Immunological and Virological Responses to Highly Active Antiretroviral Therapy in HIV-1 Infected Children

Ravinder Singh1, Aparna Mukherjee1, Mohit Singla1

  • 1Department of Pediatrics, All India Institute of Medical Sciences, Room no. 3061A, New Delhi, 110029, India.

Insights

Highly active antiretroviral therapy (HAART) improved immune function in HIV-infected children. However, viral load suppression was less effective, with only 20.2% achieving optimal immuno-virological response after six months.

Area of Science:

  • Pediatrics
  • Immunology
  • Virology

Background:

  • Human immunodeficiency virus (HIV) infection remains a significant health concern in children.
  • Highly active antiretroviral therapy (HAART) is the standard of care for pediatric HIV.
  • Evaluating treatment outcomes is crucial for optimizing pediatric HIV management.

Purpose of the Study:

  • To assess the immunological and virological effects of HAART in HIV-infected children.
  • To determine the proportion of children achieving optimal treatment response at six months.
  • To identify challenges in achieving robust virological suppression.

Main Methods:

  • Retrospective review of medical records of HIV-infected children under 15 years old.
  • Inclusion criteria: initiation of HAART between 2010-2014 with available CD4+ T cell percentage and HIV-1 viral load at baseline and 6 months.
  • Data analysis focused on changes in CD4+ T cell percentage and viral load.

Main Results:

  • Seventy-four children were included; median age was 36 months.
  • After 6 months of HAART, a median increase of 11% in CD4+ T cell percentage was observed.
  • Only 20.2% of children achieved both increased CD4+ T cell percentage (≥15%) and undetectable viral load (<47 copies/ml).

Conclusions:

  • HAART demonstrated effectiveness in improving immunological parameters in HIV-infected children.
  • Virological responses to HAART were suboptimal in a significant proportion of the studied cohort.
  • Further research may be needed to enhance viral suppression strategies in pediatric HIV treatment.
Abstract

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