faculty of Medicine, University of Rijeka, B Branchetta 20, Rijeka 51000, Croatia.
Mijo Golemac
Ester Pernjak Pugel
Jelena Tomac
Luka Cicin-Sain
Irena Slavuljica
Russell Bradford
Sonja Misch
Thomas H Winkler
Michael Mach
William J Britt
Stipan Jonjić
University of Rijeka · HRFriedrich-Alexander-Universität Erlangen-Nürnberg · DEUniversity of Alabama at Birmingham · USUniversitätsklinikum Erlangen · DE

Funding

CNS MALDEVELOPMENT AND PERINANTAL INFECTIONR01HD044721 · NICHD · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BRITT, WILLIAM JARVIS · 2003 to 2007
$1.3M
NICHD NIH HHS R01 HD044721
6 · The paper itself

Abstract

Human cytomegalovirus (HCMV) is the most frequent cause of congenital viral infections in humans and frequently leads to long-term central nervous system (CNS) abnormalities that include learning disabilities, microcephaly, and hearing loss. The pathogenesis of the CNS infection has not been fully elucidated and may arise as a result of direct damage of CMV-infected neurons or indirectly secondary to inflammatory response to infection. We used a recently established model of mouse CMV (MCMV) infection in newborn mice to analyze the contribution of humoral immunity to virus clearance from the brain. In brains of MCMV-infected newborn mice treated with immune serum, the titer of infectious virus was reduced below detection limit, whereas in the brains of mice receiving control (nonimmune) serum significant amounts of virus were recovered. Moreover, histopathological and immunohistological analyses revealed significantly less CNS inflammation in mice treated with immune serum. Treatment with MCMV-specific monoclonal antibodies also resulted in the reduction of virus titer in the brain. Recipients of control serum or irrelevant antibodies had more viral foci, marked mononuclear cell infiltrates, and prominent glial nodules in their brains than mice treated with immune serum or MCMV-specific antibodies. In conclusion, our data indicate that virus-specific antibodies have a protective role in the development of CNS pathology in MCMV-infected newborn mice, suggesting that antiviral antibodies may be an important component of protective immunological responses during CMV infection of the developing CNS.

Indexed as

Immunization, PassiveAnimalsAnimals, NewbornAntibodies, MonoclonalAntibodies, ViralBrain DiseasesImmune SeraKineticsMiceMice, Inbred BALB CMuromegalovirusVirus ReplicationAntibodies, MonoclonalAntibodies, ViralImmune Sera

Identifiers

PMID18842707
PMCPMC2593357
OpenAlexW2067092950

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.