[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100539368":3},{"organization":4,"outcomesModule":7,"designInfo":45,"detailedDescription":52,"studyPopulation":44,"armGroups":53,"interventions":59,"overallOfficials":44,"centralContacts":65,"locations":75,"responsibleParty":120,"collaborators":122,"id":141,"slug":142,"hasResults":143,"nctId":144,"briefTitle":145,"officialTitle":145,"acronym":146,"eligibilityCriteria":147,"healthyVolunteers":148,"sex":149,"minAge":44,"maxAge":44,"enrollmentInfo":150,"targetDuration":44,"studyType":153,"phases":154,"briefSummary":155,"conditions":156,"keywords":44,"overallStatus":96,"whyStopped":44,"lastUpdateSubmitDate":158,"lastUpdatePostDateStruct":159,"startDateStruct":162,"completionDateStruct":164,"leadSponsor":166,"locationsCount":167},{"fullName":5,"class":6},"ANRS, Emerging Infectious Diseases","OTHER_GOV",{"primaryOutcomes":8,"secondaryOutcomes":25,"otherOutcomes":44},[9,13,15,17,19,21,23],{"measure":10,"description":11,"timeFrame":12},"Level of pro-inflammatory and anti-inflammatory cytokines, chimiokines in the plasma","Measure of sCD14 (µg\u002Fml). Levels of these biomarkers will be compared across all groups.","18 months",{"measure":10,"description":14,"timeFrame":12},"Measure of BAFF using luminex or commercially available ELISA quantification kits. Levels of these biomarkers will be compared across all groups.",{"measure":10,"description":16,"timeFrame":12},"Measure of CXCL13 using luminex or commercially available ELISA quantification kits. Levels of these biomarkers will be compared across all groups.",{"measure":10,"description":18,"timeFrame":12},"Measure of TNF-α (pg\u002Fml). Levels of these biomarkers will be compared across all groups.",{"measure":10,"description":20,"timeFrame":12},"Measure of IL-10 (pg\u002Fml). Levels of these biomarkers will be compared across all groups.",{"measure":10,"description":22,"timeFrame":12},"Measure of IP-10 (pg\u002Fml). Levels of these biomarkers will be compared across all groups.",{"measure":10,"description":24,"timeFrame":12},"Measure of TRAIL (ng\u002Fml). Levels of these biomarkers will be compared across all groups",[26,29,32,35,38,41],{"measure":27,"description":28,"timeFrame":12},"- Humoral response to vaccines against tetanus, pertussis, and viral hepatitis B","Serum concentrations of human IgG antibodies against tetanus-toxoid, pertussis, and viral hepatitis B will be measured using commercially available ELISA quantification kits and results will be given as IU\u002FmL",{"measure":30,"description":31,"timeFrame":12},"- Functional and phenotypic characterization of B and T lymphocytes","Level (cells\u002FμL or percentage) of T and B-cell lymphocytes subpopulations will be assess in blood using flow cytometry. Functional characterization of T and B lymphocytes will be done by cell culture following by cytokine production titration",{"measure":33,"description":34,"timeFrame":12},"- Size of the HIV reservoir","Measure total (copies\u002Fmillion PBMC), integrated (copies\u002Fmillion PBMC), unintegrated (copies\u002Fmillion PBMC) HIV DNA level in Peripheral Blood Mononuclear Cells (PBMC)",{"measure":36,"description":37,"timeFrame":12},"- Residual viremia in perinatally HIV-infected adolescent","Any detectable HIV-RNA below 50 copies\u002FmL",{"measure":39,"description":40,"timeFrame":12},"- Level of HIV plasma p24","Measure plasma level of HIV p24 antigen (fg\u002Fml) using ultrasentsitive technique called Simoa (Single molecule array)",{"measure":42,"description":43,"timeFrame":12},"- HLA phenotype and the KIR genotypes","HLA-B (27 et 57), HLA-B35 ou 53, HLA-C16:01+KIR2DL3+",null,{"allocation":46,"interventionModel":47,"interventionModelDescription":48,"primaryPurpose":49,"observationalModel":44,"timePerspective":44,"maskingInfo":50},"NA","SINGLE_GROUP","Study type: a study nested in the ANRS 12225 - Pediacam III cohort, comprising two phases\n\n* A retrospective phase: case-control study The analyzed data are those collected previously or measured from the already available bio bank, within the framework of the Pediacam III cohort during the primary infection phase before the initiation of HAART, at 6 months after the end of the first series of EPI vaccines, and at 2 years.\n* A prospective phase: cross-sectional study Based on an ad hoc bio bank created for parameters we couldn't measure on the existing bio bank","HEALTH_SERVICES_RESEARCH",{"masking":51,"maskingDescription":44,"whoMasked":44},"NONE","There will be two phases of the study :\n\n* A retrospective phase: case-control study The analyzed data are those collected previously or measured from the already available bio bank, within the framework of the Pediacam III cohort during the primary infection phase before the initiation of HAART, at 6 months after the end of the first series of EPI vaccines, and at 2 years.