Literature DB >> 22971066

Current dilemmas in antimicrobial therapy in cystic fibrosis.

Kamini Jain1, Alan R Smyth.   

Abstract

The majority of cystic fibrosis (CF)-related morbidity and mortality is caused by pulmonary damage due to recurrent and chronic infections. Considerable improvements in the survival of individuals with CF have been achieved in recent decades, some of which may be due to better management of common pathogens such as Staphylococcus aureus and Pseudomonas aeruginosa. While the search continues for the optimal approach for prophylaxis, eradication and maintenance treatment of infections, there are several unanswered questions, posing dilemmas related to various therapeutic choices. Microbes pose additional challenges by adapting to CF lungs and developing treatment resistance. Several new, highly antimicrobial-resistant pathogens have emerged. Their pathogenic role in the progression of CF lung disease is not yet clear and effective treatment approaches have not been defined. There is an urgent need for well-designed comparative clinical trials of new antibiotic strategies.

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Year:  2012        PMID: 22971066     DOI: 10.1586/ers.12.39

Source DB:  PubMed          Journal:  Expert Rev Respir Med        ISSN: 1747-6348            Impact factor:   3.772


  8 in total

1.  Quorum sensing controls the Pseudomonas aeruginosa CRISPR-Cas adaptive immune system.

Authors:  Nina M Høyland-Kroghsbo; Jon Paczkowski; Sampriti Mukherjee; Jenny Broniewski; Edze Westra; Joseph Bondy-Denomy; Bonnie L Bassler
Journal:  Proc Natl Acad Sci U S A       Date:  2016-11-14       Impact factor: 11.205

2.  Type IV pilus glycosylation mediates resistance of Pseudomonas aeruginosa to opsonic activities of the pulmonary surfactant protein A.

Authors:  Rommel M Tan; Zhizhou Kuang; Yonghua Hao; Francis Lee; Timothy Lee; Ryan J Lee; Gee W Lau
Journal:  Infect Immun       Date:  2015-01-20       Impact factor: 3.441

3.  Potential of host defense peptide prodrugs as neutrophil elastase-dependent anti-infective agents for cystic fibrosis.

Authors:  Eanna Forde; Hilary Humphreys; Catherine M Greene; Deirdre Fitzgerald-Hughes; Marc Devocelle
Journal:  Antimicrob Agents Chemother       Date:  2013-11-25       Impact factor: 5.191

4.  Mitochondrial DAMPs induce endotoxin tolerance in human monocytes: an observation in patients with myocardial infarction.

Authors:  Irene Fernández-Ruiz; Francisco Arnalich; Carolina Cubillos-Zapata; Enrique Hernández-Jiménez; Raúl Moreno-González; Víctor Toledano; María Fernández-Velasco; Maria T Vallejo-Cremades; Laura Esteban-Burgos; Rebeca Pérez de Diego; Miguel A Llamas-Matias; Elena García-Arumi; Ramón Martí; Lisardo Boscá; Antoni L Andreu; José Luis López-Sendón; Eduardo López-Collazo
Journal:  PLoS One       Date:  2014-05-05       Impact factor: 3.240

Review 5.  Pseudomonas aeruginosa Diversification during Infection Development in Cystic Fibrosis Lungs-A Review.

Authors:  Ana Margarida Sousa; Maria Olívia Pereira
Journal:  Pathogens       Date:  2014-08-18

6.  In vitro and in vivo efficacy, toxicity, bio-distribution and resistance selection of a novel antibacterial drug candidate.

Authors:  Jlenia Brunetti; Chiara Falciani; Giulia Roscia; Simona Pollini; Stefano Bindi; Silvia Scali; Unai Cossio Arrieta; Vanessa Gómez-Vallejo; Leila Quercini; Elisa Ibba; Marco Prato; Gian Maria Rossolini; Jordi Llop; Luisa Bracci; Alessandro Pini
Journal:  Sci Rep       Date:  2016-05-12       Impact factor: 4.379

7.  Data Mining of Lung Microbiota in Cystic Fibrosis Patients.

Authors:  Jianguo Li; Chunyan Hao; Lili Ren; Yan Xiao; Jianwei Wang; Xuemei Qin
Journal:  PLoS One       Date:  2016-10-14       Impact factor: 3.240

Review 8.  Pathophysiology of endotoxin tolerance: mechanisms and clinical consequences.

Authors:  Eduardo López-Collazo; Carlos del Fresno
Journal:  Crit Care       Date:  2013-11-14       Impact factor: 9.097

  8 in total

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