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Broad CTL Response in Early HIV Infection Drives Multiple Concurrent CTL Escapes
Recent studies have highlighted the ability of HIV to escape from cytotoxic T lymphocyte (CTL) responses that concurrently target multiple viral epitopes. Yet, the viral dynamics involved in such escape are incompletely understood. Previous analyses have made several strong assumptions regarding HIV...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4624722/ https://www.ncbi.nlm.nih.gov/pubmed/26506433 http://dx.doi.org/10.1371/journal.pcbi.1004492 |
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author | Leviyang, Sivan Ganusov, Vitaly V. |
author_facet | Leviyang, Sivan Ganusov, Vitaly V. |
author_sort | Leviyang, Sivan |
collection | PubMed |
description | Recent studies have highlighted the ability of HIV to escape from cytotoxic T lymphocyte (CTL) responses that concurrently target multiple viral epitopes. Yet, the viral dynamics involved in such escape are incompletely understood. Previous analyses have made several strong assumptions regarding HIV escape from CTL responses such as independent or non-concurrent escape from individual CTL responses. Using experimental data from evolution of HIV half genomes in four patients we observe concurrent viral escape from multiple CTL responses during early infection (first 100 days of infection), providing confirmation of a recent result found in a study of one HIV-infected patient. We show that current methods of estimating CTL escape rates, based on the assumption of independent escapes, are biased and perform poorly when CTL escape proceeds concurrently at multiple epitopes. We propose a new method for analyzing longitudinal sequence data to estimate the rate of CTL escape across multiple epitopes; this method involves few parameters and performs well in simulation studies. By applying our novel method to experimental data, we find that concurrent multiple escapes occur at rates between 0.03 and 0.4 day(−1), a relatively broad range that reflects uncertainty due to sparse sampling and wide ranges of parameter values. However, we show that concurrent escape at rates 0.1–0.2 day(−1) across multiple epitopes is consistent with our patient datasets. |
format | Online Article Text |
id | pubmed-4624722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-46247222015-11-06 Broad CTL Response in Early HIV Infection Drives Multiple Concurrent CTL Escapes Leviyang, Sivan Ganusov, Vitaly V. PLoS Comput Biol Research Article Recent studies have highlighted the ability of HIV to escape from cytotoxic T lymphocyte (CTL) responses that concurrently target multiple viral epitopes. Yet, the viral dynamics involved in such escape are incompletely understood. Previous analyses have made several strong assumptions regarding HIV escape from CTL responses such as independent or non-concurrent escape from individual CTL responses. Using experimental data from evolution of HIV half genomes in four patients we observe concurrent viral escape from multiple CTL responses during early infection (first 100 days of infection), providing confirmation of a recent result found in a study of one HIV-infected patient. We show that current methods of estimating CTL escape rates, based on the assumption of independent escapes, are biased and perform poorly when CTL escape proceeds concurrently at multiple epitopes. We propose a new method for analyzing longitudinal sequence data to estimate the rate of CTL escape across multiple epitopes; this method involves few parameters and performs well in simulation studies. By applying our novel method to experimental data, we find that concurrent multiple escapes occur at rates between 0.03 and 0.4 day(−1), a relatively broad range that reflects uncertainty due to sparse sampling and wide ranges of parameter values. However, we show that concurrent escape at rates 0.1–0.2 day(−1) across multiple epitopes is consistent with our patient datasets. Public Library of Science 2015-10-27 /pmc/articles/PMC4624722/ /pubmed/26506433 http://dx.doi.org/10.1371/journal.pcbi.1004492 Text en © 2015 Leviyang, Ganusov 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 Leviyang, Sivan Ganusov, Vitaly V. Broad CTL Response in Early HIV Infection Drives Multiple Concurrent CTL Escapes |
title | Broad CTL Response in Early HIV Infection Drives Multiple Concurrent CTL Escapes |
title_full | Broad CTL Response in Early HIV Infection Drives Multiple Concurrent CTL Escapes |
title_fullStr | Broad CTL Response in Early HIV Infection Drives Multiple Concurrent CTL Escapes |
title_full_unstemmed | Broad CTL Response in Early HIV Infection Drives Multiple Concurrent CTL Escapes |
title_short | Broad CTL Response in Early HIV Infection Drives Multiple Concurrent CTL Escapes |
title_sort | broad ctl response in early hiv infection drives multiple concurrent ctl escapes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4624722/ https://www.ncbi.nlm.nih.gov/pubmed/26506433 http://dx.doi.org/10.1371/journal.pcbi.1004492 |
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