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Modelling intracellular delay and therapy interruptions within Ghanaian HIV population

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dc.contributor.author Owusu, Kofi F
dc.contributor.author Doungmo Goufo, Emile F
dc.contributor.author Mugisha, Stella
dc.date.accessioned 2020-09-01T03:51:22Z
dc.date.available 2020-09-01T03:51:22Z
dc.date.issued 2020-08-05
dc.identifier.citation Advances in Difference Equations. 2020 Aug 05;2020(1):401
dc.identifier.uri https://doi.org/10.1186/s13662-020-02856-x
dc.identifier.uri http://hdl.handle.net/10500/26631
dc.description.abstract Abstract This paper seeks to unveil the niche of delay differential equation in harmonizing low HIV viral haul and thereby articulating the adopted model, to delve into structured treatment interruptions. Therefore, an ordinary differential equation is schemed to consist of three components such as untainted CD4+ T-cells, tainted CD4+ T-cells (HIV) and CTL. A discrete time delay is ushered to the formulated model in order to account for vital components, such as intracellular delay and HIV latency which were missing in previous works but have been advocated for future research. It was divested that when the reproductive number was less than unity, the disease free equilibrium of the model was asymptotically stable. Hence the adopted model with or without the delay component articulates less production of virions as per the decline rate. Therefore CD4+ T-cells in the blood remains constant at δ 1 / δ 3 $\delta _{1} / \delta _{3}$ , hence declining the virions level in the blood. As per the adopted model, the best STI practice is intimated for compliance.
dc.title Modelling intracellular delay and therapy interruptions within Ghanaian HIV population
dc.type Journal Article
dc.date.updated 2020-09-01T03:51:22Z
dc.language.rfc3066 en
dc.rights.holder The Author(s)


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