Evidence map›Paper›PMID 30089512›Full record

ArticleVirology journal2018

Human β-defensin 2 plays a regulatory role in innate antiviral immunity and is capable of potentiating the induction of antigen-specific immunity.

Ju Kim, Ye Lin Yang, Sun-Hee Jang, Yong-Suk Jang

Open access · goldAbstract read
In one paragraph

Article in Virology journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed
9.3field-weighted citation impact, top 1% 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

91 citing papers in PubMed, 148 citations in OpenAlex.

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  2. Proteome conserved multi-epitope-based vaccine construct against Nipah virus.Naunyn-Schmiedeberg's archives of pharmacology · 2026
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31 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 1 country.

Ju KimDepartment of Molecular Biology and the Institute for Molecular Biology and Genetics, Chonbuk National University, Jeonju, 54896, Korea.
Ye Lin YangDepartment of Bioactive Material Sciences and Institute of Bioactive Materials, Chonbuk National University, Jeonju, 54896, Korea.
Sun-Hee JangDepartment of Molecular Biology and the Institute for Molecular Biology and Genetics, Chonbuk National University, Jeonju, 54896, Korea.
Yong-Suk JangDepartment of Molecular Biology and the Institute for Molecular Biology and Genetics, Chonbuk National University, Jeonju, 54896, Korea. yongsuk@jbnu.ac.kr.ORCID 0000-0002-1675-4224
Jeonbuk National University · KR

Funding

Korea National Research Counsil of Science & Technology CRC-16-01-KRICT
6 · The paper itself

Abstract

backgroundAntimicrobial peptides (AMPs) are primarily known for their innate immune defense against invading microorganisms, including viruses. In addition, recent research has suggested their modulatory activity in immune induction. Given that most subunit vaccines require an adjuvant to achieve effective immune induction through the activation of innate immunity, AMPs are plausible candidate molecules for stimulating not only innate immune but also adaptive immune responses.

resultsIn this study, we investigated the ability of human β-defensin (HBD) 2 to promote antiviral immunity in vitro and in vivo using a receptor-binding domain (RBD) of Middle East respiratory syndrome-coronavirus (MERS-CoV) spike protein (S RBD) as a model antigen (Ag). When HBD 2-conjugated S RBD was used to treat THP-1 human monocytic cells, the expression levels of antiviral (IFN-β, IFN-γ, MxA, PKR, and RNaseL) and primary immune-inducing (NOD2, TNF-α, IL-1β, and IL-6) molecules were enhanced compared to those expressed after treatment with S RBD only. The expression of chemokines capable of recruiting leukocytes, including monocytes/macrophages, natural killer cells, granulocytes, T cells, and dendritic cells, was also increased following HBD 2-conjugated S RBD treatment. More important, immunization of mice with HBD 2-conjugated S RBD enhanced the immunogenicity of the S RBD and elicited a higher S RBD-specific neutralizing antibody response than S RBD alone.

conclusionsWe conclude that HBD 2 activates the primary antiviral innate immune response and may also mediate the induction of an effective adaptive immune response against a conjugated Ag.

Indexed as

Adaptive ImmunityAdjuvants, ImmunologicAnimalsAntibodies, NeutralizingAntibodies, ViralAntigens, ViralAntiviral Agentsbeta-DefensinsCell Line, TumorChlorocebus aethiopsCoronavirus InfectionsFemaleHumansImmunity, InnateMacrophagesMiceAdjuvants, ImmunologicAntibodies, NeutralizingAntibodies, ViralAntigens, ViralAntiviral Agentsbeta-DefensinsDEFB4A protein, humanSpike Glycoprotein, CoronavirusVaccines, SubunitViral VaccinesAdjuvantAntibodyAntigenHuman β-defensinMERS-CoV

Identifiers

PMID30089512
PMCPMC6083524
OpenAlexW2886789714

What OpenQuestion holds

Textmetadata
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.