17 research outputs found

    Immunologic response in treatment-naĂŻve HIV-2-infected patients:the IeDEA West Africa cohort

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    Introduction: Response to antiretroviral therapy (ART) among individuals infected with HIV-2 is poorly described. We compared the immunological response among patients treated with three nucleoside reverse-transcriptase inhibitors (NRTIs) to boosted protease inhibitor (PI) and unboosted PI-based regimens in West Africa. Methods: This prospective cohort study enrolled treatment-naïve HIV-2-infected patients within the International Epidemiological Databases to Evaluate AIDS collaboration in West Africa. We used mixed models to compare the CD4 count response to treatment over 12 months between regimens. Results: Of 422 HIV-2-infected patients, 285 (67.5%) were treated with a boosted PI-based regimen, 104 (24.6%) with an unboosted PI-based regimen and 33 (7.8%) with three NRTIs. Treatment groups were comparable with regard to gender (54.5% female) and median age at ART initiation (45.3 years; interquartile range 38.3 to 51.8). Treatment groups differed by clinical stage (21.2%, 16.8% and 17.3% at CDC Stage C or World Health Organization Stage IV for the triple NRTI, boosted PI and unboosted PI groups, respectively, p=0.02), median length of follow-up (12.9, 17.7 and 44.0 months for the triple NRTI, the boosted PI and the unboosted PI groups, respectively, p<0.001) and baseline median CD4 count (192, 173 and 129 cells/”l in the triple NRTI, the boosted PI and the unboosted PI-based regimen groups, respectively, p=0.003). CD4 count recovery at 12 months was higher for patients treated with boosted PI-based regimens than those treated with three NRTIs or with unboosted PI-based regimens (191 cells/”l, 95% CI 142 to 241; 110 cells/”l, 95% CI 29 to 192; 133 cells/”l, 95% CI 80 to 186, respectively, p=0.004). Conclusions: In this observational study using African data, boosted PI-containing regimens had better immunological response compared to triple NRTI combinations and unboosted PI-based regimens at 12 months. A randomized clinical trial is still required to determine the best initial regimen for treating HIV-2 infected patients

    EBioMedicine

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    Background High HIV-1 DNA levels in peripheral blood mononuclear cells (PBMC) were associated with a higher risk of severe morbidity and a faster decline in CD4 count in ART-naive patients. We report the association between HIV-1 DNA and mortality in HIV-infected adults in a trial of early ART in West Africa. Methods In the Temprano trial, HIV-infected adults were randomly assigned to start ART immediately or defer ART. After trial termination, HIV-1 DNA was measured in whole blood samples frozen at baseline. We analyzed the association between baseline PBMC HIV-1 DNA and long-term mortality

    Clin Infect Dis

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    : J Public Health Afr

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    Little is known on the impact of HIV-2 infection on HCV viral replication. The aim of the study was to compare HCV prevalence and viral replication based on HIV types in West Africa. A cross-sectional survey was conducted within the IeDEA HIV-2 West Africa cohort from March to December 2012. All HIVinfected adult patients who attended participating HIV clinics during the study period were included. Blood samples were collected and re-tested for HIV type discrimination, HCV serology and viral load. A total of 767 patients were enrolled: 186 HIV-1, 431 HIV-2 and 150 HIV-1&2 dually reactive. At time of sampling, 531 (69.2%) were on ART and median CD4+ cell count was 472/mm(3). Thirty (3.9%, 95% CI 2.7-5.5) patients were anti-HCV positive (4.3% in HIV-1, 4.0% in HIV-1&2 dually reactive and 3.7% in HIV-2; p=0.91). Detectable HCV RNA was identified in 21 (70.0%) patients (100% in HIV-1 and HIV- 1&2 dually reactive vs. 43.8% in HIV-2; p=0.003). Systematic screening should be promoted and performed in this population, since HCV is now potentially curable in sub- Saharan Africa

    « La saletĂ© n’a qu’à descendre » : rapport au corps et expĂ©riences vĂ©cues par les travailleuses du sexe en CĂŽte d’Ivoire (projets ANRS 12361 PrEP-CI et ANRS 12381 PRINCESSE)

