TY - JOUR
T1 - Model Systems
T2 - Transgenic mouse models for measles pathogenesis
AU - Manchester, Marianne
AU - Rall, Glenn R.
PY - 2001/1/1
Y1 - 2001/1/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=0035012262&partnerID=8YFLogxK
U2 - 10.1016/S0966-842X(00)01903-X
DO - 10.1016/S0966-842X(00)01903-X
M3 - Review article
SN - 0966-842X
VL - 9
SP - 19
EP - 23
JO - Trends in Microbiology
JF - Trends in Microbiology
IS - 1
ER -