Control of the HIV-1 Load Varies by Viral Subtype in a Large Cohort of African Adults With Incident HIV-1 Infection
Few human immunodeficiency virus (HIV)–infected persons can maintain low viral levels without therapeutic intervention. We evaluate predictors of spontaneous control of the viral load (hereafter, “viral control”) in a prospective cohort of African adults shortly after HIV infection. Viral control wa...
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creator | Price, Matt A. Rida, Wasima Kilembe, William Karita, Etienne Inambao, Mubiana Ruzagira, Eugene Kamali, Anatoli Sanders, Eduard J. Anzala, Omu Hunter, Eric Allen, Susan Edward, Vinodh A. Wall, Kristin M. Tang, Jianming Fast, Patricia E. Kaleebu, Pontiano Lakhi, Shabir Mutua, Gaudensia Bekker, Linda Gail Abu-Baker, Ggayi Tichacek, Amanda Chetty, Paramesh Latka, Mary H Maenetje, Pholo Makkan, Heeran Kibengo, Freddie Priddy, Fran Gilmour, Jill |
description | Few human immunodeficiency virus (HIV)–infected persons can maintain low viral levels without therapeutic intervention. We evaluate predictors of spontaneous control of the viral load (hereafter, “viral control”) in a prospective cohort of African adults shortly after HIV infection. Viral control was defined as ≥2 consecutively measured viral loads (VLs) of ≤10 000 copies/mL after the estimated date of infection, followed by at least 4 subsequent measurements for which the VL in at least 75% was ≤10 000 copies/mL in the absence of ART. Multivariable logistic regression characterized predictors of viral control. Of 590 eligible volunteers, 107 (18.1%) experienced viral control, of whom 25 (4.2%) maintained a VL of 51–2000 copies/mL, and 5 (0.8%) sustained a VL of ≤50 copies/mL. The median ART-free follow-up time was 3.3 years (range, 0.3–9.7 years). Factors independently associated with control were HIV-1 subtype A (reference, subtype C; adjusted odds ratio [aOR], 2.1 [95% confidence interval {CI}, 1.3–3.5]), female sex (reference, male sex; aOR, 1.8 [95% CI, 1.1–2.8]), and having HLA class I variant allele B*57 (reference, not having this allele; aOR, 1.9 [95% CI, 1.0–3.6]) in a multivariable model that also controlled for age at the time of infection and baseline CD4⁺ T-cell count. We observed strong associations between infecting HIV-1 subtype, HLA type, and sex on viral control in this cohort. HIV-1 subtype is important to consider when testing and designing new therapeutic and prevention technologies, including vaccines. |
doi_str_mv | 10.1093/infdis/jiz127 |
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We evaluate predictors of spontaneous control of the viral load (hereafter, “viral control”) in a prospective cohort of African adults shortly after HIV infection. Viral control was defined as ≥2 consecutively measured viral loads (VLs) of ≤10 000 copies/mL after the estimated date of infection, followed by at least 4 subsequent measurements for which the VL in at least 75% was ≤10 000 copies/mL in the absence of ART. Multivariable logistic regression characterized predictors of viral control. Of 590 eligible volunteers, 107 (18.1%) experienced viral control, of whom 25 (4.2%) maintained a VL of 51–2000 copies/mL, and 5 (0.8%) sustained a VL of ≤50 copies/mL. The median ART-free follow-up time was 3.3 years (range, 0.3–9.7 years). Factors independently associated with control were HIV-1 subtype A (reference, subtype C; adjusted odds ratio [aOR], 2.1 [95% confidence interval {CI}, 1.3–3.5]), female sex (reference, male sex; aOR, 1.8 [95% CI, 1.1–2.8]), and having HLA class I variant allele B*57 (reference, not having this allele; aOR, 1.9 [95% CI, 1.0–3.6]) in a multivariable model that also controlled for age at the time of infection and baseline CD4⁺ T-cell count. We observed strong associations between infecting HIV-1 subtype, HLA type, and sex on viral control in this cohort. HIV-1 subtype is important to consider when testing and designing new therapeutic and prevention technologies, including vaccines.</description><identifier>ISSN: 0022-1899</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1093/infdis/jiz127</identifier><identifier>PMID: 30938435</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Alleles ; Antiretroviral therapy ; CD4 antigen ; Epidemiology ; Histocompatibility antigen HLA ; HIV ; HIV/AIDS ; Human immunodeficiency virus ; Infections ; Lymphocytes T ; Major and Brief Reports ; Sex</subject><ispartof>The Journal of infectious diseases, 2019-07, Vol.220 (3), p.432-441</ispartof><rights>The Author(s) 2019</rights><rights>The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America.</rights><rights>The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c437t-caa70104de639f947201b5792d2bacc134372836266f624bf57bf45b92364cfb3</citedby><cites>FETCH-LOGICAL-c437t-caa70104de639f947201b5792d2bacc134372836266f624bf57bf45b92364cfb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30938435$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Price, Matt A.</creatorcontrib><creatorcontrib>Rida, Wasima</creatorcontrib><creatorcontrib>Kilembe, William</creatorcontrib><creatorcontrib>Karita, Etienne</creatorcontrib><creatorcontrib>Inambao, Mubiana</creatorcontrib><creatorcontrib>Ruzagira, Eugene</creatorcontrib><creatorcontrib>Kamali, Anatoli</creatorcontrib><creatorcontrib>Sanders, Eduard J.</creatorcontrib><creatorcontrib>Anzala, Omu</creatorcontrib><creatorcontrib>Hunter, Eric</creatorcontrib><creatorcontrib>Allen, Susan</creatorcontrib><creatorcontrib>Edward, Vinodh A.</creatorcontrib><creatorcontrib>Wall, Kristin M.</creatorcontrib><creatorcontrib>Tang, Jianming</creatorcontrib><creatorcontrib>Fast, Patricia E.</creatorcontrib><creatorcontrib>Kaleebu, Pontiano</creatorcontrib><creatorcontrib>Lakhi, Shabir</creatorcontrib><creatorcontrib>Mutua, Gaudensia</creatorcontrib><creatorcontrib>Bekker, Linda Gail</creatorcontrib><creatorcontrib>Abu-Baker, Ggayi</creatorcontrib><creatorcontrib>Tichacek, Amanda</creatorcontrib><creatorcontrib>Chetty, Paramesh</creatorcontrib><creatorcontrib>Latka, Mary H</creatorcontrib><creatorcontrib>Maenetje, Pholo</creatorcontrib><creatorcontrib>Makkan, Heeran</creatorcontrib><creatorcontrib>Kibengo, Freddie</creatorcontrib><creatorcontrib>Priddy, Fran</creatorcontrib><creatorcontrib>Gilmour, Jill</creatorcontrib><title>Control of the HIV-1 Load Varies by Viral Subtype in a Large Cohort of African Adults With Incident HIV-1 Infection</title><title>The Journal of infectious diseases</title><addtitle>J Infect Dis</addtitle><description>Few human immunodeficiency virus (HIV)–infected persons can maintain low viral levels without therapeutic intervention. We evaluate predictors of spontaneous control of the viral load (hereafter, “viral control”) in a prospective cohort of African adults shortly after HIV infection. Viral control was defined as ≥2 consecutively measured viral loads (VLs) of ≤10 000 copies/mL after the estimated date of infection, followed by at least 4 subsequent measurements for which the VL in at least 75% was ≤10 000 copies/mL in the absence of ART. Multivariable logistic regression characterized predictors of viral control. Of 590 eligible volunteers, 107 (18.1%) experienced viral control, of whom 25 (4.2%) maintained a VL of 51–2000 copies/mL, and 5 (0.8%) sustained a VL of ≤50 copies/mL. The median ART-free follow-up time was 3.3 years (range, 0.3–9.7 years). 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HIV-1 subtype is important to consider when testing and designing new therapeutic and prevention technologies, including vaccines.