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    Objectifs Analyser le rapport au corps de travailleuses du sexe (TS) enquĂȘtĂ©es en CĂŽte d’Ivoire dans la rĂ©gion de San Pedro. Leurs reprĂ©sentations d’un corps situĂ© Ă  la frontiĂšre des sphĂšres intime et professionnelle peut Ă©clairer leurs perceptions et l’acceptabilitĂ© des services de santĂ© qui leur sont proposĂ©s. MatĂ©riels et MĂ©thodes Des entretiens qualitatifs ont Ă©tĂ© rĂ©alisĂ©s, au sein de l’étude transversale PrEP-CI et du projet PRINCESSE qui a suivi (cohorte interventionnelle mono-bras avec offre Ă©largie en santĂ© sexuelle et reproductive, dont PrEP), en 3 vagues (2016, 2019, 2021) auprĂšs de 100 TS, complĂ©tĂ©s par des observations de terrain sur sites. RĂ©sultats La notion de circulation des fluides et son importance dans le maintien d’un "Ă©quilibre" Ă©mergent des entretiens. Certaines TS expriment la crainte que les interventions de santĂ©, et en particulier les prises de sang, puissent affaiblir le corps, induire de la "fatigue", notamment si cela n’est pas contrebalancĂ© par l’ingestion de substances Ă©nergĂ©tiques, comme des boissons sucrĂ©es. Le nombre Ă©levĂ© de tubes de prĂ©lĂšvements sanguins et l’absence de collation (jusque mi 2021) sont mentionnĂ©s comme des freins Ă  l’engagement dans les soins. La notion de circulation renvoie Ă©galement Ă  l’expulsion de la "saletĂ©", comme sont souvent dĂ©finis le sperme ou les rĂšgles. Lors d’une rupture de prĂ©servatif, il n’est pas rare que les TS se "purgent" en nettoyant leur corps par l’ingestion de cola ou des lavements, ce qu’elles perçoivent comme plus efficace que la prise de comprimĂ©s (traitement IST ou post-exposition VIH, pilule du lendemain), qui reste exceptionnelle. Les TS sont souvent rĂ©ticentes Ă  utiliser les injections ou les implants contraceptifs, car les rĂšgles risquent de "rester" plutĂŽt que de "descendre" et d’ĂȘtre Ă©vacuĂ©es. À l’inverse, il s’agit parfois de bloquer la circulation des fluides. Les TS interrogĂ©es se "prĂ©servent" en utilisant des prĂ©servatifs avec leurs clients. Les rapports tarifĂ©s sans prĂ©servatif relĂšvent de l’exception, avec des clients rĂ©guliers ou Ă  des tarifs bien plus Ă©levĂ©s. Sa non-utilisation avec leur partenaire rĂ©gulier permet de diffĂ©rencier relation personnelle et professionnelle. Par ailleurs, la circulation des menstrues peut ĂȘtre temporairement suspendue, par du coton ou de la glace, le temps du travail. La PrEP, mĂ©dicament que l’on prend sans ĂȘtre malade, apparaĂźt pour certaines comme "fatigante" et "inutile", avec le risque de causer un dĂ©sĂ©quilibre dans un corps bien portant, bien qu’elle empĂȘche la maladie de "rentrer dans le corps". Conclusion Ces analyses, qui seront complĂ©tĂ©es dĂ©but 2022 avec une enquĂȘte spĂ©cifique, montrent que les TS ont une approche de leur santĂ© et du soin de soi qui n’est pas forcĂ©ment celle pensĂ©e par l’équipe du projet. Le rapport au corps des TS Ă©claire les rĂ©ticences qu’elles peuvent exprimer quant aux diffĂ©rentes offres de santĂ©, pas toujours perçues comme adaptĂ©es, et explique en partie les freins Ă  l’entrĂ©e et au maintien dans les soins, confirmĂ©s par les donnĂ©es quantitatives

    Hiv Aids (Auckl)

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    Background: Reporting mortality and lost to follow-up (LTFU) by age is essential as older HIV-positive patients might be at risk of long-term effects of living with HIV and/or taking antiretroviral therapy (ART). As age effects might not be linear and might impact HIV outcomes in the oldest more severely, people living with HIV (PLHIV) aged 50-59 years and PLHIV aged >60 years were considered separately. Setting: Seventeen adult HIV/AIDS clinics spread over nine countries in West Africa. Methods: Data were collected within the International Epidemiological Databases to Evaluate AIDS West Africa Collaboration. ART-naive PLHIV-1 adults aged >16 years initiating ART and attending >= 2 clinic visits were included (N=73,525). Age was divided into five groups: 16-29/30-39/40-49/50-59/>= 60 years. The age effect on mortality and LTFU was evaluated with Kaplan-Meier curves and multivariable Cox proportional hazard regressions. Results: At month 36, 5.9% of the patients had died and 47.3% were LTFU. Patients aged >= 60 (N=1,736) and between 50-59 years old (N=6,792) had an increased risk of death in the first 36 months on ART (adjusted hazard ratio=1.66; 95% CI: 1.36-2.03 and adjusted hazard ratio=1.31; 95% CI: 1.15-1.49, respectively; reference: = 60 years old tend to be more often LTFU. Condusion: The oldest PLHIV presented the poorest outcomes, suggesting that the PLHIV aged >50 years old should not be considered as a unique group irrespective of their age. Tailored programs focusing on improving the care services for older PLHIV in Sub-Saharan Africa are clearly needed to improve basic program outcomes

    Virological, serological and clinical outcomes in chronic hepatitis B virus infection: development and validation of the HEPA-B simulation model

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    Objectives Detailed simulation models are needed to assess strategies for prevention and treatment of hepatitis B virus (HBV) infection, the world’s leading cause of liver disease. We sought to develop and validate a simulation model of chronic HBV that incorporates virological, serological and clinical outcomes.Methods We developed a novel Monte Carlo simulation model (the HEPA-B Model) detailing the natural history of chronic HBV. We parameterised the model with epidemiological data from the Western Pacific and sub-Saharan Africa. We simulated the evolution of HBV DNA, ‘e’ antigen (HBeAg) and surface antigen (HBsAg). We projected incidence of HBeAg loss, HBsAg loss, cirrhosis, hepatocellular carcinoma (HCC) and death over 10-year and lifetime horizons. We stratified outcomes by five HBV DNA categories at the time of HBeAg loss, ranging from HBV DNA&lt;300 copies/mL to &gt;106 copies/mL. We tested goodness of fit using intraclass coefficients (ICC).Results Model-projected incidence of HBeAg loss was 5.18% per year over lifetime (ICC, 0.969 (95% CI: 0.728 to 0.990)). For people in HBeAg-negative phases of infection, model-projected HBsAg loss ranged from 0.78% to 3.34% per year depending on HBV DNA level (ICC, 0.889 (95% CI: 0.542 to 0.959)). Model-projected incidence of cirrhosis was 0.29–2.09% per year (ICC, 0.965 (95% CI: 0.942 to 0.979)) and HCC incidence was 0.06–1.65% per year (ICC, 0.977 (95% CI: 0.962 to 0.986)). Over a lifetime simulation of HBV disease, mortality rates were higher for people with older age, higher HBV DNA level and liver-related complications, consistent with observational studies.Conclusions We simulated HBV DNA-stratified clinical outcomes with the novel HEPA-B Model and validated them to observational data. This model can be used to examine strategies of HBV prevention and management

    J Viral Hepat

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    BACKGROUND: It is unknown how past and active hepatitis B virus (HBV) infection affect immunorecovery and mortality in people with HIV who initiate tenofovir-based anti-retroviral therapy (ART). METHODS: Using data collected between 2008- 2015, we studied people with HIV in sub-Saharan Africa initiating immediate ART in the Temprano randomized control trial. We classified participants into HBV groups at ART-initiation: hepatitis B surface antigen (HBsAg)-positive with HBV DNA ≄2000 IU/mL; HBsAg-positive with HBV DNA <2000 IU/ml; isolated HBcAb-positive; resolved infection (HBsAb-positive/HBcAb-positive); and HBV non-immune/vaccinated (HBcAb-). We compared square-root CD4-cell count increases using a mixed-effect, non-linear regression adjusted for age, sex, baseline CD4 cell count, and HIV RNA. We compared all-cause mortality using Bayesian parametric survival regression. RESULTS: Among 879 participants, 24 (2.7%) had HBsAg with high HBV DNA, 76 (8.6%) HBsAg with low HBV DNA, 325 (37.0%) isolated anti-HBcAb, 226 (25.7%) resolved HBV infection, and 228 (25.9%) HBV non-immune/vaccinated. We found no significant difference in CD4 cell increases between the four HBV-infection groups after adjustment (p=0.16). Participants with HBsAg and high HBV DNA had the highest incidence of all-cause mortality [1.9/100 person-years, 95%Credibile Interval (CrI)=1.0-3.4]. By comparison, incidence rates of mortality were reduced by 57% (95%CrI=-79%,-13%), 60% (95%CrI=-82%,-12%), and 66% (95%CrI=-84%,-23%) in those who had isolated anti-HBcAb-positive, resolved HBV infection, and HBV non-immune/vaccinated, respectively. CONCLUSION: Individuals with HIV and past HBV infection or isolated anti-HBcAb-positive serology, much like HBV non-immune/vaccinated, experience lower mortality than those with HBsAg and high HBV DNA. Additional HBV-related management would not be necessary for these individuals

    Tobacco use and its determinants in HIV-infected patients on antiretroviral therapy in West African countries.: Tobacco use in HIV-infected patients in West Africa

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    International audienceBACKGROUND: Tobacco smoking is common in human immunodeficiency virus (HIV) infected patients from industrialised countries. In West Africa, few data concerning tobacco consumption exist. METHODS: A cross-sectional survey of the International Epidemiological Database to Evaluate AIDS (IeDEA) network in West Africa was conducted. Health workers administered a questionnaire assessing tobacco and cannabis consumption among patients receiving antiretroviral treatment. Regular smokers were defined as current smokers who smoked >1 cigarette per day for >or=1 year. RESULTS: Overall, 2920 patients were enrolled in three countries. The prevalence of ever smokers and regular smokers were respectively 46.2% (95%CI 42.8-49.5) and 15.6% (95%CI 13.2-18.0) in men and 3.7% (95%CI 2.9-4.5) and 0.6% (95%CI 0.3-0.9) in women. Regular smoking was associated with being from CĂŽte d'Ivoire or Mali compared to Benin (OR 4.6, 95%CI 2.9-7.3 and 7.7, 95%CI 4.4-13.6), severely impaired immunological status at highly active antiretroviral treatment initiation (OR 1.5, 95%CI 1.1-2.2) and history of tuberculosis (TB; OR 1.8, 95%CI 1.1-3.0). CONCLUSION: There are marked differences in smoking prevalence among these West African countries. This survey approach also provides proof of the association between cigarette smoking and TB in HIV-infected patients, a major public health issue in this part of the world
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