Mutations related to Antiretroviral Resistance identified by ultra-deep sequencing in HIV-1 infected children under Structured Interruptions of HAART
Although Structured Treatment Interruptions (STI) are currently not considered an alternative strategy for antiretroviral treatment, their true benefits and limitations have not been fully established. Some studies suggest the possibility of improving the quality of life of patients with this strate...
| Authors: | , , , , , , , , , , , , , , |
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| Format: | article |
| Publication Date: | 2016 |
| Country: | España |
| Institution: | Universitat Autònoma de Barcelona |
| Repository: | Dipòsit Digital de Documents de la UAB |
| Language: | English |
| OAI Identifier: | oai:ddd.uab.cat:174694 |
| Online Access: | https://ddd.uab.cat/record/174694 https://dx.doi.org/urn:doi:10.1371/journal.pone.0147591 |
| Access Level: | Open access |
| Keyword: | SIDA VIH (Virus) Antiretroviral resistance Structured interruptions of HAART Structured Treatment Interruptions (STI) |
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Mutations related to Antiretroviral Resistance identified by ultra-deep sequencing in HIV-1 infected children under Structured Interruptions of HAARTVázquez Guillén, José ManuelPalacios Saucedo, Gerardo C.Rivera Morales, Lydia G.García Campos, JorgeOrtiz López, RocíoNoguera-Julian, Marc|||0000-0002-6194-1395Paredes, Roger|||0000-0002-6553-691XVielma Ramírez, Herlinda J.Ramírez, TeresaChávez García, MarcelinoLópez Guillén, PauloBriones Lara, EvangelinaSánchez Sánchez, Luz M.Vázquez Martínez, Carlos A.Rodríguez Padilla, CristinaSIDAVIH (Virus)Antiretroviral resistanceStructured interruptions of HAARTStructured Treatment Interruptions (STI)Although Structured Treatment Interruptions (STI) are currently not considered an alternative strategy for antiretroviral treatment, their true benefits and limitations have not been fully established. Some studies suggest the possibility of improving the quality of life of patients with this strategy; however, the information that has been obtained corresponds mostly to studies conducted in adults, with a lack of knowledge about its impact on children. Furthermore, mutations associated with antiretroviral resistance could be selected due to sub-therapeutic levels of HAART at each interruption period. Genotyping methods to determine the resistance profiles of the infecting viruses have become increasingly important for the management of patients under STI, thus low-abundance antiretroviral drug-resistant mutations (DRM's) at levels under limit of detection of conventional genotyping (<20% of quasispecies) could increase the risk of virologic failure. In this work, we analyzed the protease and reverse transcriptase regions of the pol gene by ultra-deep sequencing in pediatric patients under STI with the aim of determining the presence of high- and low-abundance DRM's in the viral rebounds generated by the STI. High-abundance mutations in protease and high- and low-abundance mutations in reverse transcriptase were detected but no one of these are directly associated with resistance to antiretroviral drugs. The results could suggest that the evaluated STI program is virologically safe, but strict and carefully planned studies, with greater numbers of patients and interruption/restart cycles, are still needed to evaluate the selection of DRM's during STI. 22016-01-0120162016-01-01Articlehttp://purl.org/coar/resource_type/c_6501VoRhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleapplication/pdfhttps://ddd.uab.cat/record/174694https://dx.doi.org/urn:doi:10.1371/journal.pone.0147591reponame:Dipòsit Digital de Documents de la UABinstname:Universitat Autònoma de BarcelonaInglésengopen accesshttp://purl.org/coar/access_right/c_abf2Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original.https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessoai:ddd.uab.cat:1746942026-06-06T12:50:31Z |
| dc.title.none.fl_str_mv |
Mutations related to Antiretroviral Resistance identified by ultra-deep sequencing in HIV-1 infected children under Structured Interruptions of HAART |
| title |
Mutations related to Antiretroviral Resistance identified by ultra-deep sequencing in HIV-1 infected children under Structured Interruptions of HAART |
| spellingShingle |
Mutations related to Antiretroviral Resistance identified by ultra-deep sequencing in HIV-1 infected children under Structured Interruptions of HAART Vázquez Guillén, José Manuel SIDA VIH (Virus) Antiretroviral resistance Structured interruptions of HAART Structured Treatment Interruptions (STI) |
| title_short |
Mutations related to Antiretroviral Resistance identified by ultra-deep sequencing in HIV-1 infected children under Structured Interruptions of HAART |
| title_full |
Mutations related to Antiretroviral Resistance identified by ultra-deep sequencing in HIV-1 infected children under Structured Interruptions of HAART |
| title_fullStr |
Mutations related to Antiretroviral Resistance identified by ultra-deep sequencing in HIV-1 infected children under Structured Interruptions of HAART |
