Evidence map›Paper›PMID 29981801›Full record

ReviewAdvanced drug delivery reviews2019

Bacteriophage T4 nanoparticles for vaccine delivery against infectious diseases.

Pan Tao, Jingen Zhu, Marthandan Mahalingam, Himanshu Batra, Venigalla B Rao

Abstract readReview
In one paragraph

Review in Advanced drug delivery reviews, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
9.5field-weighted citation impact, top 2% 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

56 citing papers in PubMed, 128 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. The gut microbiota in cancer immunity and immunotherapy.Cellular & molecular immunology · 2025
    Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Current status of clinical trials for phage therapy.Journal of medical microbiology · 2024
    Review
  15. Review
  16. Designing molecules: directing stem cell differentiation.Frontiers in bioengineering and biotechnology · 2024
    Review
  17. Bacteriophage Virus-Like Particles: Platforms for Vaccine Design.Methods in molecular biology (Clifton, N.J.) · 2024
    Review
  18. Review
  19. Review
  20. 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

5 authors at 2 institutions in 2 countries.

Pan TaoDepartment of Biology, The Catholic University of America, Washington, DC 20064, USA; College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, Hubei 430070, China. Electronic address: tao.pan83@gmail.com.
Jingen ZhuDepartment of Biology, The Catholic University of America, Washington, DC 20064, USA.
Marthandan MahalingamDepartment of Biology, The Catholic University of America, Washington, DC 20064, USA.
Himanshu BatraDepartment of Biology, The Catholic University of America, Washington, DC 20064, USA.
Venigalla B RaoDepartment of Biology, The Catholic University of America, Washington, DC 20064, USA. Electronic address: rao@cua.edu.
Catholic University of America · USUniversity of America · US

Funding

Structural studies of bacteriophage T4 and their potential medical applicationsR01AI081726 · NIAID · PURDUE UNIVERSITY · PI KUHN, RICHARD J., RAO, VENIGALLA B. · 2010 to 2019
$6.2M
Identification of New Antigens for a Plague VaccineR01AI064389 · NIAID · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI CHOPRA, ASHOK K · 2005 to 2015
$3.8M
Single Dose, Multivalent, Anthrax Plague Vaccines using Bacteriophage T4 NanopartR01AI111538 · NIAID · CATHOLIC UNIVERSITY OF AMERICA · PI RAO, VENIGALLA B. · 2014 to 2018
$3.6M
A Multicomponent Anthrax Vaccine using Phage T4 DisplayU01AI056443 · NIAID · CATHOLIC UNIVERSITY OF AMERICA · PI RAO, VENIGALLA B. · 2003 to 2007
$3.3M
Multivalent Plague, Anthrax Vaccines Using Bacteriophage T4 DisplayU01AI082086 · NIAID · CATHOLIC UNIVERSITY OF AMERICA · PI RAO, VENIGALLA B. · 2009 to 2013
$2.2M
Structural studies of bacteriophage T4 and their potential medical applicationsR56AI081726 · NIAID · PURDUE UNIVERSITY · PI ROSSMANN, MICHAEL G · 2009 to 2009
$600k
NIAID NIH HHS R01 AI064389NIAID NIH HHS R01 AI081726NIAID NIH HHS R01 AI111538NIAID NIH HHS R56 AI081726NIAID NIH HHS U01 AI056443NIAID NIH HHS U01 AI082086
6 · The paper itself

Abstract

Subunit vaccines containing one or more target antigens from pathogenic organisms represent safer alternatives to whole pathogen vaccines. However, the antigens by themselves are not sufficiently immunogenic and require additives known as adjuvants to enhance immunogenicity and protective efficacy. Assembly of the antigens into virus-like nanoparticles (VLPs) is a better approach as it allows presentation of the epitopes in a more native context. The repetitive, symmetrical, and high density display of antigens on the VLPs mimic pathogen-associated molecular patterns seen on bacteria and viruses. The antigens, thus, might be better presented to stimulate host's innate as well as adaptive immune systems thereby eliciting both humoral and cellular immune responses. Bacteriophages such as phage T4 provide excellent platforms to generate the nanoparticle vaccines. The T4 capsid containing two non-essential outer proteins Soc and Hoc allow high density array of antigen epitopes in the form of peptides, domains, full-length proteins, or even multi-subunit complexes. Co-delivery of DNAs, targeting molecules, and/or molecular adjuvants provides additional advantages. Recent studies demonstrate that the phage T4 VLPs are highly immunogenic, do not need an adjuvant, and provide complete protection against bacterial and viral pathogens. Thus, phage T4 could potentially be developed as a "universal" VLP platform to design future multivalent vaccines against complex and emerging pathogens.

Indexed as

Bacteriophage T4Phage TherapyAnimalsCommunicable DiseasesHumansNanoparticlesVaccines, Virus-Like ParticleVaccines, Virus-Like ParticleBacteriophage T4DNA packagingPhage assemblyPhage displayVaccinesVirus like particle

Identifiers

PMID29981801
PMCPMC6759415
OpenAlexW2833821224

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.