Manchester M, Rall G F
Dept of Neuropharmacology (IMM6), The Scripps Research Institute, La Jolla, CA 92037, USA.
Trends Microbiol. 2001 Jan;9(1):19-23. doi: 10.1016/s0966-842x(00)01903-x.
Studies of the diseases caused by measles virus (MV) in humans have been restricted owing to the lack of suitable animal models. The discovery of cellular receptors for MV entry has facilitated the development of transgenic mice that are susceptible to MV infection, and that mimic certain aspects of the central nervous system diseases and immunosuppression that can occur in infected humans. Moreover, such mouse models have allowed a clearer understanding of the contributions of the innate and adaptive immune response following infection, and will no doubt be important tools in the future for the development of new antiviral and vaccine reagents.
由于缺乏合适的动物模型,对人类麻疹病毒(MV)所致疾病的研究受到了限制。MV进入细胞的受体的发现推动了对MV感染易感的转基因小鼠的开发,这些小鼠可模拟受感染人类可能出现的某些中枢神经系统疾病和免疫抑制情况。此外,此类小鼠模型有助于更清楚地了解感染后固有免疫和适应性免疫反应所起的作用,并且无疑将成为未来开发新型抗病毒和疫苗试剂的重要工具。