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Phage Therapy of Mycobacterium Infections: Compassionate Use of Phages in 20 Patients With Drug-Resistant Mycobacterial Disease.
Dedrick, Rebekah M; Smith, Bailey E; Cristinziano, Madison; Freeman, Krista G; Jacobs-Sera, Deborah; Belessis, Yvonne; Whitney Brown, A; Cohen, Keira A; Davidson, Rebecca M; van Duin, David; Gainey, Andrew; Garcia, Cristina Berastegui; Robert George, C R; Haidar, Ghady; Ip, Winnie; Iredell, Jonathan; Khatami, Ameneh; Little, Jessica S; Malmivaara, Kirsi; McMullan, Brendan J; Michalik, David E; Moscatelli, Andrea; Nick, Jerry A; Tupayachi Ortiz, Maria G; Polenakovik, Hari M; Robinson, Paul D; Skurnik, Mikael; Solomon, Daniel A; Soothill, James; Spencer, Helen; Wark, Peter; Worth, Austen; Schooley, Robert T; Benson, Constance A; Hatfull, Graham F.
Afiliação
  • Dedrick RM; Department of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Smith BE; Department of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Cristinziano M; Department of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Freeman KG; Department of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Jacobs-Sera D; Department of Biological Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Belessis Y; School of Women's and Children's Health, University of New South Wales, Sydney, New South Wales, Australia.
  • Whitney Brown A; Department of Respiratory Medicine, Sydney Children's Hospital, Sydney, New South Wales, Australia.
  • Cohen KA; Inova Fairfax Hospital, Falls Church, Virginia, USA.
  • Davidson RM; Division of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • van Duin D; Center for Genes, Environment, and Health, National Jewish Health, Denver, Colorado, USA.
  • Gainey A; Division of Infectious Diseases, University of North Carolina, Chapel Hill, North Carolina, USA.
  • Garcia CB; Department of Pharmacy, Division of Pediatric Infectious Diseases, Prisma Health Children's Hospital-Midlands, Columbia, South Carolina, USA.
  • Robert George CR; Department of Respiratory Disease, Hospital Universitari Vall d'Hebron, Barcelona, Spain.
  • Haidar G; New South Wales Health Pathology Microbiology, John Hunter Hospital, New Lambton, New South Wales, Australia.
  • Ip W; Department of Medicine, Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
  • Iredell J; Department of Pediatric Immunology, Great Ormond Street Hospital, London, United Kingdom.
  • Khatami A; Department of Immunology and Infectious Diseases, Sydney Children's Hospital, Randwick, New South Wales, Australia.
  • Little JS; Department of Infectious Diseases and Microbiology, Children's Hospital at Westmead, Westmead, New South Wales, Australia.
  • Malmivaara K; Discipline of Child and Adolescent Health, University of Syndey, Sydney, New South Wales, Australia.
  • McMullan BJ; Division of Infectious Diseases, Brigham and Women's Hospital, Boston, Massachusetts, USA.
  • Michalik DE; Great Ormond Street Hospital, London, United Kingdom.
  • Moscatelli A; Department of Immunology and Infectious Diseases, Sydney Children's Hospital, Randwick, New South Wales, Australia.
  • Nick JA; Miller Children's and Women's Hospital, Division of Pediatric Infectious Diseases, Long Beach, California, USA.
  • Tupayachi Ortiz MG; Neonatal and Pediatric Intensive Care Unit, Instituto Giannina Gaslini, Genoa, Italy.
  • Polenakovik HM; Department of Medicine, National Jewish Health, Denver, Colorado, USA.
  • Robinson PD; Department of Medicine, Division of Pulmonary and Critical Care Medicine, Miller School of Medicine, University of Miami, Miami, Florida, USA.
  • Skurnik M; Internal Medicine Department, Dayton Children's Hospital, Boonshoft School of Medicine, Wright State University, Dayton, Ohio, USA.
  • Solomon DA; Department of Respiratory Medicine, The Children's Hospital at Westmead, Westmead, New South Wales, Australia.
  • Soothill J; Department of Bacteriology and Immunology, Human Microbiome Research Program, University of Helsinki, Helsinki, Finland.
  • Spencer H; Division of Clinical Microbiology, Helsinki University Hospital, Helsinki, Finland.
  • Wark P; Division of Infectious Diseases, Brigham and Women's Hospital, Boston, Massachusetts, USA.
  • Worth A; Great Ormond Street Hospital, London, United Kingdom.
  • Schooley RT; Respiratory Medicine and Cardiothoracic Transplantation, Great Ormond Street Hospital, London, United Kingdom.
  • Benson CA; Immune Health Program, Hunter Medical Research Institute, University of Newcastle, Callaghan, New South Wales, Australia.
  • Hatfull GF; Department of Pediatric Immunology, Great Ormond Street Hospital, London, United Kingdom.
Clin Infect Dis ; 76(1): 103-112, 2023 01 06.
Article em En | MEDLINE | ID: mdl-35676823
ABSTRACT

BACKGROUND:

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.

METHODS:

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 compassionate use basis and patients were monitored for adverse reactions, clinical and microbiologic responses, the emergence of phage resistance, and phage neutralization in serum, sputum, or bronchoalveolar lavage fluid.

RESULTS:

No adverse reactions attributed to therapy were seen in any patient regardless of the pathogen, phages administered, or the route of delivery. Favorable clinical or microbiological responses were observed in 11 patients. Neutralizing antibodies were identified in serum after initiation of phage delivery intravenously in 8 patients, potentially contributing to lack of treatment response in 4 cases, but were not consistently associated with unfavorable responses in others. Eleven patients were treated with only a single phage, and no phage resistance was observed in any of these.

CONCLUSIONS:

Phage treatment of Mycobacterium infections is challenging due to the limited repertoire of therapeutically useful phages, but favorable clinical outcomes in patients lacking any other treatment options support continued development of adjunctive phage therapy for some mycobacterial infections.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bacteriófagos / Fibrose Cística / Terapia por Fagos / Mycobacterium / Infecções por Mycobacterium não Tuberculosas Limite: Humans Idioma: En Revista: Clin Infect Dis Assunto da revista: DOENCAS TRANSMISSIVEIS Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bacteriófagos / Fibrose Cística / Terapia por Fagos / Mycobacterium / Infecções por Mycobacterium não Tuberculosas Limite: Humans Idioma: En Revista: Clin Infect Dis Assunto da revista: DOENCAS TRANSMISSIVEIS Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos