Evidence map›Paper›PMID 27076136›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2016

Development of a SARS Coronavirus Vaccine from Recombinant Spike Protein Plus Delta Inulin Adjuvant.

Clifton McPherson, Richard Chubet, Kathy Holtz, Yoshikazu Honda-Okubo, Dale Barnard, Manon Cox, Nikolai Petrovsky

Abstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed, 33 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review on Approved and Inprogress COVID-19 Vaccines.Iranian journal of pharmaceutical research : IJPR · 2022
    Review
  5. A comparison between SARS-CoV-1 and SARS-CoV2: an update on current COVID-19 vaccines.Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences · 2022
    Review
  6. Review
  7. Review
  8. Article
  9. Nanotherapeutics for treating coronavirus diseases.Journal of drug delivery science and technology · 2021
    Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Adjuvants for Coronavirus Vaccines.Frontiers in immunology · 2020
    Review
  15. Coronaviruses: An Updated Overview of Their Replication and Pathogenesis.Methods in molecular biology (Clifton, N.J.) · 2020
    Review
  16. Article
  17. Review
  18. Article
  19. 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 4 institutions in 2 countries.

Clifton McPhersonProtein Sciences Corporation Inc, Meriden, CT, USA.
Richard ChubetProtein Sciences Corporation Inc, Meriden, CT, USA.
Kathy HoltzProtein Sciences Corporation Inc, Meriden, CT, USA.
Yoshikazu Honda-OkuboVaxine Pty Ltd, 1 Flinders Drive, Bedford Park, Adelaide, 5042, Australia.
Dale BarnardInstitute for Antiviral Research, Utah State University, 5600 Old Main Hill, Logan, UT, 84322-560, USA.
Manon CoxProtein Sciences Corporation Inc, Meriden, CT, USA.
Nikolai PetrovskyVaxine Pty Ltd, 1 Flinders Drive, Bedford Park, Adelaide, 5042, Australia. nikolai.petrovsky@flinders.edu.au.
MSM Protein Technologies (United States) · USFlinders University · AUUtah State University · USVaxine (Australia) · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Given periodic outbreaks of fatal human infections caused by coronaviruses, development of an optimal coronavirus vaccine platform capable of rapid production is an ongoing priority. This chapter describes the use of an insect cell expression system for rapid production of a recombinant vaccine against severe acute respiratory syndrome coronavirus (SARS). Detailed methods are presented for expression, purification, and release testing of SARS recombinant spike protein antigen, followed by adjuvant formulation and animal testing. The methods herein described for rapid development of a highly protective SARS vaccine are equally suited to rapid development of vaccines against other fatal human coronavirus infections, e.g., the MERS coronavirus.

Indexed as

Adjuvants, ImmunologicAnimalsHumansInulinSevere Acute Respiratory SyndromeSevere acute respiratory syndrome-related coronavirusSpike Glycoprotein, CoronavirusViral VaccinesAdjuvants, ImmunologicInulinSpike Glycoprotein, CoronavirusViral VaccinesAdjuvantAdvax adjuvantBaculoviruscGMPCoronavirusDelta inulinManufactureMERSSARSVaccine

Identifiers

PMID27076136
PMCPMC7139448
OpenAlexW2473724487

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.