TY - JOUR
T1 - The importance of lytic and nonlytic immune responses in viral infections
AU - Wodarz, Dominik
AU - Christensen, Jan Pravsgaard
AU - Thomsen, Allan Randrup
N1 - Keywords: Animals; Cytotoxicity, Immunologic; Genes, MHC Class I; Genes, MHC Class II; Humans; Lymphocytic choriomeningitis virus; Mice; Mice, Knockout; Models, Immunological; Models, Theoretical; T-Lymphocytes, Cytotoxic; Vesicular stomatitis Indiana virus; Virus Diseases; Virus Replication
PY - 2002
Y1 - 2002
N2 - Antiviral immune effector mechanisms can be divided broadly into lytic and nonlytic components. We use mathematical models to investigate the fundamental question of which type of response is required to combat different types of viral infection. According to our model, the relative roles of the two types of component depend on the cytopathicity of the virus relative to its rate of replication. If the viral cytopathicity is low relative to the rate of viral replication, the model predicts that a combination of lytic and nonlytic effector mechanisms is likely to be required to resolve the disease, particularly if the virus replicates at a fast rate. By contrast, if viral cytopathicity is high relative to the replication rate of the virus, then lytic and nonlytic mechanisms can, in principle, resolve the infection independently. We discuss our findings in the context of specific viral infections and use our model to interpret empirical data.
AB - Antiviral immune effector mechanisms can be divided broadly into lytic and nonlytic components. We use mathematical models to investigate the fundamental question of which type of response is required to combat different types of viral infection. According to our model, the relative roles of the two types of component depend on the cytopathicity of the virus relative to its rate of replication. If the viral cytopathicity is low relative to the rate of viral replication, the model predicts that a combination of lytic and nonlytic effector mechanisms is likely to be required to resolve the disease, particularly if the virus replicates at a fast rate. By contrast, if viral cytopathicity is high relative to the replication rate of the virus, then lytic and nonlytic mechanisms can, in principle, resolve the infection independently. We discuss our findings in the context of specific viral infections and use our model to interpret empirical data.
M3 - Journal article
C2 - 11923114
SN - 1471-4906
VL - 23
SP - 194
EP - 200
JO - Trends in Immunology
JF - Trends in Immunology
IS - 4
ER -