Assistant Professor of Anaesthesia (Pediatrics), Boston Children's Hospital

Pediatrics

Gregory Priebe works in the field of Pediatrics. He went to Harvard Medical School. Harvard Medical School is a one of the best medicals schools. Harvard Medical School is ranked 1/12 in Research/PrimaryCare. He has 1 awards "Fellow (FAAP)". Gregory Priebe is also a published doctor. He has 27 paper published. The most recent paper is: Strategies to prevent ventilator-associated pneumonia in acute care hospitals: 2014 update.

Publications

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• Strategies to prevent ventilator-associated pneumonia in acute care hospitals: 2014 update.
• Microbiota-driven immune cellular maturation is essential for antibody-mediated adaptive immunity to Staphylococcus aureus infection in the eye.
• Vaccines for Pseudomonas aeruginosa: a long and winding road.
• Genetic variation of a bacterial pathogen within individuals with cystic fibrosis provides a record of selective pressures.
• Trehalose Biosynthesis Promotes Pseudomonas aeruginosa Pathogenicity in Plants.
• Collaboration between macrophages and vaccine-induced CD4+ T cells confers protection against lethal Pseudomonas aeruginosa pneumonia during neutropenia.
• Hepoxilin a3 facilitates neutrophilic breach of lipoxygenase-expressing airway epithelial barriers.
• Th17-stimulating Protein Vaccines confer Protection against Pseudomonas aeruginosa Pneumonia.
• Targeting Pan-Resistant Bacteria With Antibodies to a Broadly Conserved Surface Polysaccharide Expressed During Infection.
• Parallel bacterial evolution within multiple patients identifies candidate pathogenicity genes.
• Mucosal vaccination with a multivalent, live-attenuated vaccine induces multifactorial immunity against Pseudomonas aeruginosa acute lung infection.
• Caveolin-1 modifies the immunity to Pseudomonas aeruginosa.
• Analysis of acquisition of Pseudomonas aeruginosa gastrointestinal mucosal colonization and horizontal transmission in a murine model.
• Inescapable need for neutrophils as mediators of cellular innate immunity to acute Pseudomonas aeruginosa pneumonia.
• IL-17 is a critical component of vaccine-induced protection against lung infection by lipopolysaccharide-heterologous strains of Pseudomonas aeruginosa.
• The neutrophil serine protease inhibitor serpinb1 preserves lung defense functions in Pseudomonas aeruginosa infection.
• A live-attenuated Pseudomonas aeruginosa vaccine elicits outer membrane protein-specific active and passive protection against corneal infection.
• Sepsis in the immunocompromised child: the least studied with the most to gain.
• Virulence of Pseudomonas aeruginosa in a murine model of gastrointestinal colonization and dissemination in neutropenia.
• Human monoclonal antibodies to Pseudomonas aeruginosa alginate that protect against infection by both mucoid and nonmucoid strains.
• The galU Gene of Pseudomonas aeruginosa is required for corneal infection and efficient systemic spread following pneumonia but not for infection confined to the lung.
• Protection against fatal Pseudomonas aeruginosa pneumonia in mice after nasal immunization with a live, attenuated aroA deletion mutant.
• Construction and characterization of a live, attenuated aroA deletion mutant of Pseudomonas aeruginosa as a candidate intranasal vaccine.
• High-frequency oscillatory ventilation in pediatric patients.
• Bacterial subretinal abscess: a case report and review of the literature.
• Acquisition of expression of the Pseudomonas aeruginosa ExoU cytotoxin leads to increased bacterial virulence in a murine model of acute pneumonia and systemic spread.

Schools

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• Harvard Medical School

• Children39s Hospital Boston

Doctors Specialties

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• Pediatric Critical Care Medicine
• Pediatric Infectious Disease Medicine
• Pediatrics

Accepted Insurances

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Awards

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• Fellow (FAAP)

Education

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• Boston Children's Hospital
• Harvard Medical School

Hospital

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• Boston Children's Hospital

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