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Modelling the Evolution and Spread of HIV Immune Escape Mutants

During infection with human immunodeficiency virus (HIV), immune pressure from cytotoxic T-lymphocytes (CTLs) selects for viral mutants that confer escape from CTL recognition. These escape variants can be transmitted between individuals where, depending upon their cost to viral fitness and the CTL...

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Autores principales: Fryer, Helen R., Frater, John, Duda, Anna, Roberts, Mick G., Phillips, Rodney E., McLean, Angela R.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2987822/
https://www.ncbi.nlm.nih.gov/pubmed/21124991
http://dx.doi.org/10.1371/journal.ppat.1001196
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author Fryer, Helen R.
Frater, John
Duda, Anna
Roberts, Mick G.
Phillips, Rodney E.
McLean, Angela R.
author_facet Fryer, Helen R.
Frater, John
Duda, Anna
Roberts, Mick G.
Phillips, Rodney E.
McLean, Angela R.
author_sort Fryer, Helen R.
collection PubMed
description During infection with human immunodeficiency virus (HIV), immune pressure from cytotoxic T-lymphocytes (CTLs) selects for viral mutants that confer escape from CTL recognition. These escape variants can be transmitted between individuals where, depending upon their cost to viral fitness and the CTL responses made by the recipient, they may revert. The rates of within-host evolution and their concordant impact upon the rate of spread of escape mutants at the population level are uncertain. Here we present a mathematical model of within-host evolution of escape mutants, transmission of these variants between hosts and subsequent reversion in new hosts. The model is an extension of the well-known SI model of disease transmission and includes three further parameters that describe host immunogenetic heterogeneity and rates of within host viral evolution. We use the model to explain why some escape mutants appear to have stable prevalence whilst others are spreading through the population. Further, we use it to compare diverse datasets on CTL escape, highlighting where different sources agree or disagree on within-host evolutionary rates. The several dozen CTL epitopes we survey from HIV-1 gag, RT and nef reveal a relatively sedate rate of evolution with average rates of escape measured in years and reversion in decades. For many epitopes in HIV, occasional rapid within-host evolution is not reflected in fast evolution at the population level.
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spelling pubmed-29878222010-12-01 Modelling the Evolution and Spread of HIV Immune Escape Mutants Fryer, Helen R. Frater, John Duda, Anna Roberts, Mick G. Phillips, Rodney E. McLean, Angela R. PLoS Pathog Research Article During infection with human immunodeficiency virus (HIV), immune pressure from cytotoxic T-lymphocytes (CTLs) selects for viral mutants that confer escape from CTL recognition. These escape variants can be transmitted between individuals where, depending upon their cost to viral fitness and the CTL responses made by the recipient, they may revert. The rates of within-host evolution and their concordant impact upon the rate of spread of escape mutants at the population level are uncertain. Here we present a mathematical model of within-host evolution of escape mutants, transmission of these variants between hosts and subsequent reversion in new hosts. The model is an extension of the well-known SI model of disease transmission and includes three further parameters that describe host immunogenetic heterogeneity and rates of within host viral evolution. We use the model to explain why some escape mutants appear to have stable prevalence whilst others are spreading through the population. Further, we use it to compare diverse datasets on CTL escape, highlighting where different sources agree or disagree on within-host evolutionary rates. The several dozen CTL epitopes we survey from HIV-1 gag, RT and nef reveal a relatively sedate rate of evolution with average rates of escape measured in years and reversion in decades. For many epitopes in HIV, occasional rapid within-host evolution is not reflected in fast evolution at the population level. Public Library of Science 2010-11-18 /pmc/articles/PMC2987822/ /pubmed/21124991 http://dx.doi.org/10.1371/journal.ppat.1001196 Text en Fryer et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Fryer, Helen R.
Frater, John
Duda, Anna
Roberts, Mick G.
Phillips, Rodney E.
McLean, Angela R.
Modelling the Evolution and Spread of HIV Immune Escape Mutants
title Modelling the Evolution and Spread of HIV Immune Escape Mutants
title_full Modelling the Evolution and Spread of HIV Immune Escape Mutants
title_fullStr Modelling the Evolution and Spread of HIV Immune Escape Mutants
title_full_unstemmed Modelling the Evolution and Spread of HIV Immune Escape Mutants
title_short Modelling the Evolution and Spread of HIV Immune Escape Mutants
title_sort modelling the evolution and spread of hiv immune escape mutants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2987822/
https://www.ncbi.nlm.nih.gov/pubmed/21124991
http://dx.doi.org/10.1371/journal.ppat.1001196
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