HIV Immune Reconstitution Inflammatory Syndrome in Uganda
HIV Immune Reconstitution Inflammatory Syndrome in Uganda
批准号:
7648233
负责人:
Paul R Bohjanen
金额:
$7.55万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-07-01 至 2010-06-30
关键词:
Acquired Immunodeficiency SyndromeAfricaAfrica South of the SaharaAnti-Retroviral AgentsApplications GrantsBiological AssayBiological MarkersBlood TestsBlood specimenClinicalClinical ResearchCohort StudiesComplicationCryptococcal MeningitisDataDevelopmentDiagnosisDiagnosticEnrollmentEnzyme-Linked Immunosorbent AssayEventExhibitsFunctional disorderFundingFutureGene ExpressionGene Expression ProfileGene Expression ProfilingGoalsGrantHIVHIV InfectionsImmuneImmune systemImmunologicsImmunotherapyIncidenceIndividualInfectionInflammatoryInflammatory ResponseMinnesotaMorbidity - disease rateOutcomePathogenesisPathologicPathway interactionsPatient MonitoringPatientsPilot ProjectsRNAReactionResearch Project GrantsResourcesRiskRisk FactorsSamplingSeveritiesSyndromeTimeTranslational ResearchTreatment ProtocolsUgandaUniversitiesWhole Bloodantiretroviral therapybasecompliance behaviorexperienceimprovedinsightmortalityperipheral bloodprogramspublic health relevancereconstitutionresponsesuccess
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): HIV immune reconstitution inflammatory syndrome (IRIS) is a newly recognized complication of anti- retroviral therapy (ART) whereby a portion of patients with advanced HIV who initiate ART subsequently experience paradoxical clinical worsening due to exaggerated inflammatory responses to occult, latent, or previously treated infections. HIV IRIS has emerged as a frequent complication of ART in sub-Saharan Africa. Our long term goal is to understand the pathogenesis of IRIS so we can develop optimized ART regimens to minimize the morbidity and mortality associated with IRIS in resource limited regions. We are currently performing a study in HIV-infected patients in Uganda as they initiate ART to better understand the impact of IRIS in Sub-Saharan Africa. The goals of the ongoing study are to evaluate the incidence, severity and clinical features of IRIS and to determine if HIV-infected Ugandan patients who develop IRIS have worse clinical outcomes compared to patients who do not develop IRIS. We are prospectively following 100 HIV-infected Ugandan patients for one year after they initiate ART. Of these, 50 patients have no active OI at time of ART initiation, and 50 patients have a diagnosis of cryptococcal meningitis within the previous 2 months. In addition to determining the incidence, severity, and clinical features of IRIS after initiation of ART in these patients, we will also determine whether the development of an IRIS event has a negative effect on ART compliance and whether this impacts treatment success. For this R03 grant application, we plan to use blood specimens obtained from patients in our ongoing cohort study to evaluate immune activation. The specific aim is to identify predictive and diagnostic biomarkers of IRIS by comparing immune activation in the peripheral blood of patients who develop IRIS versus those who do not develop IRIS after initiation of ART. We will prospectively collect whole blood RNA before and after initiation of ART and will use Affymetrix microarrays to compare immune activation gene expression between patients who develop IRIS and patients who do not develop IRIS. In this way, we will identify specific biomarkers associated with IRIS that are diagnostic of IRIS or predictive of future IRIS. A goal is to identify biomarkers that can be adapted into simple, inexpensive assays, such as real time PCR or ELISA, that can be used clinically to diagnose IRIS or monitor patients at risk for IRIS. The identification of biomarkers of IRIS will also provide important insight into the immune activation pathways that underlie the pathophysiology of IRIS. PUBLIC HEALTH RELEVANCE: HIV immune reconstitution inflammatory syndrome (IRIS) has emerged in sub-Saharan Africa as an important complication to antiretroviral therapy to treat HIV infection. Patients who develop IRIS exhibit clinical worsening due to inflammatory reactions that occur as their immune systems improve after starting antiretroviral therapy. The goal of this study is to develop clinical blood tests that could be used to diagnose IRIS and predict patients who are at risk for its development before they become ill.
期刊论文(2)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1128/mbio.00196-12
发表时间:
2012
期刊:
mBio
影响因子:
6.4
作者:
[Wiesner DL, Moskalenko O, Corcoran JM, McDonald T, Rolfes MA, Meya DB, Kajumbula H, Kambugu A, Bohjanen PR, Knight JF, Boulware DR, Nielsen K]
通讯作者:
Nielsen K
Immunopathogenesis of immune reconstitution disease in HIV patients responding to antiretroviral therapy.
