- Series
- Mathematical Biology Seminar
- Time
- Wednesday, January 22, 2014 - 11:05am for 1 hour (actually 50 minutes)
- Location
- Skiles Bld Room 005
- Speaker
- Pavel Skums – CDC
- Organizer
- Leonid Bunimovich
Understanding the mechanisms responsible for the establishment of
chronic viral infections is critical to the development of efficient
therapeutics and vaccines against highly mutable RNA viruses, such as
Hepatitis C (HCV). The mechanism of intra-host viral evolution assumed
by most models is based on immune escape via random mutations. However,
continuous immune escape does not explain the recent observations of a
consistent increase in negative selection during chronic infection and
long-term persistence of individual viral variants, which suggests
extensive intra-host viral adaptation.
This talk explores the role of immune cross-reactivity of viral variants
in the establishment of chronic infection and viral intra-host
adaptation. Using a computational prediction model for
cross-immunoreactivity of viral variants, we show that the level of HCV
intra-host adaptation correlates with the rate of cross-immunoreactivity
among HCV quasispecies. We analyzed cross-reactivity networks (CRNs)
for HCV intra-host variants and found that the structure of CRNs
correlates with the type and strength of selection in viral populations.
Based on those observations, we developed a mathematical model
describing the immunological interaction among RNA viral variants that
involves, in addition to neutralization, a non-neutralizing
cross-immunoreactivity. The model describes how viral variants escape
immune responses and persist, owing to their capability to stimulate
non-neutralizing immune responses developed earlier against preceding
variants. The model predicts the mechanism of antigenic cooperation
among viral variants, which is based on the structure of CRNs. In
addition, the model allows to explain previously observed and
unexplained phenomenon of reappearance of viral variants: for some
chronically infected patients the variants sampled during the acute
stage are phylogenetically distant from variants sampled at the earlier
years of infection and intermixed with variants sampled 10-20 years
later.
(Joint work with Y. Khudyakov, Z.Dimitrova, D.Campo and L.Bunimovich)