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The Lung Allograft Microbiome Associates with Pepsin, Inflammation, and Primary Graft Dysfunction.
McGinniss, John E; Whiteside, Samantha A; Deek, Rebecca A; Simon-Soro, Aurea; Graham-Wooten, Jevon; Oyster, Michelle; Brown, Melanie D; Cantu, Edward; Diamond, Joshua M; Li, Hongzhe; Christie, Jason D; Bushman, Frederic D; Collman, Ronald G.
Afiliación
  • McGinniss JE; Division of Pulmonary, Allergy, and Critical Care, Department of Medicine.
  • Whiteside SA; Division of Pulmonary, Allergy, and Critical Care, Department of Medicine.
  • Deek RA; Department of Epidemiology, Biostatistics, and Informatics.
  • Simon-Soro A; Division of Pulmonary, Allergy, and Critical Care, Department of Medicine.
  • Graham-Wooten J; Division of Pulmonary, Allergy, and Critical Care, Department of Medicine.
  • Oyster M; Division of Pulmonary, Allergy, and Critical Care, Department of Medicine.
  • Brown MD; Division of Pulmonary, Allergy, and Critical Care, Department of Medicine.
  • Cantu E; Department of Surgery, and.
  • Diamond JM; Division of Pulmonary, Allergy, and Critical Care, Department of Medicine.
  • Li H; Department of Epidemiology, Biostatistics, and Informatics.
  • Christie JD; Division of Pulmonary, Allergy, and Critical Care, Department of Medicine.
  • Bushman FD; Department of Microbiology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.
  • Collman RG; Division of Pulmonary, Allergy, and Critical Care, Department of Medicine.
Am J Respir Crit Care Med ; 206(12): 1508-1521, 2022 12 15.
Article en En | MEDLINE | ID: mdl-36103583
ABSTRACT
Rationale Primary graft dysfunction (PGD) is the principal cause of early morbidity and mortality after lung transplantation. The lung microbiome has been implicated in later transplantation outcomes but has not been investigated in PGD.

Objectives:

To define the peritransplant bacterial lung microbiome and relationship to host response and PGD.

Methods:

This was a single-center prospective cohort study. Airway lavage samples from donor lungs before organ procurement and recipient allografts immediately after implantation underwent bacterial 16S ribosomal ribonucleic acid gene sequencing. Recipient allograft samples were analyzed for cytokines by multiplex array and pepsin by ELISA. Measurements and Main

Results:

We enrolled 139 transplant subjects and obtained donor lung (n = 109) and recipient allograft (n = 136) samples. Severe PGD (persistent grade 3) developed in 15 subjects over the first 72 hours, and 40 remained without PGD (persistent grade 0). The microbiome of donor lungs differed from healthy lungs, and recipient allograft microbiomes differed from donor lungs. Development of severe PGD was associated with enrichment in the immediate postimplantation lung of oropharyngeal anaerobic taxa, particularly Prevotella. Elevated pepsin, a gastric biomarker, and a hyperinflammatory cytokine profile were present in recipient allografts in severe PGD and strongly correlated with microbiome composition. Together, immediate postimplantation allograft Prevotella/Streptococcus ratio, pepsin, and indicator cytokines were associated with development of severe PGD during the 72-hour post-transplantation period (area under the curve = 0.81).

Conclusions:

Lung allografts that develop PGD have a microbiome enriched in anaerobic oropharyngeal taxa, elevated gastric pepsin, and hyperinflammatory phenotype. These findings suggest a possible role for peritransplant aspiration in PGD, a potentially actionable mechanism that warrants further investigation.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trasplante de Pulmón / Disfunción Primaria del Injerto / Microbiota Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Am J Respir Crit Care Med Asunto de la revista: TERAPIA INTENSIVA Año: 2022 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trasplante de Pulmón / Disfunción Primaria del Injerto / Microbiota Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Am J Respir Crit Care Med Asunto de la revista: TERAPIA INTENSIVA Año: 2022 Tipo del documento: Article