Das Pragnya, Acharya Suchismita, Shah Dilip, Agarwal Beamon, Prahaladan Varsha, Bhandari Vineet
Department of Pediatrics, Division of Neonatology, Drexel University, Philadelphia, Pennsylvania, United States.
Acceleration Laboratory, University of North Texas Health Science Center, Fort Worth, Texas, United States.
J Pediatr Intensive Care. 2020 Sep;9(3):225-232. doi: 10.1055/s-0040-1709994. Epub 2020 May 8.
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.
极早产儿患支气管肺发育不良(BPD)的风险很高,其特征是肺泡大且结构简单、炎症增加、血管生成紊乱和失调、细胞增殖减少以及肺部细胞死亡增加。由于缺乏对抗这种疾病的特定药物治疗,BPD及其长期并发症消耗了大量医疗资源。新型免疫调节剂实验化合物AVR-25能够在高氧诱导的BPD实验小鼠模型中部分恢复肺表型。我们预计AVR-25在治疗人类BPD方面具有潜在的治疗价值。