Evidence map›Paper›PMID 24382398›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2014

Elimination of the cold-chain dependence of a nanoemulsion adjuvanted vaccine against tuberculosis by lyophilization.

Mark T Orr, Ryan M Kramer, Lucien Barnes, Quinton M Dowling, Anthony L Desbien, Elyse A Beebe, John D Laurance, Christopher B Fox, Steven G Reed, Rhea N Coler and 1 more

Abstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
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  8. Pathological and protective roles of dendritic cells inFrontiers in cellular and infection microbiology · 2022
    Review
  9. Article
  10. Article
  11. Microparticle encapsulation of a tuberculosis subunit vaccine candidate containing a nanoemulsion adjuvant via spray drying.European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V · 2021
    Article
  12. Development of thermostable vaccine adjuvants.Expert review of vaccines · 2021
    Review
  13. Article
  14. Article
  15. Article
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  18. Review
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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 1 institution in 1 country.

Mark T OrrInfectious Disease Research Institute, Seattle, WA 98102, USA. Electronic address: mark.orr@idri.org.
Ryan M KramerInfectious Disease Research Institute, Seattle, WA 98102, USA.
Lucien BarnesInfectious Disease Research Institute, Seattle, WA 98102, USA.
Quinton M DowlingInfectious Disease Research Institute, Seattle, WA 98102, USA.
Anthony L DesbienInfectious Disease Research Institute, Seattle, WA 98102, USA.
Elyse A BeebeInfectious Disease Research Institute, Seattle, WA 98102, USA.
John D LauranceInfectious Disease Research Institute, Seattle, WA 98102, USA.
Christopher B FoxInfectious Disease Research Institute, Seattle, WA 98102, USA.
Steven G ReedInfectious Disease Research Institute, Seattle, WA 98102, USA.
Rhea N ColerInfectious Disease Research Institute, Seattle, WA 98102, USA.
Thomas S VedvickInfectious Disease Research Institute, Seattle, WA 98102, USA.
Infectious Disease Research Institute · US

Funding

Development and Manufacture of Adjuvants for Vaccines Targeting MDR TuberculosisU01AI078054 · NIAID · ACCESS TO ADVANCED HEALTH INSTITUTE · PI COLER, RHEA N · 2008 to 2011
$6.2M
NIAID NIH HHS HHSN272200800045CNIAID NIH HHS U01 AI078054NIAID NIH HHS U01AI078054
6 · The paper itself

Abstract

Next-generation rationally-designed vaccine adjuvants represent a significant breakthrough to enable development of vaccines against challenging diseases including tuberculosis, HIV, and malaria. New vaccine candidates often require maintenance of a cold-chain process to ensure long-term stability and separate vials to enable bedside mixing of antigen and adjuvant. This presents a significant financial and technological barrier to worldwide implementation of such vaccines. Herein we describe the development and characterization of a tuberculosis vaccine comprised of both antigen and adjuvant components that are stable in a single vial at sustained elevated temperatures. Further this vaccine retains the ability to elicit both antibody and TH1 responses against the vaccine antigen and protect against experimental challenge with Mycobacterium tuberculosis. These results represent a significant breakthrough in the development of vaccine candidates that can be implemented throughout the world without being hampered by the necessity of a continuous cold chain or separate adjuvant and antigen vials.

Indexed as

Adjuvants, ImmunologicAnimalsAntibodies, BacterialAntigens, BacterialBacterial LoadB-LymphocytesEmulsionsFemaleFreeze DryingLeukocyte CountLungMiceMice, Inbred C57BLMycobacterium tuberculosisNanostructuresSpleenAdjuvants, ImmunologicAntibodies, BacterialAntigens, BacterialEmulsionsTuberculosis VaccinesAdjuvantLyophilizationNanoemulsionVaccine

Identifiers

PMID24382398
PMCPMC3956454
OpenAlexW1984130714

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.