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Estimating the individualized HIV-1 genetic barrier to resistance using a nelfinavir fitness landscape

BACKGROUND: Failure on Highly Active Anti-Retroviral Treatment is often accompanied with development of antiviral resistance to one or more drugs included in the treatment. In general, the virus is more likely to develop resistance to drugs with a lower genetic barrier. Previously, we developed a me...

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Autores principales: Theys, Kristof, Deforche, Koen, Beheydt, Gertjan, Moreau, Yves, van Laethem, Kristel, Lemey, Philippe, Camacho, Ricardo J, Rhee, Soo-Yon, Shafer, Robert W, Van Wijngaerden, Eric, Vandamme, Anne-Mieke
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2921410/
https://www.ncbi.nlm.nih.gov/pubmed/20682040
http://dx.doi.org/10.1186/1471-2105-11-409
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author Theys, Kristof
Deforche, Koen
Beheydt, Gertjan
Moreau, Yves
van Laethem, Kristel
Lemey, Philippe
Camacho, Ricardo J
Rhee, Soo-Yon
Shafer, Robert W
Van Wijngaerden, Eric
Vandamme, Anne-Mieke
author_facet Theys, Kristof
Deforche, Koen
Beheydt, Gertjan
Moreau, Yves
van Laethem, Kristel
Lemey, Philippe
Camacho, Ricardo J
Rhee, Soo-Yon
Shafer, Robert W
Van Wijngaerden, Eric
Vandamme, Anne-Mieke
author_sort Theys, Kristof
collection PubMed
description BACKGROUND: Failure on Highly Active Anti-Retroviral Treatment is often accompanied with development of antiviral resistance to one or more drugs included in the treatment. In general, the virus is more likely to develop resistance to drugs with a lower genetic barrier. Previously, we developed a method to reverse engineer, from clinical sequence data, a fitness landscape experienced by HIV-1 under nelfinavir (NFV) treatment. By simulation of evolution over this landscape, the individualized genetic barrier to NFV resistance may be estimated for an isolate. RESULTS: We investigated the association of estimated genetic barrier with risk of development of NFV resistance at virological failure, in 201 patients that were predicted fully susceptible to NFV at baseline, and found that a higher estimated genetic barrier was indeed associated with lower odds for development of resistance at failure (OR 0.62 (0.45 - 0.94), per additional mutation needed, p = .02). CONCLUSIONS: Thus, variation in individualized genetic barrier to NFV resistance may impact effective treatment options available after treatment failure. If similar results apply for other drugs, then estimated genetic barrier may be a new clinical tool for choice of treatment regimen, which allows consideration of available treatment options after virological failure.
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spelling pubmed-29214102010-08-14 Estimating the individualized HIV-1 genetic barrier to resistance using a nelfinavir fitness landscape Theys, Kristof Deforche, Koen Beheydt, Gertjan Moreau, Yves van Laethem, Kristel Lemey, Philippe Camacho, Ricardo J Rhee, Soo-Yon Shafer, Robert W Van Wijngaerden, Eric Vandamme, Anne-Mieke BMC Bioinformatics Research Article BACKGROUND: Failure on Highly Active Anti-Retroviral Treatment is often accompanied with development of antiviral resistance to one or more drugs included in the treatment. In general, the virus is more likely to develop resistance to drugs with a lower genetic barrier. Previously, we developed a method to reverse engineer, from clinical sequence data, a fitness landscape experienced by HIV-1 under nelfinavir (NFV) treatment. By simulation of evolution over this landscape, the individualized genetic barrier to NFV resistance may be estimated for an isolate. RESULTS: We investigated the association of estimated genetic barrier with risk of development of NFV resistance at virological failure, in 201 patients that were predicted fully susceptible to NFV at baseline, and found that a higher estimated genetic barrier was indeed associated with lower odds for development of resistance at failure (OR 0.62 (0.45 - 0.94), per additional mutation needed, p = .02). CONCLUSIONS: Thus, variation in individualized genetic barrier to NFV resistance may impact effective treatment options available after treatment failure. If similar results apply for other drugs, then estimated genetic barrier may be a new clinical tool for choice of treatment regimen, which allows consideration of available treatment options after virological failure. BioMed Central 2010-08-03 /pmc/articles/PMC2921410/ /pubmed/20682040 http://dx.doi.org/10.1186/1471-2105-11-409 Text en Copyright ©2010 Theys et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Theys, Kristof
Deforche, Koen
Beheydt, Gertjan
Moreau, Yves
van Laethem, Kristel
Lemey, Philippe
Camacho, Ricardo J
Rhee, Soo-Yon
Shafer, Robert W
Van Wijngaerden, Eric
Vandamme, Anne-Mieke
Estimating the individualized HIV-1 genetic barrier to resistance using a nelfinavir fitness landscape
title Estimating the individualized HIV-1 genetic barrier to resistance using a nelfinavir fitness landscape
title_full Estimating the individualized HIV-1 genetic barrier to resistance using a nelfinavir fitness landscape
title_fullStr Estimating the individualized HIV-1 genetic barrier to resistance using a nelfinavir fitness landscape
title_full_unstemmed Estimating the individualized HIV-1 genetic barrier to resistance using a nelfinavir fitness landscape
title_short Estimating the individualized HIV-1 genetic barrier to resistance using a nelfinavir fitness landscape
title_sort estimating the individualized hiv-1 genetic barrier to resistance using a nelfinavir fitness landscape
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2921410/
https://www.ncbi.nlm.nih.gov/pubmed/20682040
http://dx.doi.org/10.1186/1471-2105-11-409
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