Related Experiment Video
Updated: Jun 3, 2026

Humanized NOD/SCID/IL2rγnull (hu-NSG) Mouse Model for HIV Replication and Latency Studies
Published on: January 7, 2019
CD4+ lymphocyte-based immunologic outcomes of perinatally HIV-infected children during antiretroviral therapy
George K Siberry1, Kunjal Patel, Russell B Van Dyke
1Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA. siberryg@mail.nih.gov
Insights
Antiretroviral treatment interruptions (TI) are common in perinatally HIV-infected youth. During TI, CD4 counts typically decline, but individual variability is high, necessitating further research into predictive factors.
Area of Science:
- Pediatric HIV/AIDS research
- Immunology
- Antiretroviral therapy
Background:
- Perinatally HIV-infected children are transitioning into adolescence.
- Understanding outcomes of antiretroviral treatment (ART) interruption is crucial for managing this population.
Purpose of the Study:
- To assess the characteristics and outcomes of ART interruption (TI) in perinatally HIV-infected children.
- To identify factors associated with CD4 T-lymphocyte count changes during TI.
Main Methods:
- Prospective cohort study of 7- to 16-year-old perinatally HIV-infected children.
- TI defined as ART discontinuation for ≥ 3 months.
- Linear regression analysis to determine factors related to CD4 slope during TI.
Main Results:
- 23% of eligible subjects experienced at least one TI.
- Median CD4% slope was -0.66% per month and CD4 count slope was -12.7 cells/mm³ per month during TI.
- Factors like female sex, higher CD4% at TI, and higher peak viral load before TI showed trends associated with faster CD4% decline.
Conclusions:
- ART interruptions are frequent in perinatally HIV-infected youth.
- CD4 values generally decrease during TI, but with significant inter-individual variability.
- Further investigation is needed to understand factors predicting CD4 slope during TI.
Objective:
To assess the characteristics and outcomes of antiretroviral treatment (ART) interruption (TI) in perinatally HIV-infected children.
Design:
The Adolescent Master Protocol (AMP) of the Pediatric HIV/AIDS Cohort Study is a prospective cohort study that enrolled 7- to 16-year-old perinatally HIV-infected children between 2007 and 2009 from 15 sites in the United States and Puerto Rico.
Methods:
TI was defined as ART discontinuation for ≥ 3 months after ≥ 6 months of continuous ART. Subjects with and without TI were compared. Rates of change (slopes) in CD4 T-lymphocyte (CD4) count and percentage (%) per month during TI were calculated. Factors related to CD4 slope in univariable analyses were included in multivariable linear regression.
Results:
Of 444 eligible AMP subjects, 101 (23%) had at least one TI. Subjects with TI were born in earlier years but were otherwise similar to those without TI. For 81 TI subjects with complete data, the median (range) CD4% and CD4 count slopes were -0.66% per month (-3.54% to +1.34% per month) and -12.7 cells per cubic millimeter per month (-148 cells/mm to +31 cells/mm per month), respectively. On multivariable linear regression, there was a trend for lower CD4% slope to be associated (P < 0.1) with female sex, higher CD4% at TI, and higher peak viral load before TI. Advanced HIV disease stage and numerous ART regimens were more common in TI subjects in the lowest (fastest declining) CD4% slope quartile.
Conclusions:
TIs in perinatally HIV-infected youth are common. During TIs, CD4 values decline on average but with high intersubject variability. Factors predicting CD4 slope during TI need further study.
Related Concept Videos
Immunodeficiency Diseases
There are three main causes of immunodeficiency disorders...
Retrovirus Life Cycles
Pharmacokinetics in Pediatric Patients: Drug Excretion
Development of Immunocompetence
The initial cells that migrate from the fetal thymus settle within the skin and epithelial tissues lining the mouth, digestive tract, and in females, the uterus and vagina. These cells, including skin-based dendritic cells, serve as antigen-presenting cells, playing a key role in T cell activation.
Subsequent T...

