Evidence map›Paper›PMID 25415360›Full record

ArticlePloS one2014

Respiratory syncytial virus human experimental infection model: provenance, production, and sequence of low-passaged memphis-37 challenge virus.

Young-In Kim, John P DeVincenzo, Bart G Jones, Rajeev Rudraraju, Lisa Harrison, Rachel Meyers, Jeff Cehelsky, Rene Alvarez, Julia L Hurwitz

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

28 citing papers in PubMed, 55 citations in OpenAlex.

  1. Trial
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  6. Article
  7. Article
  8. Lamb Model of RSV Infection.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. From setbacks to success: lessons from the journey of RSV vaccine development.Therapeutic advances in vaccines and immunotherapy · 2024
    Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. A COVID-19 human viral challenge model. Learning from experience.Influenza and other respiratory viruses · 2020
    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

9 authors at 4 institutions in 1 country.

Young-In KimDepartment of Pediatrics, University of Tennessee Health Science Center, Memphis, Tennessee, United States of America; Children's Foundation Research Institute of Le Bonheur Children's Hospital, Memphis, Tennessee, United States of America.
John P DeVincenzoDepartment of Pediatrics, University of Tennessee Health Science Center, Memphis, Tennessee, United States of America; Department of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science Center, Memphis, Tennessee, United States of America; Children's Foundation Research Institute of Le Bonheur Children's Hospital, Memphis, Tennessee, United States of America.
Bart G JonesDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
Rajeev RudrarajuDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
Lisa HarrisonChildren's Foundation Research Institute of Le Bonheur Children's Hospital, Memphis, Tennessee, United States of America.
Rachel MeyersAlnylam Pharmaceuticals, Cambridge, Massachusetts, United States of America.
Jeff CehelskyAlnylam Pharmaceuticals, Cambridge, Massachusetts, United States of America.
Rene AlvarezAlnylam Pharmaceuticals, Cambridge, Massachusetts, United States of America.
Julia L HurwitzDepartment of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science Center, Memphis, Tennessee, United States of America; Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
Alnylam Pharmaceuticals (United States) · USUniversity of Tennessee Health Science Center · USSt. Jude Children's Research Hospital · USLe Bonheur Children's Hospital · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
Influence of maternal antibodies on a Sendai virus-vectored RSV vaccineR01AI088729 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI DEVINCENZO, JOHN P., HURWITZ, JULIA L · 2010 to 2014
$3.0M
IMMUNOGENETICS AND THE PATHOGENESIS OF RSV INFECTIONK23RR016187 · NCRR · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI DEVINCENZO, JOHN P · 2000 to 2004
$580k
NCI NIH HHS P01 P30 CA21765NCI NIH HHS P30 CA021765NCRR NIH HHS K23 RR016187NCRR NIH HHS RR 16187-01NIAID NIH HHS R01 AI088729
6 · The paper itself

Abstract

Respiratory syncytial virus (RSV) is the leading cause of lower respiratory tract infections in children and is responsible for as many as 199,000 childhood deaths annually worldwide. To support the development of viral therapeutics and vaccines for RSV, a human adult experimental infection model has been established. In this report, we describe the provenance and sequence of RSV Memphis-37, the low-passage clinical isolate used for the model's reproducible, safe, experimental infections of healthy, adult volunteers. The predicted amino acid sequences for major proteins of Memphis-37 are compared to nine other RSV A and B amino acid sequences to examine sites of vaccine, therapeutic, and pathophysiologic interest. Human T- cell epitope sequences previously defined by in vitro studies were observed to be closely matched between Memphis-37 and the laboratory strain RSV A2. Memphis-37 sequences provide baseline data with which to assess: (i) virus heterogeneity that may be evident following virus infection/transmission, (ii) the efficacy of candidate RSV vaccines and therapeutics in the experimental infection model, and (iii) the potential emergence of escape mutants as a consequence of experimental drug treatments. Memphis-37 is a valuable tool for pre-clinical research, and to expedite the clinical development of vaccines, therapeutic immunomodulatory agents, and other antiviral drug strategies for the protection of vulnerable populations against RSV disease.

Indexed as

Amino Acid SequenceAnimalsAntiviral AgentsBronchiolitisCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesChild, PreschoolChlorocebus aethiopsEpitopes, T-LymphocyteHep G2 CellsHost-Pathogen InteractionsHumansMaleMolecular Sequence DataRespiratory Syncytial Virus, HumanRespiratory Syncytial Virus InfectionsAntiviral AgentsEpitopes, T-LymphocyteRespiratory Syncytial Virus VaccinesViral Proteins

Identifiers

PMID25415360
PMCPMC4240712
OpenAlexW1965200033

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.