| title_full_unstemmed |
Mutations related to Antiretroviral Resistance identified by ultra-deep sequencing in HIV-1 infected children under Structured Interruptions of HAART |
| title_sort |
Mutations related to Antiretroviral Resistance identified by ultra-deep sequencing in HIV-1 infected children under Structured Interruptions of HAART |
| dc.creator.none.fl_str_mv |
Vázquez Guillén, José Manuel Palacios Saucedo, Gerardo C. Rivera Morales, Lydia G. García Campos, Jorge Ortiz López, Rocío Noguera-Julian, Marc|||0000-0002-6194-1395 Paredes, Roger|||0000-0002-6553-691X Vielma Ramírez, Herlinda J. Ramírez, Teresa Chávez García, Marcelino López Guillén, Paulo Briones Lara, Evangelina Sánchez Sánchez, Luz M. Vázquez Martínez, Carlos A. Rodríguez Padilla, Cristina |
| author |
Vázquez Guillén, José Manuel |
| author_facet |
Vázquez Guillén, José Manuel Palacios Saucedo, Gerardo C. Rivera Morales, Lydia G. García Campos, Jorge Ortiz López, Rocío Noguera-Julian, Marc|||0000-0002-6194-1395 Paredes, Roger|||0000-0002-6553-691X Vielma Ramírez, Herlinda J. Ramírez, Teresa Chávez García, Marcelino López Guillén, Paulo Briones Lara, Evangelina Sánchez Sánchez, Luz M. Vázquez Martínez, Carlos A. Rodríguez Padilla, Cristina |
| author_role |
author |
| author2 |
Palacios Saucedo, Gerardo C. Rivera Morales, Lydia G. García Campos, Jorge Ortiz López, Rocío Noguera-Julian, Marc|||0000-0002-6194-1395 Paredes, Roger|||0000-0002-6553-691X Vielma Ramírez, Herlinda J. Ramírez, Teresa Chávez García, Marcelino López Guillén, Paulo Briones Lara, Evangelina Sánchez Sánchez, Luz M. Vázquez Martínez, Carlos A. Rodríguez Padilla, Cristina |
| author2_role |
author author author author author author author author author author author author author author |
| dc.subject.none.fl_str_mv |
SIDA VIH (Virus) Antiretroviral resistance Structured interruptions of HAART Structured Treatment Interruptions (STI) |
| topic |
SIDA VIH (Virus) Antiretroviral resistance Structured interruptions of HAART Structured Treatment Interruptions (STI) |
| description |
Although Structured Treatment Interruptions (STI) are currently not considered an alternative strategy for antiretroviral treatment, their true benefits and limitations have not been fully established. Some studies suggest the possibility of improving the quality of life of patients with this strategy; however, the information that has been obtained corresponds mostly to studies conducted in adults, with a lack of knowledge about its impact on children. Furthermore, mutations associated with antiretroviral resistance could be selected due to sub-therapeutic levels of HAART at each interruption period. Genotyping methods to determine the resistance profiles of the infecting viruses have become increasingly important for the management of patients under STI, thus low-abundance antiretroviral drug-resistant mutations (DRM's) at levels under limit of detection of conventional genotyping (<20% of quasispecies) could increase the risk of virologic failure. In this work, we analyzed the protease and reverse transcriptase regions of the pol gene by ultra-deep sequencing in pediatric patients under STI with the aim of determining the presence of high- and low-abundance DRM's in the viral rebounds generated by the STI. High-abundance mutations in protease and high- and low-abundance mutations in reverse transcriptase were detected but no one of these are directly associated with resistance to antiretroviral drugs. The results could suggest that the evaluated STI program is virologically safe, but strict and carefully planned studies, with greater numbers of patients and interruption/restart cycles, are still needed to evaluate the selection of DRM's during STI. |
| publishDate |
2016 |
| dc.date.none.fl_str_mv |
2 2016-01-01 2016 2016-01-01 |
| dc.type.none.fl_str_mv |
Article http://purl.org/coar/resource_type/c_6501 VoR http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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info:eu-repo/semantics/article |
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article |
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https://ddd.uab.cat/record/174694 https://dx.doi.org/urn:doi:10.1371/journal.pone.0147591 |
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https://ddd.uab.cat/record/174694 https://dx.doi.org/urn:doi:10.1371/journal.pone.0147591 |
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Inglés eng |
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Inglés |
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eng |
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open access http://purl.org/coar/access_right/c_abf2 https://creativecommons.org/licenses/by/4.0/ |
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info:eu-repo/semantics/openAccess |
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open access http://purl.org/coar/access_right/c_abf2 https://creativecommons.org/licenses/by/4.0/ |
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