Unknown

Dataset Information

0

Identification of synthetic host defense peptide mimics that exert dual antimicrobial and anti-inflammatory activities.


ABSTRACT: A group of synthetic antimicrobial oligomers, inspired by naturally occurring antimicrobial peptides, were analyzed for the ability to modulate innate immune responses to Toll-like receptor (TLR) ligands. These synthetic mimics of antimicrobial peptides (SMAMPs) specifically reduced cytokine production in response to Staphylococcus aureus and the S. aureus component lipoteichoic acid (LTA), a TLR2 agonist. Anti-inflammatory SMAMPs prevented the induction of tumor necrosis factor (TNF), interleukin 6 (IL-6), and IL-10 in response to S. aureus or LTA, but no other TLR2 ligands. We show that these SMAMPs bind specifically to LTA in vitro and prevent its interaction with TLR2. Importantly, the SMAMP greatly reduced the induction of TNF and IL-6 in vivo in mice acutely infected with S. aureus while simultaneously reducing bacterial loads dramatically (4 log(10)). Thus, these SMAMPs can eliminate the damage induced by pathogen-associated molecular patterns (PAMPs) while simultaneously eliminating infection in vivo. They are the first known SMAMPs to demonstrate anti-inflammatory and antibacterial activities in vivo.

SUBMITTER: Som A 

PROVIDER: S-EPMC3491551 | biostudies-literature | 2012 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications

Identification of synthetic host defense peptide mimics that exert dual antimicrobial and anti-inflammatory activities.

Som Abhigyan A   Navasa Nicolás N   Percher Avital A   Scott Richard W RW   Tew Gregory N GN   Anguita Juan J  

Clinical and vaccine immunology : CVI 20120905 11


A group of synthetic antimicrobial oligomers, inspired by naturally occurring antimicrobial peptides, were analyzed for the ability to modulate innate immune responses to Toll-like receptor (TLR) ligands. These synthetic mimics of antimicrobial peptides (SMAMPs) specifically reduced cytokine production in response to Staphylococcus aureus and the S. aureus component lipoteichoic acid (LTA), a TLR2 agonist. Anti-inflammatory SMAMPs prevented the induction of tumor necrosis factor (TNF), interleuk  ...[more]

Similar Datasets

| S-EPMC5090204 | biostudies-literature
| S-EPMC8383285 | biostudies-literature
| S-EPMC4210135 | biostudies-literature
| S-EPMC9010562 | biostudies-literature
| S-EPMC7913509 | biostudies-literature
| S-EPMC96996 | biostudies-literature
| S-EPMC3406751 | biostudies-literature
| S-EPMC3072574 | biostudies-literature
| S-EPMC5673212 | biostudies-literature
| S-EPMC3317112 | biostudies-literature