Evidence map›Paper›PMID 24441019›Full record

ArticleScientific reports2014

A systems approach to designing next generation vaccines: combining α-galactose modified antigens with nanoparticle platforms.

Yashdeep Phanse, Brenda R Carrillo-Conde, Amanda E Ramer-Tait, Scott Broderick, Chang Sun Kong, Krishna Rajan, Ramon Flick, Robert B Mandell, Balaji Narasimhan, Michael J Wannemuehler

Abstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
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

18 citing papers in PubMed.

  1. Article
  2. Cell-free systems for accelerating glycoprotein expression and biomanufacturing.Journal of industrial microbiology & biotechnology · 2020
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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

10 authors.

Yashdeep Phanse1] Department of Veterinary Microbiology and Preventive Medicine, Iowa State University, Ames, IA 50011 [2].
Brenda R Carrillo-Conde1] Department of Chemical and Biological Engineering, Iowa State University, Ames, IA 50011 [2].
Amanda E Ramer-Tait1] Department of Veterinary Microbiology and Preventive Medicine, Iowa State University, Ames, IA 50011 [2] Department of Food Science and Technology, University of Nebraska-Lincoln, Lincoln, NE 68583.
Scott BroderickDepartment of Materials Science and Engineering, Iowa State University, Ames, IA 50011.
Chang Sun KongDepartment of Materials Science and Engineering, Iowa State University, Ames, IA 50011.
Krishna RajanDepartment of Materials Science and Engineering, Iowa State University, Ames, IA 50011.
Ramon FlickBioProtection Systems Corporation, a subsidiary of NewLink Genetics Corporation, Ames, IA 50010.
Robert B Mandell1] BioProtection Systems Corporation, a subsidiary of NewLink Genetics Corporation, Ames, IA 50010 [2].
Balaji NarasimhanDepartment of Chemical and Biological Engineering, Iowa State University, Ames, IA 50011.
Michael J WannemuehlerDepartment of Veterinary Microbiology and Preventive Medicine, Iowa State University, Ames, IA 50011.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Innovative vaccine platforms are needed to develop effective countermeasures against emerging and re-emerging diseases. These platforms should direct antigen internalization by antigen presenting cells and promote immunogenic responses. This work describes an innovative systems approach combining two novel platforms, αGalactose (αGal)-modification of antigens and amphiphilic polyanhydride nanoparticles as vaccine delivery vehicles, to rationally design vaccine formulations. Regimens comprising soluble αGal-modified antigen and nanoparticle-encapsulated unmodified antigen induced a high titer, high avidity antibody response with broader epitope recognition of antigenic peptides than other regimen. Proliferation of antigen-specific CD4(+) T cells was also enhanced compared to a traditional adjuvant. Combining the technology platforms and augmenting immune response studies with peptide arrays and informatics analysis provides a new paradigm for rational, systems-based design of next generation vaccine platforms against emerging and re-emerging pathogens.

Indexed as

Immunity, InnateAdjuvants, Immunologicalpha-GalactosidaseAntigen-Presenting CellsAntigensCD4-Positive T-LymphocytesEpitopesHumansNanoparticlesPeptidesSystems BiologyVaccinesAdjuvants, Immunologicalpha-GalactosidaseAntigensEpitopesPeptidesVaccines

Identifiers

PMID24441019
PMCPMC3895907

What OpenQuestion holds

Textmetadata
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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.