TY - JOUR
T1 - Antiviral response in pandemic influenza viruses
AU - García-Sastre, Adolfo
PY - 2006/1
Y1 - 2006/1
N2 - The outcome of viral infections depends on a complex set of interactions between the viruses and their hosts. Particularly, viral infection triggers specific signaling programs within the infected cells that results in substantial changes in host gene expression. While some of these changes might be beneficial for viral replication, others represent the induction of a host antiviral response. In this respect, viruses have evolved genes that counteract this initial innate antiviral response. These viral-host interactions shape the subsequent phases of the disease and influence the adaptive immune response. In influenza viruses, the nonstructural protein 1 inhibits the interferonmediated antiviral response. The regulatory activities of this viral protein play a major role in the pathogenicity of influenza virus and appear partially responsible for the ability of influenza viruses to infect multiple animal species, which likely contributes to the generation of new pandemic viruses in humans.
AB - The outcome of viral infections depends on a complex set of interactions between the viruses and their hosts. Particularly, viral infection triggers specific signaling programs within the infected cells that results in substantial changes in host gene expression. While some of these changes might be beneficial for viral replication, others represent the induction of a host antiviral response. In this respect, viruses have evolved genes that counteract this initial innate antiviral response. These viral-host interactions shape the subsequent phases of the disease and influence the adaptive immune response. In influenza viruses, the nonstructural protein 1 inhibits the interferonmediated antiviral response. The regulatory activities of this viral protein play a major role in the pathogenicity of influenza virus and appear partially responsible for the ability of influenza viruses to infect multiple animal species, which likely contributes to the generation of new pandemic viruses in humans.
UR - http://www.scopus.com/inward/record.url?scp=31344438094&partnerID=8YFLogxK
U2 - 10.3201/eid1201.051186
DO - 10.3201/eid1201.051186
M3 - Review article
C2 - 16494716
AN - SCOPUS:31344438094
SN - 1080-6040
VL - 12
SP - 44
EP - 47
JO - Emerging Infectious Diseases
JF - Emerging Infectious Diseases
IS - 1
ER -