Literature DB >> 27015977

A novel approach for emerging and antibiotic resistant infections: Innate defense regulators as an agnostic therapy.

John R North1, Shunsuke Takenaka1, Annett Rozek1, Agnieszka Kielczewska1, Steven Opal2, Lisa A Morici3, B Brett Finlay4, Christopher J Schaber5, Richard Straube5, Oreola Donini6.   

Abstract

Innate Defense Regulators (IDRs) are short synthetic peptides that target the host innate immune system via an intracellular adaptor protein which functions at key signaling nodes. In this work, further details of the mechanism of action of IDRs have been discovered. The studies reported here show that the lead clinical IDR, SGX94, has broad-spectrum activity against Gram-negative and Gram-positive bacterial infections caused by intracellular or extracellular bacteria and also complements the actions of standard of care antibiotics. Based on in vivo and primary cell culture studies, this activity is shown to result from the primary action of SGX94 on tissue-resident cells and subsequent secondary signaling to activate myeloid-derived cells, resulting in enhanced bacterial clearance and increased survival. Data from non-clinical and clinical studies also show that SGX94 treatment modulates pro-inflammatory and anti-inflammatory cytokine levels, thereby mitigating the deleterious inflammatory consequences of innate immune activation. Since they act through host pathways to provide both broad-spectrum anti-infective capability as well as control of inflammation, IDRs are unlikely to be impacted by resistance mechanisms and offer potential clinical advantages in the fight against emerging and antibiotic resistant bacterial infections.
Copyright © 2016 The Authors. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Anti-infective; Anti-inflammatory; Antibacterial; Broad spectrum; Cefepime (PubChem CID: 9571075); Doxycycline (PubChem CID: 54671203); Dusquetide (PubChem CID: 71722017); Immune; Innate; Vancomycin (PubChem CID: 14969)

Mesh:

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Year:  2016        PMID: 27015977      PMCID: PMC4867239          DOI: 10.1016/j.jbiotec.2016.03.032

Source DB:  PubMed          Journal:  J Biotechnol        ISSN: 0168-1656            Impact factor:   3.307


  35 in total

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5.  Regulation of MyD88 aggregation and the MyD88-dependent signaling pathway by sequestosome 1 and histone deacetylase 6.

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Journal:  J Biol Chem       Date:  2010-09-13       Impact factor: 5.157

6.  Tumour necrosis factor alpha and its soluble receptors in juvenile chronic arthritis.

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Review 7.  New thoughts on the initiation of mucositis.

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8.  Human IL-23-producing type 1 macrophages promote but IL-10-producing type 2 macrophages subvert immunity to (myco)bacteria.

Authors:  Frank A W Verreck; Tjitske de Boer; Dennis M L Langenberg; Marieke A Hoeve; Matthijs Kramer; Elena Vaisberg; Robert Kastelein; Arend Kolk; René de Waal-Malefyt; Tom H M Ottenhoff
Journal:  Proc Natl Acad Sci U S A       Date:  2004-03-19       Impact factor: 11.205

9.  The sequestosome 1/p62 attenuates cytokine gene expression in activated macrophages by inhibiting IFN regulatory factor 8 and TNF receptor-associated factor 6/NF-kappaB activity.

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  6 in total

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2.  Dusquetide modulates innate immune response through binding to p62.

Authors:  Yi Zhang; Christina G Towers; Upendra K Singh; Jiuyang Liu; Maria Håkansson; Derek T Logan; Oreola Donini; Tatiana G Kutateladze
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3.  Dusquetide: Reduction in oral mucositis associated with enduring ancillary benefits in tumor resolution and decreased mortality in head and neck cancer patients.

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Review 4.  Perspectives for clinical use of engineered human host defense antimicrobial peptides.

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Journal:  FEMS Microbiol Rev       Date:  2017-05-01       Impact factor: 16.408

Review 5.  Membrane Active Antimicrobial Peptides: Translating Mechanistic Insights to Design.

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Review 6.  How to Combat Gram-Negative Bacteria Using Antimicrobial Peptides: A Challenge or an Unattainable Goal?

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  6 in total

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