Evidence map›Paper›PMID 19601838›Full record

ReviewCurrent pharmaceutical design2009

The roles of antimicrobial peptides in innate host defense.

Gill Diamond, Nicholas Beckloff, Aaron Weinberg, Kevin O Kisich

Open access · bronzeAbstract readReview
In one paragraph

Review in Current pharmaceutical design, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 305 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
305citing papers in PubMed, 2 pooled it
18.7field-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

305 citing papers in PubMed, 2 syntheses or guidelines pooled it, 627 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Review
  6. Lipoteichoic Acid Fraction fromMicroorganisms · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Isolation of Fusobacterium nucleatum-Induced Host Exosomal sRNAs.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Synthetic host defense peptide inhibits SARS-CoV-2 replicationAntimicrobial agents and chemotherapy · 2025
    Article

245 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 2 institutions in 1 country.

Gill DiamondDepartment of Oral Biology, UMDNJ-New Jersey Dental School, Newark, NJ 07101, USA. gdiamond@umdnj.edu
Nicholas Beckloff
Aaron Weinberg
Kevin O Kisich
Rutgers, The State University of New Jersey · USUniversity of Colorado Denver · US

Funding

Ontogeny Of Oral Epithelial Antimicrobial PeptidesR01DE018276 · NIDCR · CASE WESTERN RESERVE UNIVERSITY · PI WEINBERG, AARON · 2007 to 2015
$3.5M
Bacteria-host cell interactions in periodontal diseaseR01DE014897 · NIDCR · UNIV OF MED/DENT OF NJ-NJ DENTAL SCHOOL · PI DIAMOND, GILL · 2002 to 2005
$1.6M
Oral Mucosal Beta Defensins and HIVR01DE015510 · NIDCR · CASE WESTERN RESERVE UNIVERSITY · PI WEINBERG, AARON · 2003 to 2006
$1.5M
B-defensin protection of human oral epithelial cellsR01DE016334 · NIDCR · CASE WESTERN RESERVE UNIVERSITY · PI WEINBERG, AARON · 2005 to 2008
$1.4M
Host-Pathogen Interactions in the Mammalian AirwayR01HL067871 · NHLBI · UNIV OF MED/DENT OF NJ-NJ DENTAL SCHOOL · PI DIAMOND, GILL · 2003 to 2006
$1.2M
Defense of oral epithelial cells from candida by hBDsR01DE017334 · NIDCR · CASE WESTERN RESERVE UNIVERSITY · PI WEINBERG, AARON · 2005 to 2007
$791k
Vitamin D induction of antibacterial activity in gingival cellsR21DE018781 · NIDCR · UNIV OF MED/DENT OF NJ-NJ DENTAL SCHOOL · PI DIAMOND, GILL · 2008 to 2009
$446k
Antimicrobial Peptides in Resistance to TuberculosisR21AI052316 · NIAID · NATIONAL JEWISH HEALTH · PI KISICH, KEVIN O · 2002 to 2002
$256k
NHLBI NIH HHS R01 HL067871NHLBI NIH HHS R01 HL67871NIAID NIH HHS R21 AI52316NIDCR NIH HHS R01 DE014897NIDCR NIH HHS R01 DE015510NIDCR NIH HHS R01 DE016334NIDCR NIH HHS R01 DE017334NIDCR NIH HHS R01 DE018276NIDCR NIH HHS R01DE14897NIDCR NIH HHS R01DE15510NIDCR NIH HHS R01 DE16334NIDCR NIH HHS R01 DE17334NIDCR NIH HHS R01 DE18276NIDCR NIH HHS R21 DE018781
6 · The paper itself

Abstract

Antimicrobial peptides (AMPs) are multi-functional peptides whose fundamental biological role in vivo has been proposed to be the elimination of pathogenic microorganisms, including Gram-positive and -negative bacteria, fungi, and viruses. Genes encoding these peptides are expressed in a variety of cells in the host, including circulating phagocytic cells and mucosal epithelial cells, demonstrating a wide range of utility in the innate immune system. Expression of these genes is tightly regulated; they are induced by pathogens and cytokines as part of the host defense response, and they can be suppressed by bacterial virulence factors and environmental factors which can lead to increased susceptibility to infection. New research has also cast light on alternative functionalities, including immunomodulatory activities, which are related to their unique structural characteristics. These peptides represent not only an important component of innate host defense against microbial colonization and a link between innate and adaptive immunity, but also form a foundation for the development of new therapeutic agents.

Indexed as

Adaptive ImmunityAnimalsAnti-Infective AgentsAntimicrobial Cationic PeptidesHumansImmunity, InnateAnti-Infective AgentsAntimicrobial Cationic Peptides

Identifiers

PMID19601838
PMCPMC2750833
OpenAlexW2147574532

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.