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Chitin Analog AVR-25 Prevents Experimental Bronchopulmonary Dysplasia.
Das, Pragnya; Acharya, Suchismita; Shah, Dilip; Agarwal, Beamon; Prahaladan, Varsha; Bhandari, Vineet.
Afiliación
  • Das P; Department of Pediatrics, Division of Neonatology, Drexel University, Philadelphia, Pennsylvania, United States.
  • Acharya S; Acceleration Laboratory, University of North Texas Health Science Center, Fort Worth, Texas, United States.
  • Shah D; AyuVis Research Inc, Fort Worth, Texas, United States.
  • Agarwal B; Department of Pediatrics, Division of Neonatology, Drexel University, Philadelphia, Pennsylvania, United States.
  • Prahaladan V; GenomeRxUS, Secane, Pennsylvania, United States.
  • Bhandari V; Department of Pediatrics, Division of Neonatology, Drexel University, Philadelphia, Pennsylvania, United States.
J Pediatr Intensive Care ; 9(3): 225-232, 2020 Sep.
Article en En | MEDLINE | ID: mdl-32685255
ABSTRACT
Infants born extremely preterm are at a high risk of developing bronchopulmonary dysplasia (BPD) which is characterized by large, simplified alveoli, increased inflammation, disrupted and dysregulated vasculogenesis, decreased cell proliferation, and increased cell death in the lungs. Due to lack of specific drug treatments to combat this condition, BPD and its long-term complications have taken a significant toll of healthcare resources. AVR-25, a novel immune modulator experimental compound, was able to partially recover the pulmonary phenotype in the hyperoxia-induced experimental mouse model of BPD. We anticipate that AVR-25 will have therapeutic potential for managing human BPD.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Pediatr Intensive Care Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Pediatr Intensive Care Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos