Genotypic resistance and HIV-1 subtype in Brazilian children on dual and triple combination therapy
Background: Antiretroviral therapy is provided by the Brazilian Ministry of Health to eligible HIV-infected individuals. Based on clinical and immunological classification, the Brazilian guidelines recommend dual or triple therapy for children. However, the development of drug-resistant strains or p...
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creator | Machado, Elizabeth S Lambert, John S Watson, Douglas C Afonso, Adriana O da Cunha, Silvia M Nogueira, Susie A Caride, Elena Oliveira, Ricardo H Sill, Anne M DeVico, Anthony Tanuri, Amilcar |
description | Background: Antiretroviral therapy is provided by the Brazilian Ministry of Health to eligible HIV-infected individuals. Based on clinical and immunological classification, the Brazilian guidelines recommend dual or triple therapy for children. However, the development of drug-resistant strains or poor adherence to therapy could impact the efficacy of this approach.
Objectives: We examined relationships between RNA levels, CD4+ T-cell counts, treatment history, and the prevalence of drug-resistant variants in a cohort of HIV-1-infected children in Rio de Janeiro, Brazil.
Study design: Direct sequencing of reverse transcriptase and protease genes from plasma was performed. Virologic and CD4+ T-cell counts responses to therapy were assessed by changes in HIV-1 RNA levels and CD4+ T-cell counts from baseline.
Results: Thirty-seven patients were receiving dual therapy and 38 were on triple therapy at enrollment, segregated by antiretroviral history. Both groups had a higher increase in CD4+ T cell counts and a lower viral load in pre-treatment antiretroviral-naı̈ve subjects. Notably, there was a direct correlation between the higher frequencies of drug-resistance mutations and cross-resistance with previous usage of antiretroviral (ARV) therapy in both groups. Non-B subtypes isolates were found in 21.3% of samples. A smaller increase in CD4+ T cell counts was found between non-B subtypes when compared to B-subtypes.
Conclusions: These results suggest that less immunological recovery and a higher number of mutations related to drug resistance were associated with previous usage of ARV and consequent higher time under drug selective pressure in these HIV-infected Brazilian children. These facts suggest the preferential use of triple drug combination as first line regimen in children. |
doi_str_mv | 10.1016/j.jcv.2003.08.001 |
format | Article |
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Objectives: We examined relationships between RNA levels, CD4+ T-cell counts, treatment history, and the prevalence of drug-resistant variants in a cohort of HIV-1-infected children in Rio de Janeiro, Brazil.
Study design: Direct sequencing of reverse transcriptase and protease genes from plasma was performed. Virologic and CD4+ T-cell counts responses to therapy were assessed by changes in HIV-1 RNA levels and CD4+ T-cell counts from baseline.
Results: Thirty-seven patients were receiving dual therapy and 38 were on triple therapy at enrollment, segregated by antiretroviral history. Both groups had a higher increase in CD4+ T cell counts and a lower viral load in pre-treatment antiretroviral-naı̈ve subjects. Notably, there was a direct correlation between the higher frequencies of drug-resistance mutations and cross-resistance with previous usage of antiretroviral (ARV) therapy in both groups. Non-B subtypes isolates were found in 21.3% of samples. A smaller increase in CD4+ T cell counts was found between non-B subtypes when compared to B-subtypes.
Conclusions: These results suggest that less immunological recovery and a higher number of mutations related to drug resistance were associated with previous usage of ARV and consequent higher time under drug selective pressure in these HIV-infected Brazilian children. These facts suggest the preferential use of triple drug combination as first line regimen in children.</description><identifier>ISSN: 1386-6532</identifier><identifier>EISSN: 1873-5967</identifier><identifier>DOI: 10.1016/j.jcv.2003.08.001</identifier><identifier>PMID: 15072750</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Adolescent ; Anti-HIV Agents - pharmacology ; Anti-HIV Agents - therapeutic use ; Biological and medical sciences ; Brazil ; CD4 Lymphocyte Count ; Child ; Child, Preschool ; Combination therapy ; DNA, Complementary - chemistry ; DNA, Complementary - isolation & purification ; Drug Resistance, Viral - genetics ; Drug Therapy, Combination ; Evolution, Molecular ; Female ; Fundamental and applied biological sciences. Psychology ; Genotypic resistance ; HIV Infections - drug therapy ; HIV Infections - immunology ; HIV Infections - virology ; HIV Protease - genetics ; HIV Reverse Transcriptase - genetics ; HIV-1 - drug effects ; HIV-1 - genetics ; HIV-1 - isolation & purification ; HIV-1 subtype ; Human immunodeficiency virus ; Human immunodeficiency virus 1 ; Human viral diseases ; Humans ; Infant ; Infectious diseases ; Male ; Medical sciences ; Microbiology ; Miscellaneous ; Molecular Sequence Data ; Mutation, Missense ; RNA, Viral - blood ; RNA, Viral - isolation & purification ; Selection, Genetic ; Sequence Analysis, DNA ; Viral diseases ; Viral diseases of the lymphoid tissue and the blood. Aids ; Viral Load ; Viremia ; Virology</subject><ispartof>Journal of clinical virology, 2004-05, Vol.30 (1), p.24-31</ispartof><rights>2003 Elsevier B.V.</rights><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-e6c371e830e3d3ad3240b4c043c086ce2a9bb0f0036b849d06833307c25a928a3</citedby><cites>FETCH-LOGICAL-c412t-e6c371e830e3d3ad3240b4c043c086ce2a9bb0f0036b849d06833307c25a928a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jcv.2003.08.001$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15627069$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15072750$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Machado, Elizabeth S</creatorcontrib><creatorcontrib>Lambert, John S</creatorcontrib><creatorcontrib>Watson, Douglas C</creatorcontrib><creatorcontrib>Afonso, Adriana O</creatorcontrib><creatorcontrib>da Cunha, Silvia M</creatorcontrib><creatorcontrib>Nogueira, Susie A</creatorcontrib><creatorcontrib>Caride, Elena</creatorcontrib><creatorcontrib>Oliveira, Ricardo H</creatorcontrib><creatorcontrib>Sill, Anne M</creatorcontrib><creatorcontrib>DeVico, Anthony</creatorcontrib><creatorcontrib>Tanuri, Amilcar</creatorcontrib><title>Genotypic resistance and HIV-1 subtype in Brazilian children on dual and triple combination therapy</title><title>Journal of clinical virology</title><addtitle>J Clin Virol</addtitle><description>Background: Antiretroviral therapy is provided by the Brazilian Ministry of Health to eligible HIV-infected individuals. Based on clinical and immunological classification, the Brazilian guidelines recommend dual or triple therapy for children. However, the development of drug-resistant strains or poor adherence to therapy could impact the efficacy of this approach.
Objectives: We examined relationships between RNA levels, CD4+ T-cell counts, treatment history, and the prevalence of drug-resistant variants in a cohort of HIV-1-infected children in Rio de Janeiro, Brazil.
Study design: Direct sequencing of reverse transcriptase and protease genes from plasma was performed. Virologic and CD4+ T-cell counts responses to therapy were assessed by changes in HIV-1 RNA levels and CD4+ T-cell counts from baseline.
Results: Thirty-seven patients were receiving dual therapy and 38 were on triple therapy at enrollment, segregated by antiretroviral history. Both groups had a higher increase in CD4+ T cell counts and a lower viral load in pre-treatment antiretroviral-naı̈ve subjects. Notably, there was a direct correlation between the higher frequencies of drug-resistance mutations and cross-resistance with previous usage of antiretroviral (ARV) therapy in both groups. Non-B subtypes isolates were found in 21.3% of samples. A smaller increase in CD4+ T cell counts was found between non-B subtypes when compared to B-subtypes.
