Véronique Dartois , Tracey L. Bonfield , Jim P. Boyce , Charles L. Daley , Thomas Dick , Mercedes Gonzalez-Juarrero , Shashank Gupta , Igor Kramnik , Gyanu Lamichhane , Barbara E. Laughon , Nicola I. Lorè , Kenneth C. Malcolm , Kenneth N. Olivier , Katherine L. Tuggle , Mary Jackson
{"title":"用于测试抗脓肿分枝杆菌肺部感染的抗菌药物的临床前鼠模型:现行做法和建议","authors":"Véronique Dartois , Tracey L. Bonfield , Jim P. Boyce , Charles L. Daley , Thomas Dick , Mercedes Gonzalez-Juarrero , Shashank Gupta , Igor Kramnik , Gyanu Lamichhane , Barbara E. Laughon , Nicola I. Lorè , Kenneth C. Malcolm , Kenneth N. Olivier , Katherine L. Tuggle , Mary Jackson","doi":"10.1016/j.tube.2024.102503","DOIUrl":null,"url":null,"abstract":"<div><p><em>Mycobacterium abscessus</em>, a rapidly growing nontuberculous mycobacterium, is increasingly recognized as an important pathogen of the human lung, disproportionally affecting people with cystic fibrosis (CF) and other susceptible individuals with non-CF bronchiectasis and compromised immune functions. <em>M. abscessus</em> infections are extremely difficult to treat due to intrinsic resistance to many antibiotics, including most anti-tuberculous drugs. Current standard-of-care chemotherapy is long, includes multiple oral and parenteral repurposed drugs, and is associated with significant toxicity. The development of more effective oral antibiotics to treat <em>M. abscessus</em> infections has thus emerged as a high priority. While murine models have proven instrumental in predicting the efficacy of therapeutic treatments for <em>M. tuberculosis</em> infections, the preclinical evaluation of drugs against <em>M. abscessus</em> infections has proven more challenging due to the difficulty of establishing a progressive, sustained, pulmonary infection with this pathogen in mice. To address this issue, a series of three workshops were hosted in 2023 by the Cystic Fibrosis Foundation (CFF) and the National Institute of Allergy and Infectious Diseases (NIAID) to review the current murine models of <em>M. abscessus</em> infections, discuss current challenges and identify priorities toward establishing validated and globally harmonized preclinical models. This paper summarizes the key points from these workshops. The hope is that the recommendations that emerged from this exercise will facilitate the implementation of informative murine models of therapeutic efficacy testing across laboratories, improve reproducibility from lab-to-lab and accelerate preclinical-to-clinical translation.</p></div>","PeriodicalId":23383,"journal":{"name":"Tuberculosis","volume":"147 ","pages":"Article 102503"},"PeriodicalIF":2.8000,"publicationDate":"2024-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Preclinical murine models for the testing of antimicrobials against Mycobacterium abscessus pulmonary infections: Current practices and recommendations\",\"authors\":\"Véronique Dartois , Tracey L. Bonfield , Jim P. Boyce , Charles L. Daley , Thomas Dick , Mercedes Gonzalez-Juarrero , Shashank Gupta , Igor Kramnik , Gyanu Lamichhane , Barbara E. Laughon , Nicola I. Lorè , Kenneth C. Malcolm , Kenneth N. Olivier , Katherine L. Tuggle , Mary Jackson\",\"doi\":\"10.1016/j.tube.2024.102503\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><em>Mycobacterium abscessus</em>, a rapidly growing nontuberculous mycobacterium, is increasingly recognized as an important pathogen of the human lung, disproportionally affecting people with cystic fibrosis (CF) and other susceptible individuals with non-CF bronchiectasis and compromised immune functions. <em>M. abscessus</em> infections are extremely difficult to treat due to intrinsic resistance to many antibiotics, including most anti-tuberculous drugs. Current standard-of-care chemotherapy is long, includes multiple oral and parenteral repurposed drugs, and is associated with significant toxicity. The development of more effective oral antibiotics to treat <em>M. abscessus</em> infections has thus emerged as a high priority. While murine models have proven instrumental in predicting the efficacy of therapeutic treatments for <em>M. tuberculosis</em> infections, the preclinical evaluation of drugs against <em>M. abscessus</em> infections has proven more challenging due to the difficulty of establishing a progressive, sustained, pulmonary infection with this pathogen in mice. To address this issue, a series of three workshops were hosted in 2023 by the Cystic Fibrosis Foundation (CFF) and the National Institute of Allergy and Infectious Diseases (NIAID) to review the current murine models of <em>M. abscessus</em> infections, discuss current challenges and identify priorities toward establishing validated and globally harmonized preclinical models. This paper summarizes the key points from these workshops. 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Preclinical murine models for the testing of antimicrobials against Mycobacterium abscessus pulmonary infections: Current practices and recommendations
Mycobacterium abscessus, a rapidly growing nontuberculous mycobacterium, is increasingly recognized as an important pathogen of the human lung, disproportionally affecting people with cystic fibrosis (CF) and other susceptible individuals with non-CF bronchiectasis and compromised immune functions. M. abscessus infections are extremely difficult to treat due to intrinsic resistance to many antibiotics, including most anti-tuberculous drugs. Current standard-of-care chemotherapy is long, includes multiple oral and parenteral repurposed drugs, and is associated with significant toxicity. The development of more effective oral antibiotics to treat M. abscessus infections has thus emerged as a high priority. While murine models have proven instrumental in predicting the efficacy of therapeutic treatments for M. tuberculosis infections, the preclinical evaluation of drugs against M. abscessus infections has proven more challenging due to the difficulty of establishing a progressive, sustained, pulmonary infection with this pathogen in mice. To address this issue, a series of three workshops were hosted in 2023 by the Cystic Fibrosis Foundation (CFF) and the National Institute of Allergy and Infectious Diseases (NIAID) to review the current murine models of M. abscessus infections, discuss current challenges and identify priorities toward establishing validated and globally harmonized preclinical models. This paper summarizes the key points from these workshops. The hope is that the recommendations that emerged from this exercise will facilitate the implementation of informative murine models of therapeutic efficacy testing across laboratories, improve reproducibility from lab-to-lab and accelerate preclinical-to-clinical translation.
期刊介绍:
Tuberculosis is a speciality journal focusing on basic experimental research on tuberculosis, notably on bacteriological, immunological and pathogenesis aspects of the disease. The journal publishes original research and reviews on the host response and immunology of tuberculosis and the molecular biology, genetics and physiology of the organism, however discourages submissions with a meta-analytical focus (for example, articles based on searches of published articles in public electronic databases, especially where there is lack of evidence of the personal involvement of authors in the generation of such material). We do not publish Clinical Case-Studies.
Areas on which submissions are welcomed include:
-Clinical TrialsDiagnostics-
Antimicrobial resistance-
Immunology-
Leprosy-
Microbiology, including microbial physiology-
Molecular epidemiology-
Non-tuberculous Mycobacteria-
Pathogenesis-
Pathology-
Vaccine development.
This Journal does not accept case-reports.
The resurgence of interest in tuberculosis has accelerated the pace of relevant research and Tuberculosis has grown with it, as the only journal dedicated to experimental biomedical research in tuberculosis.