Immunophenotyping characteristics and clinical outcome of COVID-19 patients treated with azvudine during the Omicron surge

Front Immunol. 2024 Nov 25:15:1465238. doi: 10.3389/fimmu.2024.1465238. eCollection 2024.

Abstract

Background: Little is known about immunophenotyping characteristics and clinical outcomes of COVID-19 patients treated with azvudine during the Omicron variant surge.

Methods: This study enrolled patients diagnosed with COVID-19 from December 2022 to February 2023. The primary outcome was defined as all-cause mortality, along with a composite outcome reflecting disease progression. The enrolled patients were followed for a period of 60 days from their admission.

Results: A total of 268 COVID-19 patients treated with azvudine were enrolled in this retrospective study. The study found that the counts of lymphocyte subsets were significantly reduced in the composite outcome and all-cause mortality groups compared to the non-composite outcome and discharge groups (all p < 0.001). Correlation analysis revealed a negative association between lymphocyte subsets cell counts and inflammatory markers levels. The receiver operating characteristic (ROC) curve analysis identified low CD4+ T cell count as the most significant predictor of disease progression and all-cause mortality among the various lymphocyte subsets. Additionally, both the Kaplan-Meier curve and multivariate regression analysis demonstrated that low CD4+ T cell count level (< 156.00 cells/μl) was closely associated with all-cause mortality in COVID-19 patients treated with azvudine.

Conclusions: A low CD4+ T cell count may serve as a significant predictive indicator for identifying COVID-19 patients receiving azvudine treatment who are at an elevated risk of experiencing adverse outcomes. These findings may offer valuable insights for physicians in optimizing the administration of azvudine.

Keywords: CD4+ T cell; COVID-19; azvudine; lymphocyte subsets; mortality.

MeSH terms

  • Adult
  • Aged
  • Antiviral Agents / therapeutic use
  • COVID-19 Drug Treatment*
  • COVID-19* / immunology
  • COVID-19* / mortality
  • Disease Progression
  • Female
  • Humans
  • Immunophenotyping*
  • Lymphocyte Count
  • Male
  • Middle Aged
  • Retrospective Studies
  • SARS-CoV-2* / immunology
  • Treatment Outcome

Substances

  • Antiviral Agents

Supplementary concepts

  • SARS-CoV-2 variants

Grants and funding

The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This work was supported by the Science and Technology Program of Yantai City, Grant/Award Number: 2020YD024.