Evidence map›Paper›PMID 28403874›Full record

ArticleVirology journal2017

Intranasal immunization of pigs with porcine reproductive and respiratory syndrome virus-like particles plus 2', 3'-cGAMP VacciGrade™ adjuvant exacerbates viremia after virus challenge.

Alexandria Van Noort, April Nelsen, Angela E Pillatzki, Diego G Diel, Feng Li, Eric Nelson, Xiuqing Wang

Open access · goldAbstract read
In one paragraph

Article in Virology journal, 2017. 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
1.1field-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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. cGAMP the travelling messenger.Frontiers in immunology · 2023
    Review
  6. Article
  7. Review
  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 1 institution in 1 country.

Alexandria Van NoortDepartment of Biology and Microbiology, South Dakota State University, Brookings, SD, 57007, USA.
April NelsenDepartment of Biology and Microbiology, South Dakota State University, Brookings, SD, 57007, USA.
Angela E PillatzkiDepartment of Veterinary and Biomedical Sciences, South Dakota State University, Brookings, SD, 57007, USA.
Diego G DielDepartment of Veterinary and Biomedical Sciences, South Dakota State University, Brookings, SD, 57007, USA.
Feng LiDepartment of Biology and Microbiology, South Dakota State University, Brookings, SD, 57007, USA.
Eric NelsonDepartment of Veterinary and Biomedical Sciences, South Dakota State University, Brookings, SD, 57007, USA.
Xiuqing WangDepartment of Biology and Microbiology, South Dakota State University, Brookings, SD, 57007, USA. Xiuqing.wang@sdstate.edu.ORCID 0000-0003-0491-4937
South Dakota State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPorcine reproductive and respiratory syndrome virus (PRRSV) causes reproductive failure in pregnant sows and acute respiratory disease in young pigs. It is a leading infectious agent of swine respiratory complex, which has significant negative economic impact on the swine industry. Commercial markets currently offer both live attenuated and killed vaccines; however, increasing controversy exists about their efficacy providing complete protection. Virus-like particles (VLPs) possess many desirable features of a potent vaccine candidate and have been proven to be highly immunogenic and protective against virus infections. Here we explored the efficacy of PRRSV VLPs together with the use of a novel 2', 3'-cGAMP VacciGrade™ adjuvant.

methodsAnimals were immunized twice intranasally with phosphate buffered saline (PBS), PRRSV VLPs, or PRRSV VLPs plus 2', 3'-cGAMP VacciGrade™ at 2 weeks apart. Animals were challenged with PRRSV-23983 at 2 weeks post the second immunization. PRRSV specific antibody response and cytokines were measured. Viremia, clinical signs, and histological lesions were evaluated.

resultsPRRSV N protein specific antibody was detected in all animals at day 10 after challenge, but no significant difference was observed among the vaccinated and control groups. Surprisingly, a significantly higher viremia was observed in the VLPs and VLPs plus the adjuvant groups compared to the control group. The increased viremia is correlated with a higher interferon-α induction in the serum of the VLPs and the VLPs plus the adjuvant groups.

conclusionsIntranasal immunizations of pigs with PRRSV VLPs and VLPs plus the 2', 3'-cGAMP VacciGrade™ adjuvant exacerbates viremia. A higher level of interferon-α production, but not interferon-γ and IL-10, is correlated with enhanced virus replication. Overall, PRRSV VLPs and PRRSV VLPs plus the adjuvant fail to provide protection against PRRSV challenge. Different dose of VLPs and alternative route of vaccination such as intramuscular injection should be explored in the future studies to fully assess the feasibility of such a vaccine platform for PRRSV control and prevention.

Indexed as

Adjuvants, ImmunologicAdministration, IntranasalAnimalsAntibodies, ViralAntibody FormationCytokinesImmunizationPorcine Reproductive and Respiratory SyndromePorcine respiratory and reproductive syndrome virusRandom AllocationSwineVaccines, Virus-Like ParticleViral VaccinesViremiaVirus ReplicationAdjuvants, ImmunologicAntibodies, ViralCytokinesVaccines, Virus-Like ParticleViral Vaccines2′, 3′-cGAMP vaccigrade™Increased viremiaInterferon-αIntranasal immunizationPRRSVVirus-like particles

Identifiers

PMID28403874
PMCPMC5389191
OpenAlexW2606937589

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.