Evidence map›Paper›PMID 34512658›Full record

ArticleFrontiers in immunology2021

Impact of Toll-Like Receptor-Specific Agonists on the Host Immune Response to the

Sergei Biryukov, Jennifer L Dankmeyer, Zain Shamsuddin, Ivan Velez, Nathaniel O Rill, Raysa Rosario-Acevedo, Christopher P Klimko, Jennifer L Shoe, Melissa Hunter, Michael D Ward and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Anti-infective compounds forSustainable microbiology · 2026
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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

16 authors at 1 institution in 1 country.

Sergei BiryukovBacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Jennifer L DankmeyerBacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Zain ShamsuddinBacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Ivan VelezBacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Nathaniel O RillBacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Raysa Rosario-AcevedoBacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Christopher P KlimkoBacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Jennifer L ShoeBacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Melissa HunterBacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Michael D WardMolecular Biology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Lisa H CazaresMolecular Biology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
David P FettererBiostatistics Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Joel A BozueBacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Patricia L WorshamBacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Christopher K CoteBacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
Kei AmemiyaBacteriology Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, MD, United States.
United States Army Medical Research Institute of Infectious Diseases · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Relatively recent advances in plague vaccinology have produced the recombinant fusion protein F1-V plague vaccine. This vaccine has been shown to readily protect mice from both bubonic and pneumonic plague. The protection afforded by this vaccine is solely based upon the immune response elicited by the F1 or V epitopes expressed on the F1-V fusion protein. Accordingly, questions remain surrounding its efficacy against infection with non-encapsulated (F1-negative) strains. In an attempt to further optimize the F1-V elicited immune response and address efficacy concerns, we examined the inclusion of multiple toll-like receptor agonists into vaccine regimens. We examined the resulting immune responses and also any protection afforded to mice that were exposed to aerosolized

Indexed as

Adjuvants, ImmunologicAnimalsAntigens, BacterialFemaleMiceMice, Inbred BALB CPlaguePlague VaccineToll-Like ReceptorsVaccinationVaccine EfficacyVaccines, SyntheticYersinia pestisAdjuvants, ImmunologicAntigens, BacterialPlague VaccineToll-Like ReceptorsVaccines, SyntheticCpGF1-V antigenimmune responsemiceplaguetoll-like receptorsvaccineYersinia pestis

Identifiers

PMID34512658
PMCPMC8430260
OpenAlexW3196990457

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.