Evidence map›Paper›PMID 37878481›Full record

ReviewExpert review of vaccines

Vaccine approaches for antigen capture by liposomes.

Shiqi Zhou, Yuan Luo, Jonathan F Lovell

Open access · diamondAbstract readReview
In one paragraph

Review in Expert review of vaccines. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

23 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Solid-Phase Glycolipid Synthesis Expedites Liposome Functionalization.Journal of the American Chemical Society · 2026
    Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Immunogenicity ofVaccines · 2026
    Article
  8. Article
  9. LiposomalCancer science · 2025
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Nanovaccines empowering CD8Theranostics · 2025
    Review
  16. Review
  17. Review
  18. Review
  19. Article
  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

3 authors at 1 institution in 1 country.

Shiqi ZhouDepartment of Biomedical Engineering, University at Buffalo, State University of New York, Buffalo, NY, USA.
Yuan LuoDepartment of Biomedical Engineering, University at Buffalo, State University of New York, Buffalo, NY, USA.
Jonathan F LovellDepartment of Biomedical Engineering, University at Buffalo, State University of New York, Buffalo, NY, USA.
University at Buffalo, State University of New York · US

Funding

Rationally-Designed, Spontaneous-Particleized Pfs48/45 for a Multivalent Malaria VaccineR01AI148557 · NIAID · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI JULIEN, JEAN-PHILIPPE, LOVELL, JONATHAN F · 2020 to 2024
$2.1M
A Cobalt Porphyrin Nanoliposome Adjuvant for MHC-I-Restricted Cancer Peptide VaccinesR01CA247771 · NCI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI ABRAMS, SCOTT I., LOVELL, JONATHAN F · 2020 to 2024
$1.9M
Developing a Multivalent Subunit Particle Vaccine Against TuberculosisR61AI169199 · NIAID · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI LOVELL, JONATHAN F, OBREGON, ANDRES · 2022 to 2024
$1.4M
NCI NIH HHS R01 CA247771NIAID NIH HHS R01 AI148557NIAID NIH HHS R61 AI169199
6 · The paper itself

Abstract

introductionLiposomes have been used as carriers for vaccine adjuvants and antigens due to their inherent biocompatibility and versatility as delivery vehicles. Two vial admixture of protein antigens with liposome-formulated immunostimulatory adjuvants has become a broadly used clinical vaccine preparation approach. Compared to freely soluble antigens, liposome-associated forms can enhance antigen delivery to antigen-presenting cells and co-deliver antigens with adjuvants, leading to improved vaccine efficacy. AREAS COVERED: Several antigen-capture strategies for liposomal vaccines have been developed for proteins, peptides, and nucleic acids. Specific antigen delivery methodologies are discussed, including electrostatic adsorption, encapsulation inside the liposome aqueous core, and covalent and non-covalent antigen capture. EXPERT OPINION: Several commercial vaccines include active lipid components, highlighting an increasingly prominent role of liposomes and lipid nanoparticles in vaccine development. Utilizing liposomes to associate antigens offers potential advantages, including antigen and adjuvant dose-sparing, co-delivery of antigen and adjuvant to immune cells, and enhanced immunogenicity. Antigen capture by liposomes has demonstrated feasibility in clinical testing. New antigen-capture techniques have been developed and appear to be of interest for vaccine development.

Indexed as

LiposomesVaccinesAdjuvants, ImmunologicAntigen-Presenting CellsAntigensHumansAdjuvants, ImmunologicAntigensLiposomesVaccinesadjuvantantigenbilayerlipopeptidesLiposomesMonophosphoryl lipid aphospholipidsQS-21

Identifiers

PMID37878481
PMCPMC10872528
OpenAlexW4387935658

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.