Evidence map›Paper›PMID 32807876›Full record

ReviewNature nanotechnology2021

Advances in nanomaterial vaccine strategies to address infectious diseases impacting global health.

Chelsea N Fries, Elizabeth J Curvino, Jui-Lin Chen, Sallie R Permar, Genevieve G Fouda, Joel H Collier

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature nanotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 98 papers.

0numbers the graph read from it
0cells of the map it votes in
98citing 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

98 citing papers in PubMed.

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  11. Review
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  13. Hantavirus GnACS infectious diseases · 2025
    Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Flexing protein assemblies.Nature structural & molecular biology · 2025
    Article
  19. A basedMaterials today. Bio · 2025
    Article
  20. Article

38 more citing papers are in PubMed but not listed here.

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

6 authors.

Chelsea N Fries *Department of Biomedical Engineering, Duke University, Durham, NC, USA.
Elizabeth J Curvino *Department of Biomedical Engineering, Duke University, Durham, NC, USA.ORCID http://orcid.org/0000-0003-4452-0457
Jui-Lin ChenDepartment of Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, NC, USA.ORCID http://orcid.org/0000-0002-7646-4907
Sallie R PermarDepartment of Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, NC, USA.ORCID http://orcid.org/0000-0003-1438-4554
Genevieve G FoudaDepartment of Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, NC, USA. genevieve.fouda@duke.edu.ORCID http://orcid.org/0000-0002-0960-1019
Joel H CollierDepartment of Biomedical Engineering, Duke University, Durham, NC, USA. joel.collier@duke.edu.ORCID http://orcid.org/0000-0003-3536-4827

Funding

Modular Self-Assembled Coatings for BiomaterialsR01EB009701 · NIBIB · UNIVERSITY OF CHICAGO · PI COLLIER, JOEL H · 2009 to 2021
$4.3M
Supramolecular pediatric HIV vaccine designR01AI145016 · NIAID · DUKE UNIVERSITY · PI COLLIER, JOEL H, FOUDA AMOU OU, GENEVIEVE GINY · 2019 to 2022
$3.1M
NIAID NIH HHS R01 AI145016NIBIB NIH HHS R01 EB009701
6 · The paper itself

Abstract

Despite the overwhelming success of vaccines in preventing infectious diseases, there remain numerous globally devastating diseases without fully protective vaccines, particularly human immunodeficiency virus (HIV), malaria and tuberculosis. Nanotechnology approaches are being developed both to design new vaccines against these diseases as well as to facilitate their global implementation. The reasons why a given pathogen may present difficulties for vaccine design are unique and tied to the co-evolutionary history of the pathogen and humans, but there are common challenges that nanotechnology is beginning to help address. In each case, a successful vaccine will need to raise immune responses that differ from the immune responses raised by normal infection. Nanomaterials, with their defined compositions, commonly modular construction, and length scales allowing the engagement of key immune pathways, collectively facilitate the iterative design process necessary to identify such protective immune responses and achieve them reliably. Nanomaterials also provide strategies for engineering the trafficking and delivery of vaccine components to key immune cells and lymphoid tissues, and they can be highly multivalent, improving their engagement with the immune system. This Review will discuss these aspects along with recent nanomaterial advances towards vaccines against infectious disease, with a particular emphasis on HIV/AIDS, malaria and tuberculosis.

Indexed as

NanotechnologyBiomedical ResearchCommunicable DiseasesGlobal HealthHumansImmunityMalariaNanostructuresTuberculosisVaccinesVaccines

Identifiers

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.