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Published on: April 25, 2025
Potent antibody-mediated neutralization limits bacteriophage treatment of a pulmonary Mycobacterium abscessus
Rebekah M Dedrick1, Krista G Freeman1, Jan A Nguyen2
1Biological Sciences, University of Pittsburgh, Pittsburgh, PA, USA.
Abstract:
An 81-year-old immunocompetent patient with bronchiectasis and refractory Mycobacterium abscessus lung disease was treated for 6 months with a three-phage cocktail active against the strain. In this case study of phage to lower infectious burden, intravenous administration was safe and reduced the M. abscessus sputum load tenfold within one month. However, after two months, M. abscessus counts increased as the patient mounted a robust IgM- and IgG-mediated neutralizing antibody response to the phages, which was associated with limited therapeutic efficacy.
Insights
Bacteriophage therapy safely reduced Mycobacterium abscessus lung infections tenfold in an 81-year-old patient. However, the patient
Area of Science:
- Microbiology
- Immunology
- Pulmonary Medicine
Background:
- Bronchiectasis and refractory Mycobacterium abscessus lung disease present significant treatment challenges.
- Phage therapy is an emerging alternative for managing difficult-to-treat bacterial infections.
Observation:
- A case study involved an 81-year-old immunocompetent patient with bronchiectasis and refractory Mycobacterium abscessus lung disease.
- The patient received a three-phage cocktail administered intravenously for six months.
Findings:
- Intravenous phage administration was safe and reduced Mycobacterium abscessus sputum load by tenfold within one month.
- Therapeutic efficacy was limited after two months due to the development of a robust IgM- and IgG-mediated neutralizing antibody response to the phages.
Implications:
- This case highlights the potential of phage therapy in treating Mycobacterium abscessus lung disease.
- The development of neutralizing antibodies against bacteriophages can limit their long-term therapeutic efficacy.
- Further research is needed to overcome antibody-mediated resistance in phage therapy.
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