坏死性小肠结肠炎
医学
疾病
动物模型
转化研究
重症监护医学
先天免疫系统
混乱
生物信息学
免疫系统
免疫学
生物
病理
儿科
内分泌学
心理学
精神分析
作者
Carla M. Lopez,Maame Efua Sampah,Johannes W. Duess,Asuka Ishiyama,Raheel Ahmad,Chhinder P. Sodhi,David J. Hackam
标识
DOI:10.1016/j.semperi.2022.151695
摘要
Necrotizing enterocolitis (NEC) is the leading cause of death and disability from gastrointestinal disease in premature infants. The mortality of patients with NEC is approximately 30%, a figure that has not changed in many decades, reflecting the need for a greater understanding of its pathogenesis. Progress towards understanding the cellular and molecular mechanisms underlying NEC requires the study of highly translational animal models. Such animal models must mimic the biology and physiology of premature infants, while still allowing for safe experimental manipulation of environmental and microbial factors thought to be associated with the risk and severity of NEC. Findings from animal models have yielded insights into the interactions between the host, the colonizing microbes, and the innate immune receptor Toll-like Receptor 4 (TLR4) in driving disease development. This review discusses the relative strengths and weaknesses of available in vivo, in vitro, and NEC-in-a-dish models of this disease. We also highlight the unique contributions that each model has made to our understanding of the complex interactions between enterocytes, microbiota, and immune cells in the pathogenesis of NEC. The overall purpose of this review is to provide a menu of options regarding currently available animal models of NEC, while in parallel hopefully reducing the potential uncertainty and confusion regarding NEC models to assist those who wish to enter this field from other disciplines.
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