Evidence map›Paper›PMID 33827894›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2021

Prefusion F-Based Polyanhydride Nanovaccine Induces Both Humoral and Cell-Mediated Immunity Resulting in Long-Lasting Protection against Respiratory Syncytial Virus.

Laura M Stephens, Kathleen A Ross, Kody A Waldstein, Kevin L Legge, Jason S McLellan, Balaji Narasimhan, Steven M Varga

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
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

7 authors at 3 institutions in 2 countries.

Laura M StephensInterdisciplinary Graduate Program in Immunology, University of Iowa, Iowa City, IA.
Kathleen A RossDepartment of Chemical and Biological Engineering, Iowa State University, Ames, IA.
Kody A WaldsteinInterdisciplinary Graduate Program in Immunology, University of Iowa, Iowa City, IA.
Kevin L LeggeInterdisciplinary Graduate Program in Immunology, University of Iowa, Iowa City, IA.ORCID 0000-0001-9800-6854
Jason S McLellanDepartment of Molecular Biosciences, The University of Texas at Austin, Austin, TX.
Balaji NarasimhanDepartment of Chemical and Biological Engineering, Iowa State University, Ames, IA.ORCID 0000-0002-7955-5353
Steven M VargaInterdisciplinary Graduate Program in Immunology, University of Iowa, Iowa City, IA; varga@uiowa.edu.ORCID 0000-0001-7332-4290
University of Iowa · USIowa State University · USThe University of Texas at Austin · US

Funding

TRAINING PROGRAM IN FREE RADICAL AND RADIATION BIOLOGYT32CA078586 · NCI · UNIVERSITY OF IOWA · PI SPITZ, DOUGLAS ROBERT · 1999 to 2024
$5.7M
PREDOCTORAL TRAINING PROGRAM IN IMMUNOLOGYT32AI007485 · NIAID · UNIVERSITY OF IOWA · PI Kevin L Legge · 1995 to 2026
$5.4M
Balancing protection versus immunopathology by RSV-specific memory CD8 T cellsR01AI124093 · NIAID · UNIVERSITY OF IOWA · PI VARGA, STEVEN M · 2017 to 2020
$1.6M
NCI NIH HHS T32 CA078586NIAID NIH HHS R01 AI124093NIAID NIH HHS T32 AI007485
6 · The paper itself

Abstract

Respiratory syncytial virus (RSV) is a leading cause of lower respiratory tract infection in both young children and in older adults. Despite the morbidity, mortality, and high economic burden caused by RSV worldwide, no licensed vaccine is currently available. We have developed a novel RSV vaccine composed of a prefusion-stabilized variant of the fusion (F) protein (DS-Cav1) and a CpG oligodeoxynucleotide adjuvant encapsulated within polyanhydride nanoparticles, termed RSVNanoVax. A prime-boost intranasal administration of RSVNanoVax in BALB/c mice significantly alleviated weight loss and pulmonary dysfunction in response to an RSV challenge, with protection maintained up to at least 6 mo postvaccination. In addition, vaccinated mice exhibited rapid viral clearance in the lungs as early as 2 d after RSV infection in both inbred and outbred populations. Vaccination induced tissue-resident memory CD4 and CD8 T cells in the lungs, as well as RSV F-directed neutralizing Abs. Based on the robust immune response elicited and the high level of durable protection observed, our prefusion RSV F nanovaccine is a promising new RSV vaccine candidate.

Indexed as

AnimalsFemaleImmunity, CellularMiceMice, Inbred BALB CPolyanhydridesRespiratory Syncytial Virus, HumanRespiratory Syncytial Virus VaccinesPolyanhydridesRespiratory Syncytial Virus Vaccines

Identifiers

PMID33827894
PMCPMC8062305
OpenAlexW3143317552

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.