Conclusions: These results suggest that less immunological recovery and a higher number of mutations related to drug resistance were associated with previous usage of ARV and consequent higher time under drug selective pressure in these HIV-infected Brazilian children. These facts suggest the preferential use of triple drug combination as first line regimen in children.</description><subject>Adolescent</subject><subject>Anti-HIV Agents - pharmacology</subject><subject>Anti-HIV Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Brazil</subject><subject>CD4 Lymphocyte Count</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Combination therapy</subject><subject>DNA, Complementary - chemistry</subject><subject>DNA, Complementary - isolation & purification</subject><subject>Drug Resistance, Viral - genetics</subject><subject>Drug Therapy, Combination</subject><subject>Evolution, Molecular</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genotypic resistance</subject><subject>HIV Infections - drug therapy</subject><subject>HIV Infections - immunology</subject><subject>HIV Infections - virology</subject><subject>HIV Protease - genetics</subject><subject>HIV Reverse Transcriptase - genetics</subject><subject>HIV-1 - drug effects</subject><subject>HIV-1 - genetics</subject><subject>HIV-1 - isolation & purification</subject><subject>HIV-1 subtype</subject><subject>Human immunodeficiency virus</subject><subject>Human immunodeficiency virus 1</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infant</subject><subject>Infectious diseases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>Molecular Sequence Data</subject><subject>Mutation, Missense</subject><subject>RNA, Viral - blood</subject><subject>RNA, Viral - isolation & purification</subject><subject>Selection, Genetic</subject><subject>Sequence Analysis, DNA</subject><subject>Viral diseases</subject><subject>Viral diseases of the lymphoid tissue and the blood. Aids</subject><subject>Viral Load</subject><subject>Viremia</subject><subject>Virology</subject><issn>1386-6532</issn><issn>1873-5967</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9r3DAQxUVpaZJNP0AvRZfmZnck2ZJMT01o_kCglzZXIUuzRItXdiU7sPn0UboLySk9zcD85jHzHiGfGdQMmPy2qTfuoeYAogZdA7B35JhpJaq2k-p96YWWlWwFPyInOW8K0IpGfSRHrAXFVQvHxF1hHOfdFBxNmEOebXRIbfT0-uauYjQvfZkiDZGeJ_sYhmAjdfdh8AkjHSP1ix3-8XMK04DUjds-RDuHMpvvMdlpd0o-rO2Q8dOhrsify5-_L66r219XNxc_bivXMD5XKJ1QDLUAFF5YL3gDfeOgEQ60dMht1_ewLt_KXjedB6mFEKAcb23HtRUrcrbXndL4d8E8m23IDofBRhyXbBTTrNFc_hdkGgDaor4ibA-6NOaccG2mFLY27QwD8xyB2ZgSgXmOwIA2xeGy8-UgvvRb9C8bB88L8PUA2OzssE7F8pBfcZIrkF3hvu85LJ49BEwmu4AlHh8Sutn4MbxxxhMmNKMD</recordid><startdate>20040501</startdate><enddate>20040501</enddate><creator>Machado, Elizabeth S</creator><creator>Lambert, John S</creator><creator>Watson, Douglas C</creator><creator>Afonso, Adriana O</creator><creator>da Cunha, Silvia M</creator><creator>Nogueira, Susie A</creator><creator>Caride, Elena</creator><creator>Oliveira, Ricardo H</creator><creator>Sill, Anne M</creator><creator>DeVico, Anthony</creator><creator>Tanuri, Amilcar</creator><general>Elsevier B.V</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20040501</creationdate><title>Genotypic resistance and HIV-1 subtype in Brazilian children on dual and triple combination therapy</title><author>Machado, Elizabeth S ; Lambert, John S ; Watson, Douglas C ; Afonso, Adriana O ; da Cunha, Silvia M ; Nogueira, Susie A ; Caride, Elena ; Oliveira, Ricardo H ; Sill, Anne M ; DeVico, Anthony ; Tanuri, Amilcar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c412t-e6c371e830e3d3ad3240b4c043c086ce2a9bb0f0036b849d06833307c25a928a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adolescent</topic><topic>Anti-HIV Agents - pharmacology</topic><topic>Anti-HIV Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Brazil</topic><topic>CD4 Lymphocyte Count</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Combination therapy</topic><topic>DNA, Complementary - chemistry</topic><topic>DNA, Complementary - isolation & purification</topic><topic>Drug Resistance, Viral - genetics</topic><topic>Drug Therapy, Combination</topic><topic>Evolution, Molecular</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genotypic resistance</topic><topic>HIV Infections - drug therapy</topic><topic>HIV Infections - immunology</topic><topic>HIV Infections - virology</topic><topic>HIV Protease - genetics</topic><topic>HIV Reverse Transcriptase - genetics</topic><topic>HIV-1 - drug effects</topic><topic>HIV-1 - genetics</topic><topic>HIV-1 - isolation & purification</topic><topic>HIV-1 subtype</topic><topic>Human immunodeficiency virus</topic><topic>Human immunodeficiency virus 1</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infant</topic><topic>Infectious diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>Molecular Sequence Data</topic><topic>Mutation, Missense</topic><topic>RNA, Viral - blood</topic><topic>RNA, Viral - isolation & purification</topic><topic>Selection, Genetic</topic><topic>Sequence Analysis, DNA</topic><topic>Viral diseases</topic><topic>Viral diseases of the lymphoid tissue and the blood. Aids</topic><topic>Viral Load</topic><topic>Viremia</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Machado, Elizabeth S</creatorcontrib><creatorcontrib>Lambert, John S</creatorcontrib><creatorcontrib>Watson, Douglas C</creatorcontrib><creatorcontrib>Afonso, Adriana O</creatorcontrib><creatorcontrib>da Cunha, Silvia M</creatorcontrib><creatorcontrib>Nogueira, Susie A</creatorcontrib><creatorcontrib>Caride, Elena</creatorcontrib><creatorcontrib>Oliveira, Ricardo H</creatorcontrib><creatorcontrib>Sill, Anne M</creatorcontrib><creatorcontrib>DeVico, Anthony</creatorcontrib><creatorcontrib>Tanuri, Amilcar</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of clinical virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Machado, Elizabeth S</au><au>Lambert, John S</au><au>Watson, Douglas C</au><au>Afonso, Adriana O</au><au>da Cunha, Silvia M</au><au>Nogueira, Susie A</au><au>Caride, Elena</au><au>Oliveira, Ricardo H</au><au>Sill, Anne M</au><au>DeVico, Anthony</au><au>Tanuri, Amilcar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genotypic resistance and HIV-1 subtype in Brazilian children on dual and triple combination therapy</atitle><jtitle>Journal of clinical virology</jtitle><addtitle>J Clin Virol</addtitle><date>2004-05-01</date><risdate>2004</risdate><volume>30</volume><issue>1</issue><spage>24</spage><epage>31</epage><pages>24-31</pages><issn>1386-6532</issn><eissn>1873-5967</eissn><abstract>Background: Antiretroviral therapy is provided by the Brazilian Ministry of Health to eligible HIV-infected individuals. Based on clinical and immunological classification, the Brazilian guidelines recommend dual or triple therapy for children. However, the development of drug-resistant strains or poor adherence to therapy could impact the efficacy of this approach.
Objectives: We examined relationships between RNA levels, CD4+ T-cell counts, treatment history, and the prevalence of drug-resistant variants in a cohort of HIV-1-infected children in Rio de Janeiro, Brazil.
Study design: Direct sequencing of reverse transcriptase and protease genes from plasma was performed. Virologic and CD4+ T-cell counts responses to therapy were assessed by changes in HIV-1 RNA levels and CD4+ T-cell counts from baseline.
Results: Thirty-seven patients were receiving dual therapy and 38 were on triple therapy at enrollment, segregated by antiretroviral history. Both groups had a higher increase in CD4+ T cell counts and a lower viral load in pre-treatment antiretroviral-naı̈ve subjects. Notably, there was a direct correlation between the higher frequencies of drug-resistance mutations and cross-resistance with previous usage of antiretroviral (ARV) therapy in both groups. Non-B subtypes isolates were found in 21.3% of samples. A smaller increase in CD4+ T cell counts was found between non-B subtypes when compared to B-subtypes.
Conclusions: These results suggest that less immunological recovery and a higher number of mutations related to drug resistance were associated with previous usage of ARV and consequent higher time under drug selective pressure in these HIV-infected Brazilian children. These facts suggest the preferential use of triple drug combination as first line regimen in children.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>15072750</pmid><doi>10.1016/j.jcv.2003.08.001</doi><tpages>8</tpages></addata></record> |
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subjects | Adolescent Anti-HIV Agents - pharmacology Anti-HIV Agents - therapeutic use Biological and medical sciences Brazil CD4 Lymphocyte Count Child Child, Preschool Combination therapy DNA, Complementary - chemistry DNA, Complementary - isolation & purification Drug Resistance, Viral - genetics Drug Therapy, Combination Evolution, Molecular Female Fundamental and applied biological sciences. Psychology Genotypic resistance HIV Infections - drug therapy HIV Infections - immunology HIV Infections - virology HIV Protease - genetics HIV Reverse Transcriptase - genetics HIV-1 - drug effects HIV-1 - genetics HIV-1 - isolation & purification HIV-1 subtype Human immunodeficiency virus Human immunodeficiency virus 1 Human viral diseases Humans Infant Infectious diseases Male Medical sciences Microbiology Miscellaneous Molecular Sequence Data Mutation, Missense RNA, Viral - blood RNA, Viral - isolation & purification Selection, Genetic Sequence Analysis, DNA Viral diseases Viral diseases of the lymphoid tissue and the blood. Aids Viral Load Viremia Virology |
title | Genotypic resistance and HIV-1 subtype in Brazilian children on dual and triple combination therapy |
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