对抗逆转录病毒疗法反应的HIV患者免疫重建疾病的免疫发病发生。
DOI:
10.1097/coh.0b013e328302ebbb
发表时间:
2008-07
期刊:
Current opinion in HIV and AIDS
影响因子:
4.1
作者:
[Kestens L, Seddiki N, Bohjanen PR]
通讯作者:
Bohjanen PR
Etiology and Outcomes of Meningitis in Rural, Northern Uganda
-
批准号:10543219
-
项目类别:
-
资助金额:$18.98万
-
财政年份:2022
-
负责人:Paul R Bohjanen
-
依托单位:
Etiology and Outcomes of Meningitis in Rural, Northern Uganda
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批准号:10693970
-
项目类别:
-
资助金额:$16.26万
-
财政年份:2022
-
负责人:Paul R Bohjanen
-
依托单位:
Outcomes of Cryptococcal Meningitis in Uganda
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批准号:8701228
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项目类别:
-
资助金额:$20.35万
-
财政年份:2011
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负责人:Paul R Bohjanen
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依托单位:
Outcomes of Cryptococcal Meningitis in Uganda
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批准号:8262257
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项目类别:
-
资助金额:$20.35万
-
财政年份:2011
-
负责人:Paul R Bohjanen
-
依托单位:
Outcomes of Cryptococcal Meningitis in Uganda
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批准号:8337205
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项目类别:
-
资助金额:$20.35万
-
财政年份:2011
-
负责人:Paul R Bohjanen
-
依托单位:
Outcomes of Cryptococcal Meningitis in Uganda
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批准号:8511559
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项目类别:
-
资助金额:$20.35万
-
财政年份:2011
-
负责人:Paul R Bohjanen
-
依托单位:
Impact of HIV and HIV therapy on the Etiology and Outcome of Meningitis in Uganda
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批准号:7920491
-
项目类别:
-
资助金额:$14.55万
-
财政年份:2010
-
负责人:Paul R Bohjanen
-
依托单位:
Novel Regulators of T Cell mRNA Decay
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批准号:8104636
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项目类别:
-
资助金额:$1.49万
-
财政年份:2010
-
负责人:Paul R Bohjanen
-
依托单位:
Impact of HIV and HIV therapy on the Etiology and Outcome of Meningitis in Uganda
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批准号:8073433
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项目类别:
-
资助金额:$13.01万
-
财政年份:2010
-
负责人:Paul R Bohjanen
-
依托单位:
Novel Regulators of T Cell mRNA Decay
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批准号:7792496
-
项目类别:
-
资助金额:$32.9万
-
财政年份:2008
-
负责人:Paul R Bohjanen
-
依托单位:
HIV Immune Reconstitution Inflammatory Syndrome in Uganda
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批准号:7552491
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项目类别:
-
资助金额:$7.55万
-
财政年份:2008
-
负责人:Paul R Bohjanen
-
依托单位:
Novel Regulators of T Cell mRNA Decay
-
批准号:7366888
-
项目类别:
-
资助金额:$33.24万
-
财政年份:2008
-
负责人:Paul R Bohjanen
-
依托单位:
Novel Regulators of T Cell mRNA Decay
-
批准号:7582443
-
项目类别:
-
资助金额:$33.24万
-
财政年份:2008
-
负责人:Paul R Bohjanen
-
依托单位:
Novel Regulators of T Cell mRNA Decay
-
批准号:8035934
-
项目类别:
-
资助金额:$32.57万
-
财政年份:2008
-
负责人:Paul R Bohjanen
-
依托单位:
mRNA Decay in T Lymphocyte Activation
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批准号:7172448
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项目类别:
-
资助金额:$32.45万
-
财政年份:2006
-
负责人:Paul R Bohjanen
-
依托单位:
Regulation of T Lymphocyte mRNA Degradation
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批准号:6897192
-
项目类别:
-
资助金额:$10.78万
-
财政年份:2002
-
负责人:Paul R Bohjanen
-
依托单位:
Regulation of T Lymphocyte mRNA Degradation
-
批准号:7072744
-
项目类别:
-
资助金额:$10.78万
-
财政年份:2002
-
负责人:Paul R Bohjanen
-
依托单位:
Regulation of T Lymphocyte mRNA Degradation
-
批准号:6647594
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项目类别:
-
资助金额:$10.78万
-
财政年份:2002
-
负责人:Paul R Bohjanen
-
依托单位:
Regulation of T Lymphocyte mRNA Degradation
-
批准号:6507670
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项目类别:
-
资助金额:$10.78万
-
财政年份:2002
-
负责人:Paul R Bohjanen
-
依托单位:
Regulation of T Lymphocyte mRNA Degradation
-
批准号:6751501
-
项目类别:
-
资助金额:$10.78万
-
财政年份:2002
-
负责人:Paul R Bohjanen
-
依托单位:
海外基金