Evidence map›Paper›PMID 28554503›Full record

ArticleVaccine2017

Saccharomyces cerevisiae-derived virus-like particle parvovirus B19 vaccine elicits binding and neutralizing antibodies in a mouse model for sickle cell disease.

Rhiannon R Penkert, Neal S Young, Sherri L Surman, Robert E Sealy, Jason Rosch, Philip R Dormitzer, Ethan C Settembre, Sumana Chandramouli, Susan Wong, Jane S Hankins and 1 more

Abstract read
In one paragraph

Article in Vaccine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

10 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Sickle Cell Anemia and Its Phenotypes.Annual review of genomics and human genetics · 2018
    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

11 authors at 4 institutions in 1 country.

Rhiannon R PenkertDepartment of Infectious Diseases, St Jude Children's Research Hospital, Memphis, TN, United States.
Neal S YoungHematology Branch, National Heart, Lung and Blood Institute, Bethesda, MD, United States.
Sherri L SurmanDepartment of Infectious Diseases, St Jude Children's Research Hospital, Memphis, TN, United States.
Robert E SealyDepartment of Infectious Diseases, St Jude Children's Research Hospital, Memphis, TN, United States.
Jason RoschDepartment of Infectious Diseases, St Jude Children's Research Hospital, Memphis, TN, United States; Department of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science Center, Memphis, TN, United States.
Philip R DormitzerNovartis Vaccines and Diagnostics, Cambridge, MA, United States.
Ethan C SettembreNovartis Vaccines and Diagnostics, Cambridge, MA, United States.
Sumana ChandramouliGSK Vaccines, Rockville, MD, United States.
Susan WongHematology Branch, National Heart, Lung and Blood Institute, Bethesda, MD, United States.
Jane S HankinsDepartment of Hematology, St Jude Children's Research Hospital, Memphis, TN, United States.
Julia L HurwitzDepartment of Infectious Diseases, St Jude Children's Research Hospital, Memphis, TN, United States; Department of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science Center, Memphis, TN, United States. Electronic address: julia.hurwitz@stjude.org.
St. Jude Children's Research Hospital · USNational Heart Lung and Blood Institute · USNovartis (United States) · USGlaxoSmithKline (United States) · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
Pneumococcal pathogenesis in sickle cell diseaseR01AI110618 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI ROSCH, JASON W. · 2015 to 2019
$2.2M
NCI NIH HHS P30 CA021765NIAID NIH HHS R01 AI110618
6 · The paper itself

Abstract

Parvovirus B19 infections are typically mild in healthy individuals, but can be life threatening in individuals with sickle cell disease (SCD). A Saccharomyces cerevisiae-derived B19 VLP vaccine, now in pre-clinical development, is immunogenic in wild type mice when administered with the adjuvant MF59. Because SCD alters the immune response, we evaluated the efficacy of this vaccine in a mouse model for SCD. Vaccinated mice with SCD demonstrated similar binding and neutralizing antibody responses to those of heterozygous littermate controls following a prime-boost-boost regimen. Due to the lack of a mouse parvovirus B19 challenge model, we employed a natural mouse pathogen, Sendai virus, to evaluate SCD respiratory tract responses to infection. Normal mucosal and systemic antibody responses were observed in these mice. Results demonstrate that mice with SCD can respond to a VLP vaccine and to a respiratory virus challenge, encouraging rapid development of the B19 vaccine for patients with SCD.

Indexed as

Adjuvants, ImmunologicAnemia, Sickle CellAnimalsAntibodies, NeutralizingAntibodies, ViralDisease Models, AnimalErythema InfectiosumMiceParvovirus B19, HumanPolysorbatesRespirovirus InfectionsSaccharomyces cerevisiaeSqualeneVaccines, SyntheticVaccines, Virus-Like ParticleAdjuvants, ImmunologicAntibodies, NeutralizingAntibodies, ViralMF59 oil emulsionPolysorbatesSqualeneVaccines, SyntheticVaccines, Virus-Like ParticleIntramuscularMucosal antibody responseParvovirus B19 vaccineSickle cell diseaseSystemic antibodyYeast-derived

Identifiers

PMID28554503
PMCPMC5526597
OpenAlexW2618025695

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.