\n* A prospective phase: cross-sectional study Based on an ad hoc bio bank created for parameters we couldn't measure on the existing bio bank",[54],{"label":55,"type":56,"description":44,"interventionNames":57},"Children enrolled in Pediacam III ANRS12225 cohort","OTHER",[58],"Biological: Blood sampling",[60],{"type":61,"name":62,"description":63,"armGroupLabels":64,"otherNames":44},"BIOLOGICAL","Blood sampling","Blood samples collected from children followed in the Pediacam III ANRS12225 cohort",[55],[66,71],{"name":67,"role":68,"phone":69,"phoneExt":44,"email":70},"Mathurin C Tejiokem, Doctor","CONTACT","00237222231803","tejiokem@pasteur-yaounde.org",{"name":72,"role":68,"phone":73,"phoneExt":44,"email":74},"Albert Faye, Doctor","0033140035361","albert.faye@rdb.ap-hop-paris.fr",[76,94,109],{"facility":77,"status":78,"city":79,"state":44,"zip":80,"country":81,"countryCode":82,"cosmosGeoPoint":83,"geoPoint":88,"contacts":89},"Hôpital de Jour - Hôpital Laquintinie de Douala","NOT_YET_RECRUITING","Douala","4035","Cameroon","CM",{"type":84,"coordinates":85},"Point",[86,87],9.70428,4.04827,{"lat":87,"lon":86},[90],{"name":91,"role":68,"phone":92,"phoneExt":44,"email":93},"Astrid Moukoko, Dr","00237699 14 90 47","astridmoukoko@gmail.com",{"facility":95,"status":96,"city":97,"state":44,"zip":98,"country":81,"countryCode":82,"cosmosGeoPoint":99,"geoPoint":103,"contacts":104},"Unité Pédiatrique de Jour - Centre Mère et Enfant de la Fondation Chantal Biya","RECRUITING","Yaoundé","1274",{"type":84,"coordinates":100},[101,102],11.51667,3.86667,{"lat":102,"lon":101},[105],{"name":106,"role":68,"phone":107,"phoneExt":44,"email":108},"Francis A Ndongo, Dr","00237 677 33 00 55","atebfranc@gmail.com",{"facility":110,"status":96,"city":97,"state":44,"zip":111,"country":81,"countryCode":82,"cosmosGeoPoint":112,"geoPoint":114,"contacts":115},"Service de Pédiatrie - Centre Hospitalier d'Essos","5777",{"type":84,"coordinates":113},[101,102],{"lat":102,"lon":101},[116],{"name":117,"role":68,"phone":118,"phoneExt":44,"email":119},"Suzie T Ndiang, Dr","00237 679 53 86 71","ndiangsuzie@yahoo.fr",{"type":121,"investigatorFullName":44,"investigatorTitle":44,"investigatorAffiliation":44,"oldNameTitle":44,"oldOrganization":44},"SPONSOR",[123,125,127,129,131,134,137,139],{"name":124,"class":56},"Centre Pasteur du Cameroun",{"name":126,"class":56},"Centre Mère et Enfant de la Fondation Chantal Biya",{"name":128,"class":56},"Centre Hospitalier D'essos",{"name":130,"class":56},"Hospital General De Douala",{"name":132,"class":133},"CH Orléans","UNKNOWN",{"name":135,"class":136},"Institut Pasteur","INDUSTRY",{"name":138,"class":56},"Hopital Universitaire Robert-Debre",{"name":140,"class":56},"Université Paris-Sud","100539368","negative-serology-by-immunoenzymatic-test-eia-in-hiv-infected-children-treated-early-with-antiretroviral-in-the-anrs-pediacam-study-pathophysiological-mechanisms-100539368",false,"NCT06302933","Negative Serology by Immunoenzymatic Test (EIA) in HIV-infected Children Treated Early With Antiretroviral in the ANRS-Pediacam Study: Pathophysiological Mechanisms","PediacamNEG","Inclusion Criteria:\n\nCase control study\n\n* Children included and followed in the ANRS 12225 study - Pediacam III\n* Having plasma samples in the bio bank during the above-mentioned periods Case:children with at least one negative HIV serology made by ELISA, permanent or transientduring follow-up.\n\nControl (4 groups)\n\n* HIV-infected children with positive serology and viral load (VL) \\\u003C400 copies \u002Fml\n* HIV-infected children with positive serology and VL ≥400 copies \u002F ml\n* HIV-uninfected children born to HIV-positive mothers\n* HIV-uninfected children born to HIV-uninfected mothers Selection of cases and controls will be matched on gestational age (premature \\\u003C37, term ≥37 weeks) and year of birth (2007-2008 and 2009-2010).\n\nCross sectional study Inclusion criteria\n\n* All children still followed in the ANRS - Pediacam III cohort\n* Written consent of one of the parents or the guardian and assent of the child if aged ≥ 11 years and complete disclosure of HIV statusfor infected children for participation to the study.\n\nExclusion Criteria:\n\n* Refusal by one of the parents or the guardian for the child's participation in the study\n* No assent of the child (if aged ≥ 11 years and with complete disclosure of HIV status, for infected children)",true,"ALL",{"count":151,"type":152},451,"ESTIMATED","INTERVENTIONAL",[46],"The objective of the study is to identify the pathophysiological mechanisms responsible for the induction and maintenance of negative serologies by EIA tests in HIV-infected children treated early with HAART in the ANRS 12225-Pediacam III cohort in Cameroon\n\nThe hypothesis of better control of HIV infection through interactions between immunological, viral, and genetic factors was made to build the following objectives:\n\n* Immunological aspect: lack of humoral response or immune activation\n* Virological aspect: Reduced HIV reservoir size\n* Determine the HLA phenotype in the different groups of children included and the KIR genotypes.",[157],"HIV Infections","2025-01-28",{"date":160,"type":161},"2025-01-30","ACTUAL",{"date":163,"type":161},"2024-05-02",{"date":165,"type":152},"2025-08-30",{"name":5,"class":6},3]