Evidence map›Paper›PMID 35667222›Full record

ReviewCurrent opinion in immunology2022

Bioinspired vaccines to enhance MHC class-I antigen cross-presentation.

Jessalyn J Baljon, John T Wilson

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in immunology, 2022. 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
3.3field-weighted citation impact, top 6% 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, 40 citations in OpenAlex.

  1. Trial
  2. Review
  3. Design Considerations for Potent DNA-Platform-Based Cancer Vaccines.Current opinion in biomedical engineering · 2026
    Article
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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

2 authors at 1 institution in 1 country.

Jessalyn J BaljonDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA.
John T WilsonDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA; Department of Chemical and Biomolecular Engineering, Vanderbilt University, Nashville, TN 37235, USA; Vanderbilt Institute for Infection, Immunology, and Inflammation, Vanderbilt University Medical Center, Nashville, TN 37232, USA; Vanderbilt Institute of Chemical Biology, Vanderbilt University Medical Center, Nashville, TN 37232, USA; Vanderbilt Center for Immunobiology, Vanderbilt University Medical Center, Nashville, TN 37232, USA; Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, TN 37232, USA. Electronic address: john.t.wilson@vanderbilt.edu.
Vanderbilt University · US

Funding

Expanding the Therapeutic Window of Nanoparticle STING Agonists for Cancer ImmunotherapyR01CA245134 · NCI · VANDERBILT UNIVERSITY · PI WILSON, JOHN TANNER · 2020 to 2025
$1.8M
An Engineered Nanocarrier Platform for Enhancing Immune Responses to Neoantigen-Targeted Cancer VaccinesF31CA257275 · NCI · VANDERBILT UNIVERSITY · PI BALJON, JESSALYN J · 2021 to 2023
$120k
Vaccinating at Mucosal Surfaces with Nanoparticle Conjugated Antigen and AdjuvantI01BX001444 · VA · VETERANS HEALTH ADMINISTRATION · PI JOYCE, SEBASTIAN · 2014 to 2022
–
BLRD VA I01 BX001444NCI NIH HHS F31 CA257275NCI NIH HHS R01 CA245134
6 · The paper itself

Abstract

Cross-presentation of exogenous antigen on MHC class-I is a crucial process for generating a CD8

Indexed as

Cross-PrimingVaccinesAdjuvants, ImmunologicAntigen PresentationAntigensCD8-Positive T-LymphocytesDendritic CellsHistocompatibility Antigens Class IHumansAdjuvants, ImmunologicAntigensHistocompatibility Antigens Class IVaccines

Identifiers

PMID35667222
PMCPMC9695705
OpenAlexW4281746438

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.