</description><subject>Alleles</subject><subject>Antiretroviral therapy</subject><subject>CD4 antigen</subject><subject>Epidemiology</subject><subject>Histocompatibility antigen HLA</subject><subject>HIV</subject><subject>HIV/AIDS</subject><subject>Human immunodeficiency virus</subject><subject>Infections</subject><subject>Lymphocytes T</subject><subject>Major and Brief Reports</subject><subject>Sex</subject><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNpVkc2LUzEUxYMoTh1dulQCrt9Mvl7yshFKUadQcKHWZUjykmlKJ6lJnlD_ejO8TtHVXdzfPfccDgBvMbrBSNLbEP0Yyu0-_MFEPAML3FPRcY7pc7BAiJAOD1JegVel7BFCjHLxElzRdjkw2i9AWaVYczrA5GHdOXi33nYYbpIe4Vbn4Ao0J7gNWR_gt8nU09HBEKGGG53vHVylXcr18Xbpc7A6wuU4HWqBP0PdwXW0YXSxnkXX0TtbQ4qvwQuvD8W9Oc9r8OPzp--ru27z9ct6tdx0llFRO6u1QBix0XEqvWSCIGx6IclIjLYW00aRgXLCueeEGd8L41lvJKGcWW_oNfg46x4n8-BG26y0HOqYw4POJ5V0UP9vYtip-_RbcY6o5EMT-HAWyOnX5EpV-zTl2DwrwthABCUSN6qbKZtTKdn5yweM1GNHau5IzR01_v2_ti70UykNeDcD-1JTvuwJF0yilu4v_PiXuw</recordid><startdate>20190702</startdate><enddate>20190702</enddate><creator>Price, Matt A.</creator><creator>Rida, Wasima</creator><creator>Kilembe, William</creator><creator>Karita, Etienne</creator><creator>Inambao, Mubiana</creator><creator>Ruzagira, Eugene</creator><creator>Kamali, Anatoli</creator><creator>Sanders, Eduard J.</creator><creator>Anzala, Omu</creator><creator>Hunter, Eric</creator><creator>Allen, Susan</creator><creator>Edward, Vinodh A.</creator><creator>Wall, Kristin M.</creator><creator>Tang, Jianming</creator><creator>Fast, Patricia E.</creator><creator>Kaleebu, Pontiano</creator><creator>Lakhi, Shabir</creator><creator>Mutua, Gaudensia</creator><creator>Bekker, Linda Gail</creator><creator>Abu-Baker, Ggayi</creator><creator>Tichacek, Amanda</creator><creator>Chetty, Paramesh</creator><creator>Latka, Mary H</creator><creator>Maenetje, Pholo</creator><creator>Makkan, Heeran</creator><creator>Kibengo, Freddie</creator><creator>Priddy, Fran</creator><creator>Gilmour, Jill</creator><general>Oxford University Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>5PM</scope></search><sort><creationdate>20190702</creationdate><title>Control of the HIV-1 Load Varies by Viral Subtype in a Large Cohort of African Adults With Incident HIV-1 Infection</title><author>Price, Matt A. ; 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We evaluate predictors of spontaneous control of the viral load (hereafter, “viral control”) in a prospective cohort of African adults shortly after HIV infection. Viral control was defined as ≥2 consecutively measured viral loads (VLs) of ≤10 000 copies/mL after the estimated date of infection, followed by at least 4 subsequent measurements for which the VL in at least 75% was ≤10 000 copies/mL in the absence of ART. Multivariable logistic regression characterized predictors of viral control. Of 590 eligible volunteers, 107 (18.1%) experienced viral control, of whom 25 (4.2%) maintained a VL of 51–2000 copies/mL, and 5 (0.8%) sustained a VL of ≤50 copies/mL. The median ART-free follow-up time was 3.3 years (range, 0.3–9.7 years). Factors independently associated with control were HIV-1 subtype A (reference, subtype C; adjusted odds ratio [aOR], 2.1 [95% confidence interval {CI}, 1.3–3.5]), female sex (reference, male sex; aOR, 1.8 [95% CI, 1.1–2.8]), and having HLA class I variant allele B*57 (reference, not having this allele; aOR, 1.9 [95% CI, 1.0–3.6]) in a multivariable model that also controlled for age at the time of infection and baseline CD4⁺ T-cell count. We observed strong associations between infecting HIV-1 subtype, HLA type, and sex on viral control in this cohort. HIV-1 subtype is important to consider when testing and designing new therapeutic and prevention technologies, including vaccines.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>30938435</pmid><doi>10.1093/infdis/jiz127</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alleles Antiretroviral therapy CD4 antigen Epidemiology Histocompatibility antigen HLA HIV HIV/AIDS Human immunodeficiency virus Infections Lymphocytes T Major and Brief Reports Sex |
title | Control of the HIV-1 Load Varies by Viral Subtype in a Large Cohort of African Adults With Incident HIV-1 Infection |
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