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Aging, trends in CD4+/CD8+ cell ratio, and clinical outcomes with persistent HIV suppression in a dynamic cohort of ambulatory HIV patients

Supporting Files
File Language:
English


Details

  • Alternative Title:
    AIDS
  • Personal Author:
  • Corporate Authors:
  • Description:
    Background:

    Age blunts CD4+ lymphocyte cell count/μl (CD4+) improvements observed with antiretroviral therapy (ART)-induced viral suppression among people with HIV (PWH). Prolonged viral suppression reduces immune dysregulation, reflected by rising CD4+/CD8+ ratios (CD4+/CD8+). We studied CD4+/CD8+ over time to determine whether it predicts risk for select comorbidities and mortality among aging PWH with viral suppression.

    Methods:

    We studied HIV Outpatient Study (HOPS) participants prescribed ART during 2000–2018 who achieved a viral load less than 200copies/ml on or after 1 January 2000, and remained virally suppressed at least 1 year thereafter. We modeled associations of CD4+/CD8+ with select incident comorbidities and all-cause mortality using Cox regression and controlling for demographic and clinical factors.

    Results:

    Of 2480 eligible participants, 1145 (46%) were aged less than 40 years, 835 (34%) 40–49 years, and 500 (20%) ≥ 50 years. At baseline, median CD4+/CD8+ was 0.53 (interquartile range: 0.30–0.84) and similar among all age groups (P = 0.18). CD4+/CD8+ values and percentage of participants with CD4+/CD8+ at least 0.70 increased within each age group (P < 0.001 for all). CD4+/CD8+ increase was greatest for PWH aged less than 40 years at baseline. In adjusted models, most recent CD4+/CD8+less than 1.00 and less than 0.70 were independently associated with higher risk of non-AIDS cancer and mortality, respectively.

    Conclusion:

    Pretreatment immune dysregulation may persist as indicated byCD4+/CD8+ less than 0.70. Persistent viral suppression can improve immune dysregulation over time, reducing comorbidity, and mortality risk. Monitoring CD4+/CD8+ among ART-treated PWH with lower values provide a means to assess for mortality and comorbidity risk.

  • Subjects:
  • Keywords:
  • Source:
    AIDS. 36(6):815-827
  • Pubmed ID:
    35013081
  • Pubmed Central ID:
    PMC11004734
  • Document Type:
  • Funding:
  • Volume:
    36
  • Issue:
    6
  • Collection(s):
  • Main Document Checksum:
    urn:sha256:9b1778b3dc6767b7c5baec8fab6d2144a630aab5eba75bdd9c4e8b9eeebe4cee
  • Download URL:
  • File Type:
    Filetype[PDF - 1.59 MB ]
File Language:
English
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