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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/2451
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dc.contributor.authorDubey, Uma S.-
dc.contributor.authorDubey, Balram-
dc.date.accessioned2021-10-02T17:51:17Z-
dc.date.available2021-10-02T17:51:17Z-
dc.date.issued2021-
dc.identifier.urihttps://www.journals.vu.lt/nonlinear-analysis/article/view/21434-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2451-
dc.description.abstractVirus dynamics models are useful in interpreting and predicting the change in viral load over the time and the effect of treatment in emerging viral infections like HIV/AIDS, hepatitis B virus (HBV). We propose a mathematical model involving the role of total immune response (innate, CTL, and humoral) and treatment for productively infected cells and free virus to understand the dynamics of virus–host interactions. A threshold condition for the extinction or persistence of infection, i.e. basic reproductive number, in the presence of immune response (RI) is established. We study the global stability of virus-free equilibrium and interior equilibrium using LaSalle’s principle and Lyapunov’s direct method. The global stability of virus-free equilibrium ensures the clearance of virus from the body, which is independent of initial status of subpopulations. Central manifold theory is used to study the behavior of equilibrium pointsen_US
dc.language.isoenen_US
dc.publisherVUPen_US
dc.subjectBiologyen_US
dc.subjectVirus dynamics modelen_US
dc.subjectHumoral immune responseen_US
dc.subjectCTL-mediated immune responseen_US
dc.titleModeling the dynamics of viral–host interaction during treatment of productively infected cells and free virus involving total immune responseen_US
dc.typeArticleen_US
Appears in Collections:Department of Biological Sciences

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