Evidence map›Paper›PMID 30076864›Full record

ArticleAntiviral research2018

LL-37 disrupts the Kaposi's sarcoma-associated herpesvirus envelope and inhibits infection in oral epithelial cells.

David C Brice, Zsolt Toth, Gill Diamond

Open access · bronzeAbstract read
In one paragraph

Article in Antiviral research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.5field-weighted citation impact, top 8% 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

28 citing papers in PubMed, 69 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Immune Modulatory Effects of Vitamin D on Herpesvirus Infections.International journal of molecular sciences · 2025
    Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. The Role of Antimicrobial Peptides in Preterm Birth.International journal of molecular sciences · 2021
    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.

David C BriceDepartment of Oral Biology, University of Florida, Box 100424, Gainesville, FL, 32610, USA.
Zsolt TothDepartment of Oral Biology, University of Florida, Box 100424, Gainesville, FL, 32610, USA; UF Genetics Institute, Gainesville, FL, 32610, USA; UF Health Cancer Center, Gainesville, FL, 32610, USA.
Gill DiamondDepartment of Oral Biology, University of Florida, Box 100424, Gainesville, FL, 32610, USA. Electronic address: gdiamond@dental.ufl.edu.
University of Florida · US

Funding

Comprehensive Training Program in Oral BiologyT90DE021990 · NIDCR · UNIVERSITY OF FLORIDA · PI Jose A Lemos · 2011 to 2026
$8.2M
Viral and host strategies for regulation of KSHV infectionR01AI132554 · NIAID · UNIVERSITY OF FLORIDA · PI TOTH, ZSOLT · 2018 to 2022
$1.9M
Vitamin D and Periodontal DiseaseR01DE022723 · NIDCR · UNIV OF MED/DENT OF NJ-NJ DENTAL SCHOOL · PI DIAMOND, GILL · 2012 to 2014
$791k
Regulation of KSHV lytic replication in oral epithelial cellsR03DE025562 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TOTH, ZSOLT · 2015 to 2016
$236k
NIAID NIH HHS R01 AI132554NIDCR NIH HHS R01 DE022723NIDCR NIH HHS R03 DE025562NIDCR NIH HHS T90 DE021990
6 · The paper itself

Abstract

Oral epithelial cells (OECs) represent the first line of defense against viruses that are spread via saliva, including Kaposi's sarcoma-associated herpesvirus (KSHV). Infection of humans by KSHV and viral pathogenesis begins by infecting OECs. One method OECs use to limit viral infections in the oral cavity is the production of antimicrobial peptides (AMPs), or host defense peptides (HDPs). However, no studies have investigated the antiviral activities of any HDP against KSHV. The goal of this study was to determine the antiviral activity of one HDP, LL-37, against KSHV in the context of infecting OECs. Our results show that LL-37 significantly decreased KSHV's ability to infect OECs in both a structure- and dose-dependent manner. However, this activity does not stem from affecting OECs, but instead the virions themselves. We found that LL-37 exerts its antiviral activity against KSHV by disrupting the viral envelope, which can inhibit viral entry into OECs. Our data suggest that LL-37 exhibits a marked antiviral activity against KSHV during infection of oral epithelial cells, which can play an important role in host defense against oral KSHV infection. Thus, we propose that inducing LL-37 expression endogenously in oral epithelial cells, or potentially introducing as a therapy, may help restrict oral KSHV infection and ultimately KSHV-associated diseases.

Indexed as

Antimicrobial Cationic PeptidesAntiviral AgentsCathelicidinsCell LineEpithelial CellsHerpesviridae InfectionsHerpesvirus 8, HumanHumansKeratinocytesMouthVirionVirus InternalizationAntimicrobial Cationic PeptidesAntiviral AgentsCathelicidinsAntimicrobial peptideGingival epitheliumHost defense peptideKSHVLL-37Saliva

Identifiers

PMID30076864
PMCPMC6383517
OpenAlexW2885166080

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.