Literature DB >> 19000763

Novel anti-infectives: is host defence the answer?

Pamela Hamill1, Kelly Brown, Håvard Jenssen, Robert E W Hancock.   

Abstract

Resistance to antimicrobial agents and the limited development of novel agents are threatening to worsen the burden of infections that are already a leading cause of morbidity and mortality. This has increased interest in the development of novel strategies such as selective modulation of our natural immune defences. Innate immunity is a complex, evolutionarily conserved, multi-facetted response to defeating infection that is naturally stimulated by pathogenic organisms through pattern recognition receptors on host cells. It is amplifiable and broad spectrum but if overstimulated can lead to the potential for harmful inflammatory responses. A broad variety of therapies are already available or increasingly under development, to stimulate protective innate immunity without overtly stimulating harmful inflammation or even suppressing such damaging pro-inflammatory responses.

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Year:  2008        PMID: 19000763     DOI: 10.1016/j.copbio.2008.10.006

Source DB:  PubMed          Journal:  Curr Opin Biotechnol        ISSN: 0958-1669            Impact factor:   9.740


  30 in total

Review 1.  Modulating immunity as a therapy for bacterial infections.

Authors:  Robert E W Hancock; Anastasia Nijnik; Dana J Philpott
Journal:  Nat Rev Microbiol       Date:  2012-03-16       Impact factor: 60.633

Review 2.  Cationic antimicrobial peptides in clinical development, with special focus on thanatin and heliomicin.

Authors:  E Andrès
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2011-10-01       Impact factor: 3.267

3.  Cathelicidin peptide LL-37 modulates TREM-1 expression and inflammatory responses to microbial compounds.

Authors:  Gimano D Amatngalim; Anastasia Nijnik; Pieter S Hiemstra; Robert E W Hancock
Journal:  Inflammation       Date:  2011-10       Impact factor: 4.092

4.  Modulation of the local neutrophil response by a novel hyaluronic acid-binding peptide reduces bacterial burden during staphylococcal wound infection.

Authors:  Jerry C Lee; Jennifer L Greenwich; George G Zhanel; Xiaobing Han; Andrew Cumming; Laura Saward; Rachel M McLoughlin
Journal:  Infect Immun       Date:  2010-07-19       Impact factor: 3.441

5.  A lack of synergy between membrane-permeabilizing cationic antimicrobial peptides and conventional antibiotics.

Authors:  Jing He; Charles G Starr; William C Wimley
Journal:  Biochim Biophys Acta       Date:  2014-09-28

Review 6.  Antimicrobial peptides: successes, challenges and unanswered questions.

Authors:  William C Wimley; Kalina Hristova
Journal:  J Membr Biol       Date:  2011-01-12       Impact factor: 1.843

7.  Progressive structuring of a branched antimicrobial peptide on the path to the inner membrane target.

Authors:  Yang Bai; Shouping Liu; Jianguo Li; Rajamani Lakshminarayanan; Padmanabhan Sarawathi; Charles Tang; Duncun Ho; Chandra Verma; Roger W Beuerman; Konstantin Pervushin
Journal:  J Biol Chem       Date:  2012-06-14       Impact factor: 5.157

8.  A small molecule deubiquitinase inhibitor increases localization of inducible nitric oxide synthase to the macrophage phagosome and enhances bacterial killing.

Authors:  Kristin M Burkholder; Jeffrey W Perry; Christiane E Wobus; Nicholas J Donato; Hollis D Showalter; Vaibhav Kapuria; Mary X D O'Riordan
Journal:  Infect Immun       Date:  2011-09-12       Impact factor: 3.441

9.  Properties of antibodies to a synthetic peptide representing an epitope shared by receptors of the type I cytokine family.

Authors:  Carlos G Belloc; Marisol Aguirre; Clara Peña; José L Aparicio; Maite Duhalde Vega; Sarah Dormois; Lilia A Retegui
Journal:  Clin Exp Med       Date:  2013-02       Impact factor: 3.984

Review 10.  Application of Synthetic Molecular Evolution to the Discovery of Antimicrobial Peptides.

Authors:  William C Wimley
Journal:  Adv Exp Med Biol       Date:  2019       Impact factor: 2.622

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