Abstract

BackgroundThe immune reconstitution after initiation of highly active antiretroviral therapy (HAART) among HIV-infected individuals substantially affects patients’ prognosis. However, the dynamic characteristics and predictors of reconstitution outcome remain unclear.MethodsIn this study, the HIV/AIDS patients with sustained virological suppression (viral load < 50 copies/ml) after HAART were enrolled. The patients were subgrouped into immunological non-responders (INRs) (< 200 cells/μl), immunological inadequate responders (IIRs) (200 ~ 500 cells/μl) and immunological responders (IRs) (> 500 cells/μl) according to the CD4 cell count after two-year HAART. The immune reconstitution data based on the CD4+ and CD8+ cell counts with 8-year follow-up were collected for analysis.ResultsThe CD4+ cell counts in the immunological responders (IRs) were significantly higher than in the immunological non-responders (INRs) and immunological inadequate responders (IIRs) (P < 0.001). The overall CD4+ cell count and CD4/CD8 ratio in the IRs increased faster than the IIRs and INRs. The CD4+ cell count growth at 0.5 year and 1 year after HAART in the IRs was significantly higher than the IIRs and INRs. The ROC curve demonstrated that 1 year CD4+ cell count had the highest predictive value, with the best cut-off value of 188 cells/μl, the predictive sensitivity was 81.0%, the predictive specificity was 85.2%, false positive rate was 14.8%, false negative rate was 19.0%, positive predictive value (IR) was 63.0%, negative predictive value (INR) was 93.5%.ConclusionsTaken together, our findings suggest that early initiation of HAART can reduce the immune reconstitution failure. The combination of baseline CD4+ cell count and baseline CD4/CD8 ratio may serve as a valid predictor of immune reconstitution prognosis after HAART.

Highlights

  • The immune reconstitution after initiation of highly active antiretroviral therapy (HAART) among HIVinfected individuals substantially affects patients’ prognosis

  • Immune reconstitution following HAART is characterized by distinct cluster of differentiation 4 (CD4)+ and cluster of differentiation 8 (CD8)+ T cell dynamics, often displaying dichotomist trends according to disease stage [3, 4]

  • According to the CD4 counts of two-year ART, the patients were subgrouped into immunological non-responders (INRs) (< 200 cells/μl), immunological inadequate responders (IIRs) (201 ~ 500 cells/μl) and immunological responders (IRs) (> 500 cells/μl) according to the CD4 cell count after two-year HAART

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Summary

Introduction

The immune reconstitution after initiation of highly active antiretroviral therapy (HAART) among HIVinfected individuals substantially affects patients’ prognosis. The combination antiretroviral therapy (cART), called highly active antiretroviral therapy (HAART), has substantially changed the lives of HIV/AIDS patients [1]. Immune reconstitution following HAART is characterized by distinct CD4+ and CD8+ T cell dynamics, often displaying dichotomist trends according to disease stage [3, 4]. The dynamics of immune reconstitution under long-term HAART varies among different people and regions, and the mechanisms involved remain unclear. The thymus output affects the immune reconstitution, the enhanced thymus output could benefit HIV/ AIDS patients at late stage [6]. The naïve CD4+ cell count is the optimal reference index in prognosis of immune reconstitution [6].

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