Assessment of HIV-1-Related Oral Mucosal Disease and Use of Saliva in Measuring HIV-1 Viral Load
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 328
- 试验地点
- 6
- 主要终点
- Presumptive clinical diagnoses of oral mucosal diseases
研究概览
简要总结
The mouth may play an important part in monitoring HIV progression. Mucosal lesions of the mouth are often the first sign of infection and their development in already diagnosed individuals indicates disease progression. In addition, saliva may provide a non-invasive way to track viral load. The purpose of this study is to establish standardized practices for examining the mouth and identifying oral mucosal lesions as well as to establish a correlation of viral load with HIV particles found in saliva.
详细描述
The oral cavity has been found to play an important role in monitoring the progression of HIV infection. The occurrence of specific lesions, mainly oral candidiasis and hairy leukoplakia, is strongly associated with a low CD4 cell count and a higher plasma viral load. Furthermore, even though the prevalence of specific oral lesions like candidiasis, hairy leukoplakia, and Kaposi sarcoma (KS) has been found to be lower among patients on highly active antiretroviral therapy (HAART), other oral lesions such as warts have been found to be more prevalent in this population. In addition, saliva has been shown to harbor viral particles, antibodies, and cytokines, and may represent an easily and noninvasively collected specimen for various diagnostic assays, including early diagnosis of HIV. The purpose of this study is to establish a set of standardized practices for examining and diagnosing oral mucosal lesions and to establish a correlation between the amount of HIV found in the saliva with viral load.
Participants in this study will attend only one screening visit and study visit and will be assigned to one of four groups based on viral load and CD4 count. Group A will consist of participants who have a CD4 count of 200 cells/mm3 or less and a viral load greater than 1000 copies/ml. Group B will be made up of participants who have a CD4 count of 200 cells/mm3 or less and a viral load of 1000 copies/ml or less. Group C participants will have a CD4 count that is greater than 200 cells/mm3 and a viral load that is greater than 1000 copies/ml. Participants making up Group D will have a CD4 count that is greater than 200 cells/mm3 and a viral load that is 1000 copies/ml or less.
All participants will have a medical history taken and blood collected as well as performing a throat wash collection and whole saliva collection. In addition, two oral exams will be performed at the study visit.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Cross Sectional
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •HIV-1 infection, as documented by any rapid test or licensed ELISA test kit and confirmed by Western blot, HIV-1 culture, HIV-1 antigen, plasma HIV-1 RNA, or a second antibody test by a method other than ELISA
- •CD4+ cell count obtained ≤ 60 days prior to study entry
- •Plasma HIV-1 RNA levels obtained ≤ 60 days prior to study entry
- •If receiving ART, participants must be on same ART regimen for at least 12 weeks immediately prior to study entry
- •If study participants are not currently on an ART regimen, they must have not discontinued ART therapy within 30 days prior to study entry
- •Ability and willingness of study participant or legal guardian/representative to provide informed consent
排除标准
- •History of head and/or neck radiation secondary to malignancy
- •History of any HIV-1 therapeutic related vaccines
- •Use of any systemic anti-fungal in the 90 days prior to entry
结局指标
主要结局
Presumptive clinical diagnoses of oral mucosal diseases
时间窗: At study visit
Candida CFU level as measured in CFU/mL of throat wash solution.
时间窗: At study visit
HIV-1 viral load in throat wash.
时间窗: At study visit
HIV-1 viral load in plasma
时间窗: At study visit
次要结局
- Prevalence of HIV-1 related oral mucosal lesions(At study visit)
- KSHV DNA viral load in throat wash(At study visit)
- Antifungal resistance as measured by MIC(At study visit)
- HSV-1 DNA viral load in throat wash(At study visit)
- CMV DNA load in throat wash(At study visit)
- Oral candidal genotypes(At study visit)
- EBV DNA viral load in throat wash(At study visit)