Evidence map›Paper›PMID 31527460›Full record

ArticleVaccines2019

Immunological Analysis of a CCHFV mRNA Vaccine Candidate in Mouse Models.

Touraj Aligholipour Farzani, Katalin Földes, Koray Ergünay, Hakan Gurdal, Aliye Bastug, Aykut Ozkul

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.6field-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

34 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
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  5. Promising Vaccine Formulations for Emerging Infectious Diseases.International journal of molecular sciences · 2025
    Review
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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

6 authors at 3 institutions in 1 country.

Touraj Aligholipour FarzaniVirology Department, Faculty of Veterinary Medicine, Ankara University, 06110 Ankara, Turkey. touraj.farzani@gmail.com.ORCID 0000-0002-1392-4048
Katalin FöldesVirology Department, Faculty of Veterinary Medicine, Ankara University, 06110 Ankara, Turkey. fldeskatalin@gmail.com.ORCID 0000-0001-6406-8168
Koray ErgünayVirology Unit, Department of Medical Microbiology, Faculty of Medicine, Hacettepe University, 06100 Ankara, Turkey. ekoray@hacettepe.edu.tr.ORCID 0000-0001-5422-1982
Hakan GurdalPharmacology Department, Faculty of Medicine, Ankara University, 06100 Ankara, Turkey. Hakan.Gurdal@medicine.ankara.edu.tr.
Aliye BastugInfectious Disease Department, Ankara Numune Training and Research Hospital, 06800 Ankara, Turkey. dr.aliye@yahoo.com.
Aykut OzkulVirology Department, Faculty of Veterinary Medicine, Ankara University, 06110 Ankara, Turkey. ozkul@ankara.edu.tr.ORCID 0000-0001-5008-9443
Ankara University · TRAnkara Numune Eğitim ve Araştırma Hastanesi · TRHacettepe University · TR

Funding

The Scientific and Technological Research Council of Turkey (TÜBİTAK) SBAG115S074
6 · The paper itself

Abstract

Development of new vaccine platforms against viral diseases is considered urgent. In recent years, mRNA constructs have attracted great interest in this field due to unique advantages over conventional gene transfer platforms. In the present study, we developed a new naked conventional mRNA vaccine expressing the non-optimized small (S) segment of the Ank-2 strain of Crimean-Congo Hemorrhagic Fever virus (CCHFV). We then analyzed its single and booster dose immunogenicity and protection potential in the challenge assay in two mice models, including IFNα/β/γR

Indexed as

CCHFVconventional naked mRNAIFNα/β/γR−/−specific immune responses

Identifiers

PMID31527460
PMCPMC6789841
OpenAlexW2974704622

What OpenQuestion 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 OpenQuestion graph.