Evidence map›Paper›PMID 33955657›Full record

ArticleJournal of biomedical materials research. Part A2021

Modulation of injectable hydrogel properties for slow co-delivery of influenza subunit vaccine components enhance the potency of humoral immunity.

Olivia M Saouaf, Gillie A Roth, Ben S Ou, Anton A A Smith, Anthony C Yu, Emily C Gale, Abigail K Grosskopf, Vittoria C T M Picece, Eric A Appel

Open access · hybridAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.7field-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

22 citing papers in PubMed, 45 citations in OpenAlex.

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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

9 authors at 3 institutions in 3 countries.

Olivia M SaouafDepartment of Materials Science & Engineering, Stanford University, Stanford, California, USA.ORCID 0000-0002-5117-7127
Gillie A RothDepartment of Bioengineering, Stanford University, Stanford, California, USA.ORCID 0000-0002-3451-3694
Ben S OuDepartment of Bioengineering, Stanford University, Stanford, California, USA.ORCID 0000-0002-0539-5166
Anton A A SmithDepartment of Materials Science & Engineering, Stanford University, Stanford, California, USA.
Anthony C YuDepartment of Materials Science & Engineering, Stanford University, Stanford, California, USA.ORCID 0000-0002-5888-2718
Emily C GaleDepartment of Biochemistry, Stanford University School of Medicine, Stanford, California, USA.ORCID 0000-0002-6536-3027
Abigail K GrosskopfDepartment of Chemical Engineering, Stanford University, Stanford, California, USA.ORCID 0000-0002-0471-1825
Vittoria C T M PiceceDepartment of Materials Science & Engineering, Stanford University, Stanford, California, USA.
Eric A AppelDepartment of Materials Science & Engineering, Stanford University, Stanford, California, USA.ORCID 0000-0002-2301-7126
Stanford University · USETH Zurich · CHInstitute of Infection and Immunity · CA

Funding

Supplement to Enhance Wellness and Resiliency in the Graduate EnvironmentT32GM007276 · NIGMS · STANFORD UNIVERSITY · PI MORRISON, ASHBY J. · 1985 to 2023
$32.9M
Gates Foundation OPP1113682Gates Foundation OPP1211043NIGMS NIH HHS T32 GM007276NIH HHS T32 GM007276
6 · The paper itself

Abstract

Vaccines are critical for combating infectious diseases across the globe. Influenza, for example, kills roughly 500,000 people annually worldwide, despite annual vaccination campaigns. Efficacious vaccines must elicit a robust and durable antibody response, and poor efficacy often arises from inappropriate temporal control over antigen and adjuvant presentation to the immune system. In this work, we sought to exploit the immune system's natural response to extended pathogen exposure during infection by designing an easily administered slow-delivery influenza vaccine platform. We utilized an injectable and self-healing polymer-nanoparticle (PNP) hydrogel platform to prolong the co-delivery of vaccine components to the immune system. We demonstrated that these hydrogels exhibit unique dynamic physical characteristics whereby physicochemically distinct influenza hemagglutinin antigen and a toll-like receptor 7/8 agonist adjuvant could be co-delivered over prolonged timeframes that were tunable through simple alteration of the gel formulation. We show a relationship between hydrogel physical properties and the resulting immune response to immunization. When administered in mice, hydrogel-based vaccines demonstrated enhancements in the magnitude and duration of humoral immune responses compared to alum, a widely used clinical adjuvant system. We found stiffer hydrogel formulations exhibited slower release and resulted in the greatest improvements to the antibody response while also enabling significant adjuvant dose sparing. In summary, this work introduces a simple and effective vaccine delivery platform that increases the potency and durability of influenza subunit vaccines.

Indexed as

Adjuvants, ImmunologicDelayed-Action PreparationsHydrogelsImmunity, HumoralInfluenza VaccinesAnimalsMiceVaccines, SubunitAdjuvants, ImmunologicDelayed-Action PreparationsHydrogelsInfluenza VaccinesVaccines, Subunitbiomaterialshydrogelsimmunoengineeringinfectious diseasevaccines

Identifiers

PMID33955657
PMCPMC8518857
OpenAlexW3157360403

What Socratic 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 Socratic graph.