<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Dedrick RM</submitter><funding>Jane and Aatos Erkko Foundation</funding><funding>Howard Hughes Medical Institute</funding><funding>Cystic Fibrosis Foundation</funding><funding>Burroughs Wellcome Fund</funding><funding>NIAID NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>National Heart, Lung, and Blood Institute</funding><funding>NIH</funding><funding>NIGMS NIH HHS</funding><pagination>103-112</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9825826</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>76(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Nontuberculous Mycobacterium infections, particularly Mycobacterium abscessus, are increasingly common among patients with cystic fibrosis and chronic bronchiectatic lung diseases. Treatment is challenging due to intrinsic antibiotic resistance. Bacteriophage therapy represents a potentially novel approach. Relatively few active lytic phages are available and there is great variation in phage susceptibilities among M. abscessus isolates, requiring personalized phage identification.&lt;h4>Methods&lt;/h4>Mycobacterium isolates from 200 culture-positive patients with symptomatic disease were screened for phage susceptibilities. One or more lytic phages were identified for 55 isolates. Phages were administered intravenously, by aerosolization, or both to 20 patients on a compassio</pubmed_abstract><journal>Clinical infectious diseases : an official publication of the Infectious Diseases Society of America</journal><pubmed_title>Phage Therapy of Mycobacterium Infections: Compassionate Use of Phages in 20 Patients With Drug-Resistant Mycobacterial Disease.</pubmed_title><pmcid>PMC9825826</pmcid><funding_grant_id>NICK20Y2-SVC and NICK20Y2-OUT</funding_grant_id><funding_grant_id>HATFUL19GO</funding_grant_id><funding_grant_id>GM131729</funding_grant_id><funding_grant_id>HL146228</funding_grant_id><funding_grant_id>NICK20Y2-OUT</funding_grant_id><funding_grant_id>R35 GM131729</funding_grant_id><funding_grant_id>K08 HL139994</funding_grant_id><funding_grant_id>R01 HL090991</funding_grant_id><funding_grant_id>R01 HL146228</funding_grant_id><funding_grant_id>K08 HL139994-01</funding_grant_id><funding_grant_id>NICK20Y2-SVC</funding_grant_id><funding_grant_id>K23 AI154546</funding_grant_id><funding_grant_id>AI154546</funding_grant_id><funding_grant_id>GT12053</funding_grant_id><funding_grant_id>R01HL146228</funding_grant_id><pubmed_authors>Little JS</pubmed_authors><pubmed_authors>Nick JA</pubmed_authors><pubmed_authors>Whitney Brown A</pubmed_authors><pubmed_authors>Skurnik M</pubmed_authors><pubmed_authors>Cristinziano M</pubmed_authors><pubmed_authors>Solomon DA</pubmed_authors><pubmed_authors>Khatami A</pubmed_authors><pubmed_authors>Hatfull GF</pubmed_authors><pubmed_authors>Wark P</pubmed_authors><pubmed_authors>Robert George CR</pubmed_authors><pubmed_authors>Dedrick RM</pubmed_authors><pubmed_authors>Belessis Y</pubmed_authors><pubmed_authors>Ip W</pubmed_authors><pubmed_authors>Malmivaara K</pubmed_authors><pubmed_authors>Haidar G</pubmed_authors><pubmed_authors>Iredell J</pubmed_authors><pubmed_authors>Tupayachi Ortiz MG</pubmed_authors><pubmed_authors>Benson CA</pubmed_authors><pubmed_authors>Moscatelli A</pubmed_authors><pubmed_authors>Smith BE</pubmed_authors><pubmed_authors>Davidson RM</pubmed_authors><pubmed_authors>Michalik DE</pubmed_authors><pubmed_authors>Freeman KG</pubmed_authors><pubmed_authors>van Duin D</pubmed_authors><pubmed_authors>Garcia CB</pubmed_authors><pubmed_authors>Worth A</pubmed_authors><pubmed_authors>Robinson PD</pubmed_authors><pubmed_authors>Cohen KA</pubmed_authors><pubmed_authors>Gainey A</pubmed_authors><pubmed_authors>Jacobs-Sera D</pubmed_authors><pubmed_authors>Soothill J</pubmed_authors><pubmed_authors>Polenakovik HM</pubmed_authors><pubmed_authors>Spencer H</pubmed_authors><pubmed_authors>McMullan BJ</pubmed_authors><pubmed_authors>Schooley RT</pubmed_authors></additional><is_claimable>false</is_claimable><name>Phage Therapy of Mycobacterium Infections: Compassionate Use of Phages in 20 Patients With Drug-Resistant Mycobacterial Disease.</name><description>&lt;h4>Background&lt;/h4>Nontuberculous Mycobacterium infections, particularly Mycobacterium abscessus, are increasingly common among patients with cystic fibrosis and chronic bronchiectatic lung diseases. Treatment is challenging due to intrinsic antibiotic resistance. Bacteriophage therapy represents a potentially novel approach. Relatively few active lytic phages are available and there is great variation in phage susceptibilities among M. abscessus isolates, requiring personalized phage identification.&lt;h4>Methods&lt;/h4>Mycobacterium isolates from 200 culture-positive patients with symptomatic disease were screened for phage susceptibilities. One or more lytic phages were identified for 55 isolates. Phages were administered intravenously, by aerosolization, or both to 20 patients on a compassio</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2026-04-08T16:08:39.045Z</modification><creation>2025-04-06T11:43:28.136Z</creation></dates><accession>S-EPMC9825826</accession><cross_references><pubmed>35676823</pubmed><doi>10.1093/cid/ciac453</doi></cross_references></HashMap>