Impaired CD4+ T-cell and CD4+/CD8+ ratio recovery among people with HIV on antiretroviral therapy: prevalence and risk factors

医学 免疫系统 人类免疫缺陷病毒(HIV) 免疫学 免疫病理学 抗逆转录病毒疗法 西达 病毒性疾病 慢病毒 年轻人 病毒载量 内科学 免疫功能障碍 风险因素 CD4-CD8比值 病毒学 人口 抗体
作者
Layla Al-Yasiri,M. John Gill,Hartmut Krentz,Jaqueline McMillan,Raynell Lang
出处
期刊:AIDS [Lippincott Williams & Wilkins]
标识
DOI:10.1097/qad.0000000000004456
摘要

OBJECTIVE: Antiretroviral therapy (ART) decreases HIV viral replication leading to CD4+ recovery, decreased CD8+ expansion and CD4+/CD8+ ratio recovery. We investigated factors associated with impaired recovery of CD4+ and CD4+/CD8+ ratios among people with HIV (PWH) maintaining HIV viral suppression. DESIGN/METHODS: PWH ≥18 years accessing the Southern Alberta Clinic between 01/01/1998-01/06/2022 entered the study at time of HIV viral suppression (<200 copies/mL). Continuous time-to-event Cox proportional hazard models estimated crude and adjusted hazards ratios (aHR) and 95% confidence intervals for factors associated with recovery of CD4+ count (≥500 cells/mm3) and CD4+/CD8+ ratio (≥1) at 10 years. RESULTS: Over 10 years, 83% of PWH reached a CD4+ count of ≥500 cells/mm3 but only 54% reached a CD4+/CD8+ ratio of ≥1. CD4+ recovery was less common among people diagnosed with HIV >50 years old vs. <30 years old (aHR: 0.59 [0.46-0.77]). Females were more likely to recover both CD4+ (aHR: 1.42[1.18-1.71]) and CD4+/CD8+ ratios (aHR: 1.56[1.25-1.95]) compared with males. Both higher baseline CD4+ counts and CD4+/CD8+ ratios were associated with greater immune recovery. ART regimen at study entry impacted CD4+ but not CD4+/CD8+ ratio recovery. CMV coinfection was associated with reduced CD4+/CD8+ ratio recovery (aHR: 0.47 [0.37-0.62]). CONCLUSIONS: While most PWH with ongoing viral suppression will recover their CD4+ cell counts, recovery of CD4+/CD8+ ratio recovery is less common, indicating ongoing immune dysfunction. Several demographic and clinical factors are associated with impaired immune recovery. Further characterization and understanding of the long-term impact of impaired immune recovery is needed.
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