A Retrospective, Observational Study of 12 Cases of Expanded-Access Customized Phage Therapy: Production, Characteristics, and Clinical Outcomes

Abstract Background Antimicrobial resistance (AMR) is undermining modern medicine, a problem compounded by bacterial adaptation to antibiotic pressures. Phages are viruses that infect bacteria. Their diversity and evolvability offer the prospect of their use as a therapeutic solution. Reported are o...

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Veröffentlicht in:Clinical infectious diseases 2023-10, Vol.77 (8), p.1079-1091
Hauptverfasser: Green, Sabrina I, Clark, Justin R, Santos, Haroldo H, Weesner, Kyle E, Salazar, Keiko C, Aslam, Saima, Campbell, J William, Doernberg, Sarah B, Blodget, Emily, Morris, Michele I, Suh, Gina A, Obeid, Karam, Silveira, Fernanda P, Filippov, Andrey A, Whiteson, Katrine L, Trautner, Barbara W, Terwilliger, Austen L, Maresso, Anthony
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Sprache:eng
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Zusammenfassung:Abstract Background Antimicrobial resistance (AMR) is undermining modern medicine, a problem compounded by bacterial adaptation to antibiotic pressures. Phages are viruses that infect bacteria. Their diversity and evolvability offer the prospect of their use as a therapeutic solution. Reported are outcomes of customized phage therapy for patients with difficult-to-treat antimicrobial resistant infections. Methods We retrospectively assessed 12 cases of customized phage therapy from a phage production center. Phages were screened, purified, sequenced, characterized, and Food and Drug Administration–approved via the IND (investigational new drug) compassionate-care route. Outcomes were assessed as favorable or unfavorable by microbiologic and clinical standards. Infections were device-related or systemic. Other experiences such as time to treatment, antibiotic synergy, and immune responses were recorded. Results Fifty requests for phage therapy were received. Customized phages were generated for 12 patients. After treatment, 42% (5/12) of cases showed bacterial eradication and 58% (7/12) showed clinical improvement, with two-thirds of all cases (66%) showing favorable responses. No major adverse reactions were observed. Antibiotic-phage synergy in vitro was observed in most cases. Immunological neutralization of phages was reported in 5 cases. Several cases were complicated by secondary infections. Complete characterization of the phages (morphology, genomics, and activity) and their production (methods, sterility, and endotoxin tests) are reported. Conclusions Customized phage production and therapy was safe and yielded favorable clinical or microbiological outcomes in two-thirds of cases. A center or pipeline dedicated to tailoring the phages against a patient's specific AMR bacterial infection may be a viable option where standard treatment has failed. Antimicrobial resistant infections present clinical challenges. Here, we report the experiences and outcomes of a dedicated phage discovery, manufacturing, and characterization platform for customized phage therapy for a range of heterogenous and complex resistant bacterial infections.
ISSN:1058-4838
1537-6591
DOI:10.1093/cid/ciad335